Recall
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; MAJOR PROCEDURE TRACECART (R),…
DeRoyal Industries Inc · 27 April 2015
- Status
- Recall terminated
- Why, in the FDA's words
- “Surgical kits contain Medtronic Covidien Devon(TM) Light Gloves which were recalled for splits or holes”
- Recall began
- 27 April 2015
- Company
- DeRoyal Industries Inc
- Device type
- Product code (LRO)
What it means
A recall is the FDA's record that a company is correcting or removing a device because of a problem. Many are fixed with a software update or new instructions; the record does not say whether anyone was hurt. See our plain guide to FDA terms.
The record
The FDA publishes this record in its public device database. The summary documents the company filed, when available, are linked from the FDA's page.