Advanced Pharma Inc. recalls HYDROmorphone HCl 1 mg in 0.9% Sodium Chloride, QS 5 mL Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single us
Recalled March 27, 2019 · FDA recall D-1016-2019 · Advanced Pharma
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
2400 syringes
Sold at
Nationwide
Description
Lack of Assurance of Sterility
Product
HYDROmorphone HCl 1 mg in 0.9% Sodium Chloride, QS 5 mL Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe, NDC: 42852-289-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
Manufacturer(s)
Advanced Pharma Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →