FDA Drug Recalls

Recalls / Class II

Class IID-1160-2017

Product

Bevacizumab Prefilled 30g and 31 gram 1.25mg/0.05mL Syringes, Rx only, Bella Pharma 3101 W. Devon Ave., Chicago, IL 60659, 1 (877) BELLA.

Affected lot / code info
Lot #: 3141201, Exp. 9/13/17; 3146966, Exp . 9/20/17; 3160608, Exp. 10/5/17; 3146966, Exp. 11/1/17

Why it was recalled

Lack of Assurance of Sterility.

Recalling firm

Firm
Bella Pharmaceuticals, Inc.
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
3101 W Devon Ave, N/A, Chicago, Illinois 60659-1407

Distribution

Quantity
2,334 syringes
Distribution pattern
Nationwide within USA

Timeline

Recall initiated
2017-08-15
FDA classified
2017-09-12
Posted by FDA
2017-09-20
Terminated
2018-04-23
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1160-2017. 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