GrebSet Micro-Introducer Kit — Class II medical device recall Z-1250-2017
Terminated recall by Vascular Solutions, Inc., reported 2017-03-01, distributed nationwide. Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires that have a shelf life shorter than
| Recall number | Z-1250-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vascular Solutions, Inc., Maple Grove, MN, United States |
| Recall initiated | 2017-01-12 |
| Classified | 2017-02-23 |
| Reported by FDA | 2017-03-01 |
| Terminated | 2018-04-18 |
| Distributed | Nationwide (US) |
| Quantity | 633 |
| Lot numbers | 581212, 584392, 594115, 597202 |
| Model numbers | 7941 |
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 for recall
Four Lots of GrebSet Micro-introducer Kits, model 7941, contain guidewires that have a shelf life shorter than the kit expiration date.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1250-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.