FDA Device recall Z-0690-2018
ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet
- FDA Device
- Class II
- terminated
- Published 2018-02-28
On 2018-02-28 the FDA classified a Class II recall of ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet by Arrow International, citing the kit may contain an incorrect catheter component. Kits that should contain a 40cm catheter may contain a 55cm catheter.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0690-2018 |
| 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 | AZ, CA, GA, MA, MO, NY, VA |
Product
ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet
Reason
The kit may contain an incorrect catheter component. Kits that should contain a 40cm catheter may contain a 55cm catheter.
Identifiers
| code_info | CDC 34041 VPS Lot# 23F17A0037 23F17B0035 |
|---|
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-0690-2018%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.