US Drug Recall Register
Class II · Moderate risk Terminated Initiated Aug 8, 2013 (13 years ago)

K EFFERVESCENT TABLETS, 25 meq POTASSIUM (977 mg), ORANGE FLAVORED, Potassium Bicarbonate…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

LABELING: Label Mix-up: 30 count Effervescent Potassium/Chloride Tablets, may be labeled as 30 count K Effervescent Tablets.

What was recalled

K EFFERVESCENT TABLETS, 25 meq POTASSIUM (977 mg), ORANGE FLAVORED, Potassium Bicarbonate Effervescent Tablets For Oral Solution, Rx only, 30 count, Manufactured for: Qualitest Pharmaceuticals, Inc., Huntsville, AL 35811, Manufactured by: Tower Laboratories Ltd., Centerbrook, CT 06409

Recalling firm
Qualitest Pharmaceuticals
Origin
AL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1036-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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