Advanced Pharma Inc. recalls HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use
Recalled May 8, 2019 · FDA recall D-1251-2019 · Advanced Pharma
Hazard
Sub-potency · FDA Class II
Units
560 bags
Sold at
Nationwide in the US
Description
Sub-potency
Product
HYDROmorphone 20 mg/100 mL Injectable Solution, Hydromorphone HCl 20 mg 0.9% Sodium Chloride 100 mL, Sterile single use bag, Compounded Drug, Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404, NDC: 42852-221-10
Manufacturer(s)
Advanced Pharma Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →