RecallRadar

FDA Device recall Z-0141-2017

Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(A convenience custom kits used for general surgery in hospital operati…

On 2016-10-26 the FDA classified a Class II recall of Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(A convenience custom kits used for general surgery in hospital operati… 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-0141-2017
ClassificationClass II
Statusterminated
Initiated2015-04-22
Published2016-10-26
Last updated2026-09-13 11:54 UTC
CompanyWindstone Medical Packaging
DistributionUS

Product

Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(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: 62090 11/18/2015 64503 11/20/2015 65165 11/9/2015 66042 7/15/2016 68496 9/18/2016…Lot Numbers; Expiration Dates: 62090 11/18/2015 64503 11/20/2015 65165 11/9/2015 66042 7/15/2016 68496 9/18/2016 75702 7/4/2017 76407 2/4/2017 78060 2/23/2017 78683 9/8/2017 79143 11/3/2017

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-0141-2017%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.