FDA Device recall Z-0650-2018
Multi Lumen Central Venous Catheterization Kit
- FDA Device
- Class II
- terminated
- Published 2018-02-28
On 2018-02-28 the FDA classified a Class II recall of Multi Lumen Central Venous Catheterization Kit by Arrow International, citing these finished good kits may contain the incorrect Springwire Guide (SWG).
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0650-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-10-17 |
| Published | 2018-02-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Arrow International |
| Distribution | US |
Product
Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2; Exp. Dates Feb 2018 - Nov 2018
Reason
These finished good kits may contain the incorrect Springwire Guide (SWG).
Identifiers
| code_info | Lot number: 23F17C0652 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0650-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.