FDAFDA · Food and drugs·Recall number D-0988-2022
Alprostadil Injection USP 500 mcg/mL, 1 mL Single Dose Vial, 5 vials per Carton, Rx Only, Carton NDC 0703-1501-02, Distributed by: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, Vial NDC 0703-1501-01
Published June 15, 2022 · Recall initiated: May 18, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications; out-of-specification results for impurities obtained during routine stability testing
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Teva Pharmaceuticals USA Inc
- Distributor
- Product was distributed nationwide in the US Market
- Lot
- Lot #:100022404, Exp Date 10/2022; Lot #:100023333, Exp Dat 12/2022
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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