Is Autoject EI, REF AJ1310 recalled?

Medium RiskFDA Device

Owen Mumford USA, Inc.: 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

Agency Publication Date: November 1, 2019

Affected Products

Product: Autoject EI, REF AJ1310

Lot/Unit Number: V14

Product: Petfine Auto Injector, REF 3310VET

batches V14.V976 and V14.W107

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 83465

Status: Active

Manufacturer: Owen Mumford USA, Inc.

Manufactured In: United States

Units Affected: 2 products (1510 units; 140 units)

Were You Affected by This Recall?

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

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