Drug recall
Convenience Kits from Centurion that contain a Medtronic/Covidien Light Glove ED SUTURE KIT VAGINAL DELIVERY…
FDA recall event 74604 · Class II · Centurion Medical Products Corporation
Key facts
| Event ID | 74604 |
|---|---|
| Recall numbers | Z-2250-2016 |
| Recalling firm | Centurion Medical Products Corporation |
| Product type | Devices |
| Products | Convenience Kits from Centurion that contain a Medtronic/Covidien Light Glove ED SUTURE KIT VAGINAL DELIVERY TRAY ENDOSCOPY TRAY MINOR BASIN SET LAPAROSCOPIC BASIN TRAY |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Kits from Centurion contain a Medtronic/Covidien Light Glove that is being recalled by the manufacturer, Medtronic. According to the notice received from Medtronic, the recall was initiated because… |
| Initiation date | Apr 29, 2015 |
| Report date | Jul 27, 2016 |
| Termination date | Nov 3, 2016 |
| City | Williamston |
| State | MI |
| Country | United States |
| FEI number | 3008403546 |
At a glance
- 1–9 Products in this recall
- 1–9 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: