Brand Name: Medical Action Industries Product Name: Dialysis Change… — Class II medical device recall Z-2858-2026
Ongoing recall by Medical Action Industries, Inc. 306, reported 2026-08-12, distributed nationwide. Convenience kits contain needle free access device that has an improper seal which may result in doming or tea
| Recall number | Z-2858-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medical Action Industries, Inc. 306, Arden, NC, United States |
| Recall initiated | 2026-05-21 |
| Classified | 2026-08-03 |
| Reported by FDA | 2026-08-12 |
| Distributed | Nationwide (US) |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 20809160242558 |
| Lot numbers | 318461, 319980, 320965, 322375, 325653, 327075, 328690, 330775, 331356, 336680 |
| Model numbers | 78791 |
Product
Brand Name: Medical Action Industries Product Name: Dialysis Change Tray Clear Sequence Model/Catalog Number: 78791
Reason for recall
Convenience kits contain needle free access device that has an improper seal which may result in doming or tearing of the silicone seal.
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-2858-2026. 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.