RecallRadar

FDA Device recall Z-1280-2017

Catheter Pack, part number AMS4399(A

On 2017-03-08 the FDA classified a Class II recall of Catheter Pack, part number AMS4399(A by Windstone Medical Packaging, citing the Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterili….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1280-2017
ClassificationClass II
Statusterminated
Initiated2017-01-11
Published2017-03-08
Last updated2026-09-13 11:54 UTC
CompanyWindstone Medical Packaging
DistributionAZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, WA

Product

Catheter Pack, part number AMS4399(A

Reason

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were recalled because gloves may contain splits or holes compromising sterility.

Identifiers

code_info
Lot number and expiration date 84598 4/16/2017 84599 5/8/2018 85277 5/11/2018 85342 5/17/2018 85456 6/3/2018 85…Lot number and expiration date 84598 4/16/2017 84599 5/8/2018 85277 5/11/2018 85342 5/17/2018 85456 6/3/2018 85629 6/11/2018 85630 8/21/2018 87145 10/15/2018 89443 8/23/2018 89892 11/30/2018 95180 8/24/2018 95298 11/21/2018 95789 11/11/2018 96424 12/26/2018 96494 12/17/2018 96945 3/11/2019 97753 4/3/2019 97817 4/12/2019 98124 4/18/2019 98703 5/23/2019 98704 6/7/2019 98940 6/30/2019 99561 6/17/2019 99900 6/29/2019

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-1280-2017%22

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