FDA Device recall Z-1993-2015
Basic Pack - 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 Basic Pack - 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-1993-2015 |
| 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
Basic Pack - 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 693-203, 888-2375, 888-2396, 888-2430, 888-2495, 888-2594 |
|---|
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-1993-2015%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.