FDA Device recall Z-1823-2012
Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A T…
- FDA Device
- Class II
- terminated
- Published 2012-06-27
On 2012-06-27 the FDA classified a Class II recall of Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A T… by Arrow International, citing arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1823-2012 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-06-07 |
| Published | 2012-06-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arrow International |
| Distribution | US |
Product
Arrow International, Inc. 7FR 3-Lumen Arrowg+ard Blue Plus(R) Pressure Injectable Central Venous Catheter - Catalog number CDC-42703-XP1A The multiple-lumen pressure injectable catheter permits venous access to central circulation and injection of contrast media. The ARROWg+ard(R) antimicrobial surface is intended to provide protection against catheter-related infections.
Reason
Arrow is recalling the product due to the possibility of voids in the catheter hub which could lead to an interlumen crossover.
Identifiers
| code_info | Lot number RF2033361 |
|---|
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-1823-2012%22
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