Medical Action Industries Inc — Class I medical device recall Z-2007-2026
Ongoing recall by Medical Action Industries, Inc. 306, reported 2026-05-13, distributed in AZ. Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose c
| Recall number | Z-2007-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Action Industries, Inc. 306, Arden, NC, United States |
| Recall initiated | 2026-03-17 |
| Classified | 2026-05-06 |
| Reported by FDA | 2026-05-13 |
| Distributed | AZ |
| Quantity | 2,030 kits |
| UPC / GTIN / UDI-DI | 20809160490294 |
| Lot numbers | 335489, 336189, 336789, 337365, 338434, 339423, 342509, 346066 |
| Model numbers | BHCA49K |
Product
Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
Reason for recall
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
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-2007-2026. 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.