FDA (Devices) recall action 83465
The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.
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
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
Owen Mumford USA is recalling 1,510 units of Autoject EI devices due to a possible assembly error. The lot was distributed to 13 states.
Owen Mumford USA is recalling 140 Petfine Auto Injectors due to a possible assembly error in the Autoject EI component.