Autoject EI recall
Autoject EI, REF AJ1310
Why was Autoject EI 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
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot/Unit Number: V14
- Product
- Autoject EI, REF AJ1310
- Recalling firm
- Owen Mumford USA, Inc.
- Quantity
- 1510 units
- Distribution
- FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA
- Recall date
- November 13, 2019
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)