FDAFDA · Food and drugs·Recall number D-1260-2020
Epinephrine Injection USP, 0.3 mg (Auto-Injector), 0.3 mg/ 0.3 mL pre-filled syringe, Rx Only, Manufactured for Teva Pharmaceuticals USA, Inc. North Wales, PA 19454. NDC 0093-5986-27
Published May 13, 2020 · Recall initiated: March 5, 2020
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
CGMP Deviations: Precautions taken due to Out-of-specification for trigger force for a non-marketed lot number that shares the same component.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- EPINEPHRINE
- Manufacturer
- Teva Pharmaceuticals USA
- Distributor
- Product was distributed to 1 wholesaler who still had all units within their possession and had not shipped or further distributed any of the product.
- UPC
- 0300935985275
- Lot
- Lot # 007F19AA, exp. date 04/2021
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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