PlainRecalls
FDA Drug Moderate Class II Terminated

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.

Reported: July 8, 2015 Initiated: May 28, 2015 #D-1202-2015

Product Description

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.

Reason for Recall

Lack of Assurance of Sterility: Sterility of product is not assured.

Details

Recalling Firm
Lincare, Inc.
Units Affected
1 Bag
Distribution
United States including: Arkansas
Location
Little Rock, AR

Frequently Asked Questions

What product was recalled?
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.. Recalled by Lincare, Inc.. Units affected: 1 Bag.
Why was this product recalled?
Lack of Assurance of Sterility: Sterility of product is not assured.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 8, 2015. Severity: Moderate. Recall number: D-1202-2015.