US Drug Recall Register
Class III · Low risk Terminated Initiated Mar 10, 2022 (4 years ago)

Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for…

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

Why it was recalled

FAILED CONTENT UNIFORMITY SPECIFICATIONS

What was recalled

Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for: Macleods Pharma USA, Plainsboro, NJ 08536, Manufactured by: Macleods Pharmaceuticals Ltd., BAddi, HImchal Pradesh, INDIA, NDC 33342-107-07.

Recalling firm
Macleods Pharma Usa Inc
NDC code
33342-107-07
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0762-2022

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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