Pfizer Inc. recalls Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Mf
Recalled March 21, 2018 · FDA recall D-0596-2018 · Pfizer
Hazard
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked. · FDA Class I
Units
53600 vials
Sold at
Nationwide in the USA
Description
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Product
Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618. NDC: 0703-0110-01
Manufacturer(s)
Pfizer Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →