RecallRadar

FDA Drug recall D-0727-2018

Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited…

On 2018-05-16 the FDA classified a Class II recall of Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited… by Dr Reddy S Laboratories, citing presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0727-2018
ClassificationClass II
Statusterminated
Initiated2018-04-23
Published2018-05-16
Last updated2026-09-13 11:52 UTC
CompanyDr Reddy S Laboratories
DistributionUS

Product

Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100 Tablets bottle, Rx only, Manufactured by: Dr. Reddy's Laboratories Limited Bachupally-500 090 India\ NDC 55111-468-01

Reason

Presence of Foreign Tablets/Capsules: One foreign tablet identified as Clopidogrel 75 mg was found in a 100 count bottle of Metoprolol Succiante Extended-Release Tablets.

Identifiers

ndc55111-468-30
ndc55111-468-60
ndc55111-468-01
ndc55111-468-05
ndc55111-468-79
ndc55111-468-78
ndc55111-469-30
ndc55111-469-60
ndc55111-469-01
ndc55111-469-05
ndc55111-469-79
ndc55111-469-78
code_infoBatch # C706254, 08/2019

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-0727-2018%22

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