FDA Device recall Z-0264-2020
Petfine Auto Injector, REF 3310VET
- FDA Device
- Class II
- ongoing
- Published 2019-11-13
On 2019-11-13 the FDA classified a Class II recall of Petfine Auto Injector, REF 3310VET by Owen Mumford Usa, citing 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)….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0264-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2019-07-17 |
| Published | 2019-11-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Owen Mumford Usa |
| Distribution | CA, CO, FL, KY, LA, MO, NC, NH, NJ, NY, PA, SC, TX |
Product
Petfine Auto Injector, REF 3310VET
Reason
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
Identifiers
| code_info | batches V14.V976 and V14.W107 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0264-2020%22
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