Class II · Moderate risk Terminated
(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy
Reason Lack of sterility assurance.
Gonadorelin 100mcg/mL, 10mL per vial, Refrigerate, Tailor Made Compounding
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Assurance of Sterility
What was recalled
Gonadorelin 100mcg/mL, 10mL per vial, Refrigerate, Tailor Made Compounding
- Recalling firm
- TMC Acquisition LLC dba Tailor Made Compounding
- Origin
- KY, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-1207-2022
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Gonadorelin recalls
See all
Class II · Moderate risk Terminated
GONADORELIN (5ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID132227, APS Pharmacy
Reason Lack of sterility assurance.
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