FDA Device recall Z-0228-2017
Lower Extremity Pack, Kit number AMS1375(A, AMS2540, AMS2540(A, and AMS4669. convenience custom kits used for general surgery in hospital o…
- FDA Device
- Class II
- terminated
- Published 2016-10-26
On 2016-10-26 the FDA classified a Class II recall of Lower Extremity Pack, Kit number AMS1375(A, AMS2540, AMS2540(A, and AMS4669. convenience custom kits used for general surgery in hospital o… 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-0228-2017 |
| 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
Lower Extremity Pack, Kit number AMS1375(A, AMS2540, AMS2540(A, and AMS4669. 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: 62895 3/16/2014 61290 3/30/2014 57472 4/2/2014 59889 8/8/2014 61313 8/27/2014 622…Lot numbers/Expiration dates: 62895 3/16/2014 61290 3/30/2014 57472 4/2/2014 59889 8/8/2014 61313 8/27/2014 62201 10/18/2014 63202 12/12/2014 64163 12/17/2014 65489 3/8/2015 68367 4/13/2015 66793 4/30/2015 69272 9/14/2015 70920 9/30/2015 71438 11/4/2015 66044 11/8/2015 64134 11/10/2015 65690 11/17/2015 71985 11/30/2015 65282 12/1/2015 68490 12/21/2015 69186 12/21/2015 71052 12/25/2015 67699 12/27/2015 67960 12/30/2015 72484 5/28/2016 69442 9/21/2016 80467 10/31/2016 |
|---|
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-0228-2017%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.