Advanced Pharma Inc. recalls fentaNYL 2500 mcg/250 mL Injectable Solution, Fentanyl 0.9% Sodium Chloride, QS, Sterile single use bags, NDC: 42852-210
Recalled March 27, 2019 · FDA recall D-1018-2019 · Advanced Pharma
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
180 bags
Sold at
Nationwide
Description
Lack of Assurance of Sterility
Product
fentaNYL 2500 mcg/250 mL Injectable Solution, Fentanyl 0.9% Sodium Chloride, QS, Sterile single use bags, NDC: 42852-210-25 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 →