RecallRadar

FDA Device recall Z-0173-2017

Dr Bragg Vein Tray - RX, kit numbers 007912-5, 007912-6, 007912-7, 007912-8 convenience custom kits used for general surgery in hospital op…

On 2016-10-26 the FDA classified a Class II recall of Dr Bragg Vein Tray - RX, kit numbers 007912-5, 007912-6, 007912-7, 007912-8 convenience custom kits used for general surgery in hospital op… 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-0173-2017
ClassificationClass II
Statusterminated
Initiated2015-04-22
Published2016-10-26
Last updated2026-09-13 11:54 UTC
CompanyWindstone Medical Packaging
DistributionUS

Product

Dr Bragg Vein Tray - RX, kit numbers 007912-5, 007912-6, 007912-7, 007912-8 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: 61836 6/30/2013 58821 9/2/2013 60583 11/1/2013 62371 3/8/2014 65618 4/16/2014 64…Lot Numbers/ Expiration Dates: 61836 6/30/2013 58821 9/2/2013 60583 11/1/2013 62371 3/8/2014 65618 4/16/2014 64076 4/20/2014 67477 7/11/2014 69351 10/2/2014 69593 12/20/2014 72030 2/2/2016 73144 2/17/2016 72643 2/28/2016 74897 5/31/2016 77971 6/16/2016 76042 6/20/2016 56380 6/25/2016

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-0173-2017%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.