Potassium Chloride recall: Labeling Error
Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated shipper, Rx only, Manufactured by…
Why was Potassium Chloride recalled?
Labeling: Incorrect or Missing Package Insert: the package insert for the potassium chloride 8 mEq and 10 mEq strength instead of the potassium chloride 10 mEq and 20 mEq strength was packaged with the product.
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 #: 315004A, Exp 1/15/14; Lot #: 315620A, Exp 1/15/14
- Product
- Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated shipper, Rx only, Manufactured by…
- Recalling firm
- Cardinal Health
- Quantity
- 100 blister cards
- Distribution
- OK
- Recall date
- April 22, 2015
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)