Cantrell Drug Company recalls Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial (1 mg/mL), Single-Dose Injection Solution For Slow IV U
Recalled December 21, 2016 · FDA recall D-0196-2017 · Cantrell Drug
Hazard
Lack of Assurance of Sterility - the firm is recalling select sterile drug products. · FDA Class II
Units
93 vials
Sold at
Nationwide
Description
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Product
Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride 30 mL PCA Vial (1 mg/mL), Single-Dose Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-006-10
Manufacturer(s)
Cantrell Drug Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →