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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 83465

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 17, 2019
Product types
Device
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Owen Mumford USA, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 2

Autoject EI, REF AJ1310

Z-0263-2020
Recall number
Z-0263-2020
Initiated
July 17, 2019
Classification
Class II
Status
Ongoing
Recalling firm
Owen Mumford USA, Inc.
Quantity
1510 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
assembly error

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

Lot/Unit Number: V14

Distribution pattern

FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA

device · product 2 of 2

Petfine Auto Injector, REF 3310VET

Z-0264-2020
Recall number
Z-0264-2020
Initiated
July 17, 2019
Classification
Class II
Status
Ongoing
Recalling firm
Owen Mumford USA, Inc.
Quantity
140 units

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
assembly error

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Employee error

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

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

Code information

batches V14.V976 and V14.W107

Distribution pattern

FL, LA, SC, CA, NJ, TX, NC, CO, NH, KY, NY, MO, PA