Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Autoject E1 Fixed needle device Recalled by Owen Mumford USA, Inc. Due to The syringe carrier is missing components: a damper...
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 Owen Mumford USA, Inc. directly.
Affected Products
Autoject E1 Fixed needle device, Model Number AJ1310, UPC Code 384701310010 The Autoject E1 is an injector used by patients to inject drugs as prescribed by their doctor.
Quantity: 3,100
Why Was This Recalled?
The syringe carrier is missing components: a damper and spring.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Owen Mumford USA, Inc.
Owen Mumford USA, Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report