Sentara Enterprises recalls HYDROMORPHONE HCL, Packaged as a) 2.5MG in 1ML Syringes, b) 150MG in 75ML Homepumps, c) 125MG in 125ML Homepumps, d) 250
Recalled February 3, 2016 · FDA recall D-0625-2016 · Sentara Enterprises
Hazard
Lack of Assurance of Sterility: Product sterility cannot be guaranteed. · FDA Class II
Units
a) 42 Syringes, b) 6 Bags, c) 4 Bags, d) 4 Bags, e) 1 Bag
Sold at
U.S. Including: VA, NC
Description
Lack of Assurance of Sterility: Product sterility cannot be guaranteed.
Product
HYDROMORPHONE HCL, Packaged as a) 2.5MG in 1ML Syringes, b) 150MG in 75ML Homepumps, c) 125MG in 125ML Homepumps, d) 250MG in 125ML Homepumps, e) 135MG in 135ML Homepumps, Rx Only. SENTARA HOME HEALTH SENTARA RX, 535 Independence Pkwy ste.300, Chesapeake, VA 23320-5176.
Manufacturer(s)
Sentara Enterprises
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →