FDA Drug Recalls

Recalls / Class II

Class IID-1201-2022

Product

Estradiol Cypionate 10mg/mL, a) 1mL-vial, b) 2 mL-vial, Room Temperature, Tailor Made Compounding

Affected lot / code info
Batch #: a) 01052210A1, Exp 4/5/2022; 10202101A1, Exp 4/18/2022; 01052210A1 7/4/2022; b)10202102A1, Exp 4/18/2022; 12022126A1, Exp 5/31/2022; 01052210A1, Exp 7/4/2022.

Why it was recalled

Lack of Assurance of Sterility

Recalling firm

Firm
TMC Acquisition LLC dba Tailor Made Compounding
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
200 Moore Dr, Nicholasville, Kentucky 40356-8512

Distribution

Quantity
349 vials
Distribution pattern
Nationwide USA and Puerto Rico

Timeline

Recall initiated
2022-03-07
FDA classified
2022-07-14
Posted by FDA
2022-07-20
Status
Ongoing

Source: openFDA Drug Enforcement endpoint. Recall record D-1201-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls