PlainRecalls
FDA Drug Low Class III Terminated

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.