Drug recall
GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet…
FDA recall event 76363 · Class II · Vascular Solutions, Inc.
Key facts
| Event ID | 76363 |
|---|---|
| Recall numbers | Z-1250-2017 |
| Recalling firm | Vascular Solutions, Inc. |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Jan 12, 2017 |
| Report date | Mar 1, 2017 |
| Termination date | Apr 18, 2018 |
| City | Maple Grove |
| State | MN |
| Country | United States |
| FEI number | 3002827704 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: