Owen Mumford Recalls Petfine Auto Injectors Due to Assembly Error
Owen Mumford USA is recalling 140 Petfine Auto Injectors due to a possible assembly error in the Autoject EI component.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text describes a 'possible assembly error' without reporting any injuries, illnesses, or specific functional failures, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Owen Mumford USA, Inc. is recalling 140 units of the Petfine Auto Injector, REF 3310VET, due to a possible assembly error. The error is associated with the Autoject EI component, lot number V14.
The affected Autoject EI lot was packed into two products: AJ 1310, lot number V14, and AN 3310VET (branded as Petfine Auto Injector), batches V14.V976 and V14.W107. The recalled units were distributed in Florida, Louisiana, South Carolina, California, New Jersey, Texas, North Carolina, Colorado, New Hampshire, Kentucky, New York, Missouri, and Pennsylvania.
Consumers should check their inventory for the specific lot and batch numbers listed above. If the product matches the recalled description, they should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Petfine Auto Injector, REF 3310VET
- Manufacturer
- Owen Mumford USA, Inc.
- Hazard
- Affected units
- 140
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- batches V14.V976 and V14.W107
Distribution
Part of a larger recall action
This product is one of 2 recalled by Owen Mumford USA, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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