Owen Mumford USA, Inc. Petfine Auto Injector, REF 3310VET Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Petfine Auto Injector, REF 3310VET
Brand
Owen Mumford USA, Inc.
Lot Codes / Batch Numbers
batches V14.V976 and V14.W107
Products Sold
batches V14.V976 and V14.W107
Owen Mumford USA, Inc. is recalling Petfine Auto Injector, REF 3310VET due to 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 (bra. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
The firm initiated the recall by letter on 07/17/2019. The consignee was directed to quarantine all affected product and contact the company for return. Distributors were also directed to cease distribution and contact their customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
CA, CO, FL, KY, LA, MO, NH, NJ, NY, NC, PA, SC, TX
Page updated: Jan 10, 2026