Drug recall
Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves: ANGIO TRAY, REF 50-12127; NEURO…
FDA recall event 71294 · Class II · DeRoyal Industries Inc
Key facts
| Event ID | 71294 |
|---|---|
| Recall numbers | Z-1837-2015 |
| Recalling firm | DeRoyal Industries Inc |
| Product type | Devices |
| Products | Custom Surgical Kits containing Medtronic Covidien Devon(TM) Light Gloves: ANGIO TRAY, REF 50-12127; NEURO SPINE TRAY, LAP CHOLE TRACECART(R), REF 53-1931; MINOR PROCEDURE TRACECART (R), REF 53-1932… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were recalled for splits or holes |
| Initiation date | Apr 27, 2015 |
| Report date | Jul 1, 2015 |
| Termination date | Dec 29, 2015 |
| City | Powell |
| State | TN |
| Country | United States |
| FEI number | 1043214 |
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: