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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 77484

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

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

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

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

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

Field note

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