PlainRecalls
FDA Drug Moderate Class II Terminated

HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04

Reported: December 21, 2016 Initiated: November 18, 2016 #D-0195-2017

Product Description

HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04

Reason for Recall

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Details

Recalling Firm
Cantrell Drug Company
Units Affected
935 syringes
Distribution
Nationwide
Location
Little Rock, AR

Frequently Asked Questions

What product was recalled?
HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-04. Recalled by Cantrell Drug Company. Units affected: 935 syringes.
Why was this product recalled?
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Which agency issued this recall?
This recall was issued by the FDA Drug on December 21, 2016. Severity: Moderate. Recall number: D-0195-2017.