RecallRadar

FDA Drug recall D-0357-2026

Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963…

On 2026-03-11 the FDA classified a Class II recall of Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963… by Teva Pharmaceuticals Usa, citing failed Dissolution Specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0357-2026
ClassificationClass II
Statusongoing
Initiated2026-01-29
Published2026-03-11
Last updated2026-09-13 11:52 UTC
CompanyTeva Pharmaceuticals Usa
DistributionUS

Product

Metoprolol Succinate Extended-Release Tablets, 200 mg, 100 tablets bottles, Rx Only, Teva Pharmaceuticals, Parsippany, NJ 07054, NDC: 45963-678-11

Reason

Failed Dissolution Specifications

Identifiers

ndc45963-709-11
ndc45963-709-96
ndc45963-676-11
ndc45963-676-96
ndc45963-677-11
ndc45963-677-96
ndc45963-678-11
code_infoLot#: a) 0686H251, 0687H251, 10688H251, Exp.: 02/2027. .

Status history

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

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0357-2026%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.