FDA Device recall Z-0283-2017
Vein Kit - No Introducer TVS4027-NI(A convenience custom kits used for general surgery in hospital operating room
- FDA Device
- Class II
- terminated
- Published 2016-10-26
On 2016-10-26 the FDA classified a Class II recall of Vein Kit - No Introducer TVS4027-NI(A convenience custom kits used for general surgery in hospital operating room by Windstone Medical Packaging, citing the Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0283-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-04-22 |
| Published | 2016-10-26 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Windstone Medical Packaging |
| Distribution | US |
Product
Vein Kit - No Introducer TVS4027-NI(A convenience custom kits used for general surgery in hospital operating room
Reason
The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.
Identifiers
| code_info | Lot Numbers/ Expiration Dates: 60996 8/3/2015 59383 8/20/2015 63706 11/11/2015 65733 11/30/2015 65404 12/26/2015…Lot Numbers/ Expiration Dates: 60996 8/3/2015 59383 8/20/2015 63706 11/11/2015 65733 11/30/2015 65404 12/26/2015 58253 7/23/2016 58476 8/30/2016 70957 11/6/2016 71370 12/11/2016 72254 1/8/2017 76639 11/19/2017 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0283-2017%22
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