Lincare, Inc. recalls HYDROmorphone HCl PF, Hydromorphone 1000 mg / NS 500 mL, Qty: 1 500 mL Bag, Rx Only. Compounded by: United Medical IV C
Recalled July 8, 2015 · FDA recall D-1202-2015 · Lincare
Hazard
Lack of Assurance of Sterility: Sterility of product is not assured. · FDA Class II
Units
1 Bag
Sold at
United States including: Arkansas
Description
Lack of Assurance of Sterility: Sterility of product is not assured.
Product
HYDROmorphone HCl PF, Hydromorphone 1000 mg / NS 500 mL, Qty: 1 500 mL Bag, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
Manufacturer(s)
Lincare, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →