Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Potassium Chloride Recalled by Cardinal Health Due to Labeling: Incorrect or Missing Package Insert: the package...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cardinal Health directly.
Affected Products
Potassium Chloride, microencapsulated extended-release tablets, 20 mEq, blister card of 30/10 cards in a corrugated shipper, Rx only, Manufactured by Upsher-Smith Laboratories, Inc. Minneapolis, MN 55447 for Sandoz, Inc., Princeton, NJ 08540 Repackaged by Cardinal Health Zanesville, OH 43701
Quantity: 100 blister cards
Why Was This 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.
Where Was This Sold?
This product was distributed to 1 state: OK
About Cardinal Health
Cardinal Health has 75 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report