Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Epinephrine Injection USP Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations: Precautions taken due to Out-of-specification for...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Teva Pharmaceuticals USA directly.
Affected Products
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
Quantity: 600 cartons/2 auto-injector per carton
Why Was This Recalled?
CGMP Deviations: Precautions taken due to Out-of-specification for trigger force for a non-marketed lot number that shares the same component.
Where Was This Sold?
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.
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report