FDA Drug Recalls

Recalls / Class II

Class IID-1271-2019

Product

BEVACIZUMAB 1.25 mg/0.05 mL 31G MJ syringe Intravitreal Injection. This biologic product was repackaged by AmEx Pharmacy 1515 Elizabeth St. Suite J Melbourne, FL 32901 Lot:190212AB BUD:5/13/2019, Repackaged on 2/12/2019

Affected lot / code info
Lot: 190212AB BUD: 5/13/2019

Why it was recalled

Defective Delivery System: difficult to express

Recalling firm

Firm
Pacifico National, Inc. dba AmEx Pharmacy
Notification channel
Telephone
Type
Voluntary: Firm initiated
Address
1515 Elizabeth St Ste J, N/A, Melbourne, Florida 32901-3000

Distribution

Quantity
249 syringes
Distribution pattern
Nationwide in the US

Timeline

Recall initiated
2019-04-19
FDA classified
2019-05-07
Posted by FDA
2019-05-08
Terminated
2021-02-16
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1271-2019. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.