Petfine Auto Injector — Class II medical device recall Z-0264-2020
Ongoing recall by Owen Mumford USA, Inc., reported 2019-11-13, distributed in CA, CO, FL, KY, LA, MO, NC, NH…. There is a possible assembly error on Autoject EI, lot number V14. This lot was packed into two products: AJ 1
| Recall number | Z-0264-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Owen Mumford USA, Inc., Marietta, GA, United States |
| Recall initiated | 2019-07-17 |
| Classified | 2019-11-01 |
| Reported by FDA | 2019-11-13 |
| Distributed | CA, CO, FL, KY, LA, MO, NC, NH, NJ, NY, PA, SC, TX |
| Quantity | 140 units |
| Lot numbers | V14.V976, V14.W107 |
| Model numbers | 3310VET |
Product
Petfine Auto Injector, REF 3310VET
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
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0264-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.