FDA Device recall Z-1250-2017
GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide
- FDA Device
- Class II
- terminated
- Published 2017-03-01
On 2017-03-01 the FDA classified a Class II recall of GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide by Vascular Solutions, citing four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires that have a shelf life shorter than the kit expiration date.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1250-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-01-12 |
| Published | 2017-03-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Vascular Solutions |
| Distribution | US |
Product
GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer kit is intended to facilitate the percutaneous placement of guidewires in the vascular system and for delivery of contrast media to vascular sites.
Reason
Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires that have a shelf life shorter than the kit expiration date.
Identifiers
| code_info | Lot Numbers: 581212, 584392, 594115, 597202 |
|---|
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-1250-2017%22
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