FDA Drug Recalls

Recalls / Class I

Class ID-0869-2016

Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.

Product

Avastin (Bevacizumab) 2 mg/0.08 mL syringe, Office Administration Only, AmEx Pharmacy, 1515 Elizabeth St Suite J, Melbourne, FL 32901.

Affected lot / code info
Lot #: 141224C, Exp. 03/24/2015; 150915B, Exp. 12/14/2015

Why it was recalled

Non-Sterility: Product tested positive for bacterial contamination.

Recalling firm

Firm
Pacifico National, Inc. dba AmEx Pharmacy
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
1515 Elizabeth St Ste J, N/A, Melbourne, Florida 32901-3000

Distribution

Quantity
45 syringes
Distribution pattern
Nationwide

Timeline

Recall initiated
2015-01-20
FDA classified
2016-05-25
Posted by FDA
2016-06-01
Terminated
2017-03-09
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0869-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.