FDA Device recall Z-1997-2015
Phleb Pack and Laser Phleb 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 Phleb Pack and Laser Phleb 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-1997-2015 |
| 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
Phleb Pack and Laser Phleb 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 682-1284, 682-299, 682-410, 682-353, 682-377, 682-548 |
|---|
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-1997-2015%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.