Reported Nov 13, 2019 · Ongoing
Autoject EI, REF AJ1310
Owen Mumford USA, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Owen Mumford USA, Inc. · 1755 W Oak Commons Ct · Marietta, GA · 30062-2280
Is this the product you have?
- Autoject EI, REF AJ1310
- Lot codes and dates
- Lot/Unit NumberV14
- Amount recalled
- 1510 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1310, lot number V14 and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 & V14.W107
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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