FDA Device recall Z-0076-2015
Multi-Lumen Central Venous Catheterization Kit
- FDA Device
- Class II
- terminated
- Published 2014-10-22
On 2014-10-22 the FDA classified a Class II recall of Multi-Lumen Central Venous Catheterization Kit by Arrow International, citing arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0076-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-09-18 |
| Published | 2014-10-22 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Arrow International |
| Distribution | CA, IN, KY, LA, MD, NC, NV, NY, OH, PA |
Product
Multi-Lumen Central Venous Catheterization Kit
Reason
Arrow International, Inc. has initiated a voluntary recall for product code AK- 12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct expiration date.
Identifiers
| code_info | Catolog No - AK-12703 lot number RF3039028 |
|---|
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-0076-2015%22
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