US Drug Recall Register
Class III · Low risk Terminated Initiated Feb 17, 2020 (7 years ago)

Potassium Chloride Extended-Release Tablets USP, 10mEq (750mg), 1000-count bottle, Rx…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Tablet/Capsules Specifications: Oversized tablets were found in one lot of Potassium Chloride Tablets 750 mg.

What was recalled

Potassium Chloride Extended-Release Tablets USP, 10mEq (750mg), 1000-count bottle, Rx only, Manufactured by: Strides Shasun Limited Bengaluru - 562106, India, Distributed by: Strides Pharma Inc., East Brunswick, NJ 08816, NDC 64380-861-08

Recalling firm
Strides Pharma Science Limited
NDC code
64380-861-08
Origin
India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1029-2020

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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