Recall events
/
Event 98239
Event summary
Timeline bucket December 26, 2025
Product types Drug
Classifications Class II
Statuses Ongoing
Recalling firm wording GOLD STAR DISTRIBUTION INC
Dossier provenance
Source snapshots represented here
openFDA Drug Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
Complete imported group
Every recalled product in this event
27 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
drug · product 1 of 27
Advil a) Ibuprofen, Dispenser Pack, 2 tablet packets in box containing 50 individual packets, UPC: 305730154895; b) PM, Ibuprofen, Dispenser Pack, 2 Caplet packets in box containing 50 packets, UPC: 305730164559
D-0261-2026
Recall number D-0261-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unkown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[370]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 27
Aleve 1's, 60 CT
D-0262-2026
Recall number D-0262-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[360]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 27
Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932
D-0263-2026
Recall number D-0263-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[344]
FDA event record
· Exact recall-number query on openFDA
drug · product 4 of 27
Benadryl, 25'S 2PK Box, UPC 815556020316
D-0264-2026
Recall number D-0264-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[412]
FDA event record
· Exact recall-number query on openFDA
drug · product 5 of 27
Bayer 2Pk- 25 CT
D-0265-2026
Recall number D-0265-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[407]
FDA event record
· Exact recall-number query on openFDA
drug · product 6 of 27
Claritin, 20 Count, UPC: 655708016305
D-0266-2026
Recall number D-0266-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[342]
FDA event record
· Exact recall-number query on openFDA
drug · product 7 of 27
DAYQUIL COLD & FLU, 32CT/2PK
D-0267-2026
Recall number D-0267-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[343]
FDA event record
· Exact recall-number query on openFDA
drug · product 8 of 27
LIQUID DAYQUIL 12/8oz
D-0268-2026
Recall number D-0268-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[388]
FDA event record
· Exact recall-number query on openFDA
drug · product 9 of 27
EXCEDRIN 2'S DISP.- 30 CT
D-0269-2026
Recall number D-0269-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[368]
FDA event record
· Exact recall-number query on openFDA
drug · product 10 of 27
EXCEDRIN MIGRAINE 2'S- 25 CT
D-0270-2026
Recall number D-0270-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[355]
FDA event record
· Exact recall-number query on openFDA
drug · product 11 of 27
MOTRIN 2'S DISP.- 50CT
D-0271-2026
Recall number D-0271-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[392]
FDA event record
· Exact recall-number query on openFDA
drug · product 12 of 27
LIQUID NYQUIL a) regular, 12/8oz; b) cherry, 12/8oz
D-0272-2026
Recall number D-0272-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[391]
FDA event record
· Exact recall-number query on openFDA
drug · product 13 of 27
NYQUIL COLD & FLU -32CT/2PK
D-0273-2026
Recall number D-0273-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[367]
FDA event record
· Exact recall-number query on openFDA
drug · product 14 of 27
CHILDREN NYQUIL, COLD&FLU, BERRY, 8oz, 12ct
D-0274-2026
Recall number D-0274-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[369]
FDA event record
· Exact recall-number query on openFDA
drug · product 15 of 27
PEPTO BISMOL 32CT
D-0275-2026
Recall number D-0275-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[339]
FDA event record
· Exact recall-number query on openFDA
drug · product 16 of 27
PEPCID COMPLETE - 25CT
D-0276-2026
Recall number D-0276-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[372]
FDA event record
· Exact recall-number query on openFDA
drug · product 17 of 27
TYLENOL a) 500 MG., 2'S DISPLAY, 50CT; b) COLD & FLU, 25CT/2S; c) COLD & FLU SEVERE, 2PK, 50CT; d) PM, 50CT; e) SINUS SEVERE, 2PK, 50CT
D-0277-2026
Recall number D-0277-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[361]
FDA event record
· Exact recall-number query on openFDA
drug · product 18 of 27
Halls Cough Drops a) BAGS, MENTHOL, 12CT; b) BAGS, HONEY LEM, 12CT; c) BAGS, DEFENSE CITRUS, 12CT; d) BAGS, CHERRY, 12CT; e) M. CHERRY, 20 STK; f) BRAZIL, Cherry, 21CT/27.5G; f) LEMON. HONEY, 20CT #1180E; g) LIME FRESH, 20CT, #1182; h) MENTHOL BLUE, 20CT, #1180A; i) BRAZIL, Menthol, 21CT/27.5G, j) M . STRAWBERRY, 20 STK; k) DEFENSE, VITAMIN C, 20CT, #1181
