Drug Depot, Inc., dba APS Pharmacy recalls (CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy
- Recall date
- March 23, 2022
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0729-2022
- FDA classification
- Class II
- Brand / firm
- Drug Depot, Inc., dba APS Pharmacy
- Sold / distributed
- Nationwide in the USA including Puerto Rico.
Why it was recalled
Lack of sterility assurance.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy
Get recall alerts
Free email alert whenever Drug Depot, Inc., dba APS Pharmacy has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Drug Depot, Inc., dba APS Pharmacy