PlainRecalls
FDA Drug Moderate Class II Terminated

(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy

Reported: April 6, 2022 Initiated: March 23, 2022 #D-0729-2022

Product Description

(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy

Reason for Recall

Lack of sterility assurance.

Details

Units Affected
1843 vials
Distribution
Nationwide in the USA including Puerto Rico.
Location
Palm Harbor, FL

Frequently Asked Questions

What product was recalled?
(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy. Recalled by Drug Depot, Inc., dba APS Pharmacy. Units affected: 1843 vials.
Why was this product recalled?
Lack of sterility assurance.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 6, 2022. Severity: Moderate. Recall number: D-0729-2022.