FDA Device recall Z-0165-2017

Custom Pack, Kit numbers PSS1300, PSS1471(A, PSS1771, PSS2135(A, PSS2135(B, PSS2207, PSS2412(B, PSS2798, PSS2798(A, PSS2798(B, PSS3054, PSS…

FDA Device
Class II
terminated
Published 2016-10-26

On 2016-10-26 the FDA classified a Class II recall of Custom Pack, Kit numbers PSS1300, PSS1471(A, PSS1771, PSS2135(A, PSS2135(B, PSS2207, PSS2412(B, PSS2798, PSS2798(A, PSS2798(B, PSS3054, PSS… 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-0165-2017
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

Custom Pack, Kit numbers PSS1300, PSS1471(A, PSS1771, PSS2135(A, PSS2135(B, PSS2207, PSS2412(B, PSS2798, PSS2798(A, PSS2798(B, PSS3054, PSS3463, TVS4011NI(J, TVS4028(A, and TVS4070. 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: 60238 4/27/2014 63592 5/22/2014 61110 5/31/2014 64981 6/6/2014 64360 6/6/2014 63… Lot Numbers/ Expiration Dates: 60238 4/27/2014 63592 5/22/2014 61110 5/31/2014 64981 6/6/2014 64360 6/6/2014 63344 6/17/2014 62792 6/18/2014 63990 6/23/2014 61099 8/21/2014 59122 9/20/2014 65818 11/18/2014 72314 11/25/2014 57135 1/21/2015 65766 2/26/2015 73492 3/31/2015 59151 4/24/2015 57576 5/8/2015 70776 5/13/2015 58841 5/15/2015 57136 5/25/2015 59700 7/8/2015 60764 8/7/2015 61177 8/12/2015 61496 8/15/2015 59482 8/19/2015 60670 9/12/2015 60618 9/15/2015 60619 9/20/2015 61098 9/27/2015 65575 10/17/2015 65113 10/18/2015 60828 10/27/2015 62788 11/2/2015 61930 11/4/2015 61354 11/6/2015 66242 11/7/2015 65407 11/8/2015 62515 11/10/2015 65328 11/10/2015 65380 11/16/2015 62064 11/18/2015 61734 11/22/2015 63294 11/28/2015 63296 11/28/2015 63350 12/9/2015 63743 12/11/2015 62511 12/25/2015 63037 12/25/2015 63371 12/28/2015 63295 12/28/2015 64672 1/13/2016 63423 1/16/2016 63746 1/22/2016 63751 1/23/2016 61978 1/28/2016 75438 5/18/2016 57

code_info

Lot Numbers/ Expiration Dates: 60238 4/27/2014 63592 5/22/2014 61110 5/31/2014 64981 6/6/2014 64360 6/6/2014 63…

Lot Numbers/ Expiration Dates: 60238 4/27/2014 63592 5/22/2014 61110 5/31/2014 64981 6/6/2014 64360 6/6/2014 63344 6/17/2014 62792 6/18/2014 63990 6/23/2014 61099 8/21/2014 59122 9/20/2014 65818 11/18/2014 72314 11/25/2014 57135 1/21/2015 65766 2/26/2015 73492 3/31/2015 59151 4/24/2015 57576 5/8/2015 70776 5/13/2015 58841 5/15/2015 57136 5/25/2015 59700 7/8/2015 60764 8/7/2015 61177 8/12/2015 61496 8/15/2015 59482 8/19/2015 60670 9/12/2015 60618 9/15/2015 60619 9/20/2015 61098 9/27/2015 65575 10/17/2015 65113 10/18/2015 60828 10/27/2015 62788 11/2/2015 61930 11/4/2015 61354 11/6/2015 66242 11/7/2015 65407 11/8/2015 62515 11/10/2015 65328 11/10/2015 65380 11/16/2015 62064 11/18/2015 61734 11/22/2015 63294 11/28/2015 63296 11/28/2015 63350 12/9/2015 63743 12/11/2015 62511 12/25/2015 63037 12/25/2015 63371 12/28/2015 63295 12/28/2015 64672 1/13/2016 63423 1/16/2016 63746 1/22/2016 63751 1/23/2016 61978 1/28/2016 75438 5/18/2016 57

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-0165-2017%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.