FDA Drug Recalls

Recalls / Class II

Class IID-0735-2020

Product

HCG 10,000U/1ML INJ in 4 mL vial Assurance Infusion (713) 533-8800

Affected lot / code info
Lots: 12162019@38 Exp. 01/16/2020; 11272019@32 Exp. 12/31/2019

Why it was recalled

Lack of sterility assurance.

Recalling firm

Firm
Assurance Infusion
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
2626 S Loop W Ste 555, Houston, Texas 77054-2652

Distribution

Quantity
2 vials
Distribution pattern
Nationwide within the United States

Timeline

Recall initiated
2019-12-20
FDA classified
2020-01-13
Posted by FDA
2020-01-22
Terminated
2021-10-27
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0735-2020. 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