Class I
Terminated
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
- Company
- Pfizer Inc.
- Recall Initiated
- February 7, 2018
- Posted
- March 21, 2018
- Recall Number
- D-0596-2018
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 53600 vials
- Firm Location
- New York, NY, United States
Reason for Recall
Non-Sterility: Confirmed customer complaints of glass product container vials that may be empty or cracked.
Distribution
Nationwide in the USA
Lot / Code Info
Lots # 691853F, EXP. 9/1/2018; 700753F, EXP. 10/1/2018.
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