FDA Device recall Z-0653-2018
Pressure Injectable ARROWg+ard Blue PLUS 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 Pressure Injectable ARROWg+ard Blue PLUS 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-0653-2018 |
| 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
Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product code: ASK-45703-PHF2; Exp. Dates Feb 2018 - Nov 2018
Reason
These finished good kits may contain the incorrect Springwire Guide (SWG).
Identifiers
| code_info | Lot number: 23F17D0182 |
|---|
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-0653-2018%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.