Cantrell Drug Company recalls HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Can
Recalled December 21, 2016 · FDA recall D-0195-2017 · Cantrell Drug
Hazard
Lack of Assurance of Sterility - the firm is recalling select sterile drug products. · FDA Class II
Units
935 syringes
Sold at
Nationwide
Description
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Product
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
Manufacturer(s)
Cantrell Drug Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →