FDA Device recall Z-1082-2015
ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit
- FDA Device
- Class II
- terminated
- Published 2015-02-18
On 2015-02-18 the FDA classified a Class II recall of ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit by Arrow International, citing foreign material found within the kits. The foreign material, white or black particles and/or thread, is visible and can beidentified by the user.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1082-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-01-02 |
| Published | 2015-02-18 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arrow International |
| Distribution | US |
Product
ARROWg+ard Blue PLUS Pressure Injectable Two-Lumen CVC Kit. The Multiple-Lumen Catheter permits venous access to the central circulation by way of the femoral jugular, or subclavian veins.
Reason
Foreign material found within the kits. The foreign material, white or black particles and/or thread, is visible and can beidentified by the user.
Identifiers
| code_info | product number CDC-42802-P1A, lot number 23F14A0063 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1082-2015%22
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