FDA Device recall Z-0235-2017
Major Ortho Pack, kit number 002647-12 and 002647-13 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 Major Ortho Pack, kit number 002647-12 and 002647-13 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-0235-2017 |
| 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
Major Ortho Pack, kit number 002647-12 and 002647-13 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: 59180 8/13/2013 58144 11/7/2013 63191 12/3/2013 62098 12/6/2013 61064 12/13/2013…Lot Numbers/ Expiration Dates: 59180 8/13/2013 58144 11/7/2013 63191 12/3/2013 62098 12/6/2013 61064 12/13/2013 61592 12/16/2013 63809 12/17/2013 62398 12/19/2013 60127 12/20/2013 59454 1/25/2014 66802 1/31/2014 67030 1/31/2014 59839 2/16/2014 61296 2/21/2014 65291 2/28/2014 68567 9/5/2014 62930 9/20/2014 67877 9/21/2014 64458 9/30/2014 71056 10/11/2015 68946 10/26/2015 69206 5/10/2016 69631 5/23/2016 70482 5/29/2016 71057 6/4/2016 57292 6/11/2016 57780 6/23/2016 |
|---|
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-0235-2017%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.