RecallRadar

FDA Drug recall D-1080-2014

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd

On 2014-02-12 the FDA classified a Class II recall of Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd by Dr Reddy S Laboratories, citing failed Dissolution Specification; 12-Month stability interval.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1080-2014
ClassificationClass II
Statusterminated
Initiated2013-12-13
Published2014-02-12
Last updated2026-09-13 11:51 UTC
CompanyDr Reddy S Laboratories
DistributionLA, MI, MO, MS, OH

Product

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's Laboratories Limited Bachepalli -500 090 INDIA NDC 55111-467-01

Reason

Failed Dissolution Specification; 12-Month stability interval.

Identifiers

ndc55111-466-30
ndc55111-466-60
ndc55111-466-01
ndc55111-466-05
ndc55111-466-79
ndc55111-466-78
ndc55111-467-30
ndc55111-467-60
ndc55111-467-01
ndc55111-467-05
ndc55111-467-79
ndc55111-467-78
code_infoLot # C207420 and C207416

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1080-2014%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.