Argon Medical Devices — Class II medical device recall Z-2239-2023
Ongoing recall by Argon Medical Devices, Inc, reported 2023-08-02, distributed nationwide. There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary emb
| Recall number | Z-2239-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Argon Medical Devices, Inc, Athens, TX, United States |
| Recall initiated | 2023-06-08 |
| Classified | 2023-07-27 |
| Reported by FDA | 2023-08-02 |
| Distributed | Nationwide (US) |
| Quantity | 3 |
| UPC / GTIN / UDI-DI | 00886333217151 |
| Lot numbers | 11481383 |
| Model numbers | 352506070E |
Product
Argon Medical Devices, REF 352506070E, Option Elite Retrievable Vena Cava Filter, Suitable of Jugular or Femoral Delivery, STERILEO, RxOnly, CE 2797
Reason for recall
There is the potential that the vena Cava Filter may not perform as intended which may result in pulmonary embolism.
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-2239-2023. 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.