Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Distributed by: Belmora LLC, PO Box 3063, Arlington, VA 22203, UPC 8 53030 00209 0, NDC 27854.101.01.
Reported: January 30, 2013 Initiated: December 18, 2012 #D-136-2013
Product Description
Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Distributed by: Belmora LLC, PO Box 3063, Arlington, VA 22203, UPC 8 53030 00209 0, NDC 27854.101.01.
Reason for Recall
Defective Container: Product lacks tamper evident breakaway band on cap.
Details
- Recalling Firm
- Belmora LLC
- Units Affected
- 17,996 bottles
- Distribution
- Nationwide
- Location
- Arlington, VA
Frequently Asked Questions
What product was recalled? ▼
Flanax (aluminum hydroxide, magnesium hydroxide, and simethicone) Fast Acting Antacid, 200 mg/200 mg/20 mg, 12 fl oz (355 mL) bottles, Distributed by: Belmora LLC, PO Box 3063, Arlington, VA 22203, UPC 8 53030 00209 0, NDC 27854.101.01.. Recalled by Belmora LLC. Units affected: 17,996 bottles.
Why was this product recalled? ▼
Defective Container: Product lacks tamper evident breakaway band on cap.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 30, 2013. Severity: Low. Recall number: D-136-2013.
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