FDA Device recall Z-0259-2017
Peri GYN, Kit number PSS2193(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 Peri GYN, Kit number PSS2193(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-0259-2017 |
| 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
Peri GYN, Kit number PSS2193(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: 58336 3/5/2014 61990 8/20/2014 61732 9/10/2014 63878 2/9/2015 65773 2/25/2015 64…Lot Numbers/ Expiration Dates: 58336 3/5/2014 61990 8/20/2014 61732 9/10/2014 63878 2/9/2015 65773 2/25/2015 64610 3/27/2015 68071 8/5/2015 69931 10/26/2015 71918 2/15/2016 73291 2/22/2016 74558 6/14/2016 77064 7/14/2016 78767 9/5/2016 78000 9/8/2016 |
|---|
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-0259-2017%22
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