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
Reported: January 21, 2026 Initiated: December 26, 2025 #D-0263-2026
Product Description
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
Reason for Recall
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Details
- Recalling Firm
- GOLD STAR DISTRIBUTION INC
- Units Affected
- Unknown
- Distribution
- US Nationwide.
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by GOLD STAR DISTRIBUTION INC. Units affected: Unknown.
Why was this product recalled? ▼
CGMP Deviations: Insanitary conditions including rodent exposure/activity in their distribution center.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 21, 2026. Severity: Moderate. Recall number: D-0263-2026.
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