PlainRecalls
FDA Drug Moderate Class II Terminated

morphine sulfate 1 mg per mL in 0.9% Sodium Chloride, (Total morphine Dose 100 mg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, (877) 550-5059; labeled as a) NDC: 70004-0100-59; b) NDC: 70004-100-58.

Reported: August 2, 2017 Initiated: July 14, 2017 #D-0999-2017

Product Description

morphine sulfate 1 mg per mL in 0.9% Sodium Chloride, (Total morphine Dose 100 mg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, (877) 550-5059; labeled as a) NDC: 70004-0100-59; b) NDC: 70004-100-58.

Reason for Recall

Lack of Assurance of Sterility: Product made with recalled 0.9% sodium chloride bags which have the potential to leak.

Details

Recalling Firm
SCA Pharmaceuticals
Units Affected
220 bags
Distribution
Nationwide in the USA
Location
Little Rock, AR

Frequently Asked Questions

What product was recalled?
morphine sulfate 1 mg per mL in 0.9% Sodium Chloride, (Total morphine Dose 100 mg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, (877) 550-5059; labeled as a) NDC: 70004-0100-59; b) NDC: 70004-100-58.. Recalled by SCA Pharmaceuticals. Units affected: 220 bags.
Why was this product recalled?
Lack of Assurance of Sterility: Product made with recalled 0.9% sodium chloride bags which have the potential to leak.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 2, 2017. Severity: Moderate. Recall number: D-0999-2017.