RecallRadar

FDA Drug recall D-0141-2026

Everolimus tablets 10 mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceuti…

On 2025-11-05 the FDA classified a Class III recall of Everolimus tablets 10 mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceuti… by Endo Usa, citing failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0141-2026
ClassificationClass III
Statusongoing
Initiated2025-10-10
Published2025-11-05
Last updated2026-09-13 11:52 UTC
CompanyEndo Usa
DistributionUS

Product

Everolimus tablets 10 mg, 28 tablets (each carton contains 4 blister strips with 7 tablets each), Rx only, Manufactured by: Par Pharmaceutical Chestnut Ridge, NY 10977 NDC# 49884-128-91

Reason

Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.

Identifiers

code_infoLot #: 550162801, Exp. Date NOV-25; 550169801, Exp. Date JAN-26

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-0141-2026%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.