Medical Action INDUSTRIES INC — Class II medical device recall Z-0751-2023
Terminated recall by Medical Action Industries, Inc. 306, reported 2022-12-28, distributed nationwide. XXX
| Recall number | Z-0751-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Action Industries, Inc. 306, Arden, NC, United States |
| Recall initiated | 2022-11-04 |
| Classified | 2022-12-21 |
| Reported by FDA | 2022-12-28 |
| Terminated | 2026-03-18 |
| Distributed | Nationwide (US) |
| Quantity | 198 cases |
| UPC / GTIN / UDI-DI | 10809160156681 |
| Lot numbers | 297223, 297418 |
| Model numbers | 58647D |
Product
Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit
Reason for recall
XXX
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-0751-2023. 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.