RecallRadar

FDA Drug recall D-0136-2017

Clonazepam Tablets, USP, 1.0 mg, packaged in a 100- count unit dose box of 10 x 10 blister cards, Rx only, Manufactured by Mylan Pharmaceut…

On 2016-11-16 the FDA classified a Class III recall of Clonazepam Tablets, USP, 1.0 mg, packaged in a 100- count unit dose box of 10 x 10 blister cards, Rx only, Manufactured by Mylan Pharmaceut… by Mylan Institutional D B A Udl Laboratories, citing failed Impurities/Degradation Specifications: out of specification result for Clonazepam Related Compound (RC) A (a known impurity) at 16 month timepoint.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0136-2017
ClassificationClass III
Statusterminated
Initiated2016-09-28
Published2016-11-16
Last updated2026-09-13 11:51 UTC
CompanyMylan Institutional D B A Udl Laboratories
DistributionUS

Product

Clonazepam Tablets, USP, 1.0 mg, packaged in a 100- count unit dose box of 10 x 10 blister cards, Rx only, Manufactured by Mylan Pharmaceuticals Inc, Morgantown, WV, 26505, NDC 51079-882-20

Reason

Failed Impurities/Degradation Specifications: out of specification result for Clonazepam Related Compound (RC) A (a known impurity) at 16 month timepoint.

Identifiers

code_infoLot#: 3061784, Exp 11/16; 3067656, Exp 12/16; 3074902, Exp 08/17

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-0136-2017%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.