D-0278-2026
Recall number D-0278-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[414]
FDA event record
· Exact recall-number query on openFDA
drug · product 19 of 27
TUMS a) Assorted, 12 Ct.; b) Extra Strength (EX) Assorted Berries, 12-count #1194A *05/27; c)Extra Strength (EX) Assorted Fruit, 12-count, #1194C *03/27
D-0279-2026
Recall number D-0279-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[356]
FDA event record
· Exact recall-number query on openFDA
drug · product 20 of 27
Swan, White Clear Alcohol, 50%, 16oz, 12 count
D-0280-2026
Recall number D-0280-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[362]
FDA event record
· Exact recall-number query on openFDA
drug · product 21 of 27
Personal Care, Ice Gel, 8oz, 12 count, UPC 048155903463
D-0281-2026
Recall number D-0281-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[365]
FDA event record
· Exact recall-number query on openFDA
drug · product 22 of 27
Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148
D-0282-2026
Recall number D-0282-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[364]
FDA event record
· Exact recall-number query on openFDA
drug · product 23 of 27
Personal Care, Vaporizing Chest Rub, 4 oz, 12 count, UPC 048155903319
D-0283-2026
Recall number D-0283-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[331]
FDA event record
· Exact recall-number query on openFDA
drug · product 24 of 27
LUCKY ICE, Cool Mouthwash, Alcohol Free, 16.9oz, 12CT, UPC: 808829108989
D-0284-2026
Recall number D-0284-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[380]
FDA event record
· Exact recall-number query on openFDA
drug · product 25 of 27
Petroleum jelly: a) Vaseline Petroleum Jelly, 1.75, 12CT, UPC: 6001085120946; b) Vaseline Men Cooling Petroleum Jelly, 100ML, 12CT, UPC: 60022141; c) Vaseline Vitamin E, Petroleum Jelly, 100ML, 12CT, UPC: 6001085121028; MEN FRESH PETROLEUM JELLY, 100ML, 12CT, UPC: 60022127; d) Lucky Petroleum Jelly, 6 OZ, 12 PK, UPC: 808829081466;048155903562; e) Lucky Petroleum Jelly, COCOA, 6oz, 12ct, UPC: 808829081572, 048155922150; f) Personal Care, CREAMY PETROLEUM JELLY, 4.5oz, 12CT, UPC: 048155908642; g) Personal Care, CREAMY COCOA PETROLEUM JELLY, 4.5oz, 12CT, UPC: 048155922242; h) SOFTEE, PETROLEUM JELLY, 5oz, 12CT, UPC: 096002007208
D-0285-2026
Recall number D-0285-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unknown
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[359]
FDA event record
· Exact recall-number query on openFDA
drug · product 26 of 27
Deodorant: a) Axe, Body Spray, Wild Spice, 6CT, 150ML, UPC: 600108736469; b) LUCKY MENS STICK DEODORANT, SPRING FRESH, 24CT, 2.5 OZ, UPC: 808829111668; c) LUCKY MENS STICK DEODORANT, FRESH COMFORT, 24CT, 1.6 OZ, UPC: 808829089103; d) LADY DEODORANT, CHERRY BLOSSOSM, 24CT, 1.8oz, UPC: 048155921092; e) AXE, BODY SPRAY, APOLLO, 6CT, 150ML; f) AXE, BODY SPRAY, BLACK, 6CT, 150ML; g) AXE, BODY SPRAY, DARK TEMPTATION, 6CT, 150ML; h) AXE, BODY SPRAY, GOLD, 6CT, 150ML; i) AXE, BODY SPRAY, EXCITE, 6CT, 150ML; j) AXE, BODY SPRAY, ICE CHILL, 6CT, 150ML; k) AXE, BODY SPRAY, MUSK, 6CT, 150ML; l) AXE, DEODORANT SPRAY, ADRENALIN, 6CT, 150ML
D-0286-2026
Recall number D-0286-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[335]
FDA event record
· Exact recall-number query on openFDA
drug · product 27 of 27
Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct; UPC: 035000511065; b) COLGATE, TOOTHPASTE, Regular, 2.5oz, 24ct, UPC: 035000511058; c) COLGATE, TOOTHPASTE, TRIPLE, 2.5oz, 24ct, UPC: 035000512109; d) COLGATE, TOOTHPASTE, MINT ZING, 24CT, 2.5oz, UPC: 035000744609; COLGATE, MAXFRESH, SPICY FRESH, RED TOOTH PASTE, 72CT, 150G; e) CREST, TOOTHPASTE, 40CT, 8.2OZ, UPC: 037000247081
D-0287-2026
Recall number D-0287-2026
Initiated December 26, 2025
Classification Class II
Status Ongoing
Quantity Unavailable
App-derived interpretation
Manufacturing or process control
reason.manufacturing_process_control · v1.0.0
CGMP Deviations
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Code information All lots within expiry distributed by Gold Star Distribution.
Distribution pattern US Nationwide.
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[357]
FDA event record
· Exact recall-number query on openFDA
