RecallRadar

FDA Drug recall D-0762-2022

Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for: Macleods Pharma USA, Plainsboro, NJ 08536, Manufactured…

On 2022-04-13 the FDA classified a Class III recall of Risedronate Sodium Tablets, USP, 5 mg, Rx Only, 30-count bottle, Manufactured for: Macleods Pharma USA, Plainsboro, NJ 08536, Manufactured… by Macleods Pharma Usa, citing FAILED CONTENT UNIFORMITY SPECIFICATIONS.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0762-2022
ClassificationClass III
Statusterminated
Initiated2022-03-10
Published2022-04-13
Last updated2026-09-13 11:52 UTC
CompanyMacleods Pharma Usa
DistributionUS

Product

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.

Reason

FAILED CONTENT UNIFORMITY SPECIFICATIONS

Identifiers

ndc33342-107-07
ndc33342-107-49
ndc33342-107-06
ndc33342-108-07
ndc33342-108-15
ndc33342-108-06
ndc33342-109-37
ndc33342-109-50
code_infoLot #: BRD2001A, Exp 5/2022

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0762-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.