FDA Device recall Z-1394-2024
IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile
- FDA Device
- Class II
- ongoing
- Published 2024-04-03
On 2024-04-03 the FDA classified a Class II recall of IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile by Medical Action Industries 306, citing the kits contain saline flush syringes which were recalled by the supplier.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1394-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-01-15 |
| Published | 2024-04-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medical Action Industries 306 |
| Distribution | US |
Product
IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.
Reason
The kits contain saline flush syringes which were recalled by the supplier.
Identifiers
| code_info | Lot numbers 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311…Lot numbers 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311741, 312807, and 313961;UDI-DI 10809160020388. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1394-2024%22
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