RecallRadar

FDA Drug recall D-1176-2022

Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical Industries Inc., Cranbur…

On 2022-07-13 the FDA classified a Class II recall of Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical Industries Inc., Cranbur… by Sun Pharmaceutical Industries, citing CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1176-2022
ClassificationClass II
Statusterminated
Initiated2022-06-03
Published2022-07-13
Last updated2026-09-13 11:52 UTC
CompanySun Pharmaceutical Industries
DistributionUS

Product

Testosterone Cypionate Injection, USP, 200mg/ml, Rx Only, One Single-dose vial, Distributed by: Sun Pharmaceutical Industries Inc., Cranbury, NJ 08512, Manufactured by: Sun Pharmaceuticals Industries Ltd., Halol-Baroda Highway, Halol-389 350, Gujarat, India, NDC 62756-015-40.

Reason

CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.

Identifiers

ndc62756-017-40
ndc62756-015-40
ndc62756-016-40
code_infoLots JKX3267A & JKX3686A Exp. Date 08/2022 Lot JKX4700A, Exp Date 10/2022 Lot JKX5727A, Exp date 11/2022

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-1176-2022%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.