RecallRadar

FDA Device recall Z-0174-2017

Dr Mullins Kit, kit number PSS1861(A convenience custom kits used for general surgery in hospital operating room

On 2016-10-26 the FDA classified a Class II recall of Dr Mullins Kit, kit number PSS1861(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

AgencyFDA Device
Recall numberZ-0174-2017
ClassificationClass II
Statusterminated
Initiated2015-04-22
Published2016-10-26
Last updated2026-09-13 11:54 UTC
CompanyWindstone Medical Packaging
DistributionUS

Product

Dr Mullins Kit, kit number PSS1861(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: 65805 2/24/2015 59138 8/31/2015 61015 9/17/2015 65118 10/20/2015 65413 11/3/2015…Lot Numbers/Expiration Dates: 65805 2/24/2015 59138 8/31/2015 61015 9/17/2015 65118 10/20/2015 65413 11/3/2015 66234 11/8/2015 66921 11/29/2015 57959 8/15/2016 69802 9/27/2016 68607 10/5/2016 71901 10/19/2016 71111 12/26/2016 72510 3/14/2017 76252 4/14/2017 76892 4/23/2017 74517 5/15/2017 73799 5/24/2017 75239 7/15/2017 77363 8/25/2017

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-0174-2017%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.