FDA Drug Recalls

Recalls / Class II

Class IID-0641-2016

Product

GENTAMICIN, Packaged as a) 70MG in 70ML Homepumps, b) 80MG in 80ML Homepumps, and c) 375MG in a 75ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.

Affected lot / code info
All Lots compounded between 11-Sep-15 and 17-Sep-15. Expiries: a) 30-Sep-15, b) 25-Sep-15, c) 24-Sep-15

Why it was recalled

Lack of Assurance of Sterility: Product sterility cannot be guaranteed.

Recalling firm

Firm
Sentara Enterprises
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
535 Independence Pkwy Ste 300, N/A, Chesapeake, Virginia 23320-5176

Distribution

Quantity
a) 11 bags, b) 9 Bags, c) 3 Bags
Distribution pattern
U.S. Including: VA, NC

Timeline

Recall initiated
2015-09-18
FDA classified
2016-01-28
Posted by FDA
2016-02-03
Terminated
2016-06-29
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0641-2016. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.