Recall events
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Event 77484
Event summary
Timeline bucket March 30, 2017
Product types Drug
Classifications Class II
Statuses Terminated
Recalling firm wording Bayer HealthCare Pharmaceuticals, 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
3 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 3
Alka-Seltzer Original ( 325 mg Aspirin (NSAID), 1916 mg Analgesic, Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 12-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500040194
D-1044-2017
Recall number D-1044-2017
Initiated March 30, 2017
Classification Class II
Status Terminated
Quantity 1,067,520 12-count cartons
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Code information BTAH340; Exp. 02/19 BTAHCP0; Exp. 04/19 BTAHLW0; Exp. 06/19 BTAHLX0; Exp. 08/19 BTAHP10; Exp 08/19
Distribution pattern 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[9824]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 3
Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 24-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500044048
D-1050-2017
Recall number D-1050-2017
Initiated March 30, 2017
Classification Class II
Status Terminated
Quantity 24,672 24-count cartons
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Code information BTAHDG0; Exp. 04/19
Distribution pattern 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[9470]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 3
Alka-Seltzer Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbonate/Antacid) Effervescent Tablets, 36-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500041085
D-1051-2017
Recall number D-1051-2017
Initiated March 30, 2017
Classification Class II
Status Terminated
Quantity 56,064 36-count cartons
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
These labels are deterministic app interpretations, not FDA categories.
Inspect official wording and provenance
Reason for recall Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Code information BTAHGR0; Exp. 05/19 BTAHGR1; Exp. 05/19 BTAHGR2; Exp. 05/19 BTAJ0K3; Exp. 07/19
Distribution pattern 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[7555]
FDA event record
· Exact recall-number query on openFDA