FDA Device recall Z-0265-2017
Podiatry Pack, Kit number AMS1541, AMS2778, PSS2645, and PSS3422 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 Podiatry Pack, Kit number AMS1541, AMS2778, PSS2645, and PSS3422 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-0265-2017 |
| 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
Podiatry Pack, Kit number AMS1541, AMS2778, PSS2645, and PSS3422 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 Number/ Expiration Date: 61268 4/17/2014 58664 4/10/2015 59825 8/30/2015 61858 11/9/2015 64825 11/10/2015 6…Lot Number/ Expiration Date: 61268 4/17/2014 58664 4/10/2015 59825 8/30/2015 61858 11/9/2015 64825 11/10/2015 64826 11/15/2015 66761 11/20/2015 64827 11/21/2015 63483 11/23/2015 59800 11/24/2015 63482 12/6/2015 62873 12/18/2015 65631 12/30/2015 64536 1/5/2016 63481 1/6/2016 63800 1/7/2016 66762 2/5/2016 66763 3/1/2016 67345 6/17/2016 75666 6/25/2016 68684 6/26/2016 66755 7/5/2016 78206 7/30/2016 67334 8/9/2016 60594 8/19/2016 68146 9/15/2016 69196 9/16/2016 70378 9/27/2016 70812 10/17/2016 71784 10/19/2016 71471 11/6/2016 72148 12/3/2016 71157 12/20/2016 71970 12/21/2016 74621 1/14/2017 72889 1/21/2017 73855 1/30/2017 73854 2/5/2017 72495 2/8/2017 72725 3/5/2017 75398 4/19/2017 74872 4/24/2017 76184 4/27/2017 75108 4/29/2017 74121 5/9/2017 75399 5/16/2017 77316 7/12/2017 77104 7/28/2017 77416 8/3/2017 77417 8/9/2017 77407 8/24/2017 77408 8/24/2017 77775 9/2/2017 78643 10/3/2017 76478 10/25/2017 80532 12/6/2017 79831 12/18/2017 |
|---|
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-0265-2017%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.