FDAClass IISeptember 18, 2013

Effervescent Potassium/chloride Tablets recall: Labeling Error

EFFERVESCENT POTASSIUM/CHLORIDE TABLETS, 25 meq Potassium Chloride (1865 mg), POTASSIUM BICARBONATE AND POTASSIUM CHLORIDE EFFERVESCENT TABLETS FOR…

Why was Effervescent Potassium/chloride Tablets recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot Number 21230-2, Exp. DEC 2015

Product
EFFERVESCENT POTASSIUM/CHLORIDE TABLETS, 25 meq Potassium Chloride (1865 mg), POTASSIUM BICARBONATE AND POTASSIUM CHLORIDE EFFERVESCENT TABLETS FOR…
Recalling firm
Qualitest Pharmaceuticals
Quantity
1680 boxes
Distribution
Natiowide
Recall date
September 18, 2013
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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