FDA Device recall Z-1996-2015
Endovenous Kit, Endo Pack and Endovenous Laser Kit - contains Devon Light Glove Used during surgery
- FDA Device
- Class II
- completed
- Published 2015-07-15
On 2015-07-15 the FDA classified a Class II recall of Endovenous Kit, Endo Pack and Endovenous Laser Kit - contains Devon Light Glove Used during surgery by Stradis Healthcare, citing convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1996-2015 |
| Classification | Class II |
| Status | completed |
| Initiated | 2015-04-20 |
| Published | 2015-07-15 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stradis Healthcare |
| Distribution | US |
Product
Endovenous Kit, Endo Pack and Endovenous Laser Kit - contains Devon Light Glove Used during surgery
Reason
Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.
Identifiers
| code_info | Pack 682-156, 682-1548, 682-931, 682-493, 682-263, 682-931, 682-1419, 682-493, 682-044 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1996-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.