IV Start Kit — Class II medical device recall Z-1394-2024
Ongoing recall by Medical Action Industries, Inc. 306, reported 2024-04-03, distributed nationwide. The kits contain saline flush syringes which were recalled by the supplier.
| Recall number | Z-1394-2024 |
|---|---|
| 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 | 2024-01-15 |
| Classified | 2024-03-28 |
| Reported by FDA | 2024-04-03 |
| Distributed | Nationwide (US) |
| Quantity | 206,200 kits |
| UPC / GTIN / UDI-DI | 10809160020388 |
| Lot numbers | 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311741, 312807, 313961 |
| Model numbers | 100, 74654 |
Product
IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Reason for recall
The kits contain saline flush syringes which were recalled by the supplier.
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-1394-2024. 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.