Recall events
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Event 89512
Event summary
Timeline bucket October 06, 2021
Product types Food
Classifications Class II
Statuses Terminated
Recalling firm wording ULTRAtab Laboratories, Inc.
Dossier provenance
Source snapshots represented here
openFDA Food 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
9 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.
food · product 1 of 9
Ephrine Plus Tablet (Caffeine 200 mg, Vitamin C 25 mg) Supplement, ULTRAtab Laboratories, Inc., Highland, NY
F-0721-2022
Recall number F-0721-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 4,250,842 tablets
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
Code information Product Codes: M943 M943L Bulk Lots: 16K038, 18B075
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28936]
FDA event record
· Exact recall-number query on openFDA
food · product 2 of 9
Electrolyte tablet (Calcium 10.8mg, Potassium 40mg, Magnesium 12 mg), ULTRAtab Laboratories, Inc., Highland, NY
F-0722-2022
Recall number F-0722-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 26,682,419 tablets
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
Code information Product Codes: M693 Bulk Lots: 18J001, 18J002, 18J003, 18L035, 18L036, 18M013, 18M014, 19A044, 19A045, 19B042, 19B043, 19B066, 19C006, 19C007, 19E065, 19E066, 19J045, 19J046
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28555]
FDA event record
· Exact recall-number query on openFDA
food · product 3 of 9
Caffeine 125 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY
F-0723-2022
Recall number F-0723-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 1,904,760 tablets
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
Code information Product Codes: M960L Bulk Lots: 19E021, 19E022
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28719]
FDA event record
· Exact recall-number query on openFDA
food · product 4 of 9
Caffeine 150 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY
F-0724-2022
Recall number F-0724-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 1,606,966 tablets
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
Code information Product Codes: M961L Bulk Lots: 19E030, 19E031
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28793]
FDA event record
· Exact recall-number query on openFDA
food · product 5 of 9
Caffeine 175 mg with B6 and B12 vitamins (supplement), ULTRAtab Laboratories, Inc., Highland, NY
F-0725-2022
Recall number F-0725-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 1,393,353 tablets
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
Code information Product Codes: M962L Bulk Lots: 19E032, 19E033
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28724]
FDA event record
· Exact recall-number query on openFDA
food · product 6 of 9
Melatonin ER 0.5 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY
F-0726-2022
Recall number F-0726-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 955,928 tablets
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
Code information Product Codes: M975 Bulk Lots: 19E058
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28425]
FDA event record
· Exact recall-number query on openFDA
food · product 7 of 9
Melatonin ER 2 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY
F-0727-2022
Recall number F-0727-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 5,853,539 tablets
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
Code information Product Codes: M976 Bulk Lots: 19B050, 19F063
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[27953]
FDA event record
· Exact recall-number query on openFDA
food · product 8 of 9
Melatonin ER 5 mg caplet (supplement), ULTRAtab Laboratories, Inc., Highland, NY
F-0728-2022
Recall number F-0728-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 1,478,344 tablets
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
Code information Product Codes: M977A Bulk Lots: 19B011, 19B012, 19E023
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28852]
FDA event record
· Exact recall-number query on openFDA
food · product 9 of 9
MidNite Tablet (Melatonin 1.5 mg) supplement, ULTRAtab Laboratories, Inc., Highland, NY
F-0729-2022
Recall number F-0729-2022
Initiated October 06, 2021
Classification Class II
Status Terminated
Quantity 42,352,387 tablets
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
Code information Product Codes: M978 Bulk Lots: 18J069, 18J070, 18J071, 18M072, 18L124, 18L125, 18L126, 19C037, 19C038, 19C039, 19C040,19D029, 19D030, 19D031, 19G047, 19G048, 19G049, 19G050
Distribution pattern Bulk product was distributed to 2 distributors (NY, FL) who may have repackaged the product and further distributed finished product.
Official fact provenance
Dataset openFDA Food Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 ccbd901395e7f97453ba67323214b452ee901a828cb9048da8cb62e875bf39dc
Raw source locator 0001-food-enforcement-0001-of-0001.json.zip#results[28561]
FDA event record
· Exact recall-number query on openFDA
