RecallRadar

FDA Device recall Z-1322-2017

Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C

On 2017-03-08 the FDA classified a Class II recall of Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C 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-1322-2017
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

Knee Scope Pack, part number AMS2498(A Knee Scope Pack, part number AMS2498(B Knee Scope Pack, part number AMS2498(C

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 84341, 5/27/2018 85494, 7/21/2018 86719, 9/2/2018 86872, 8/19/2018 87445, 8/2/201…Lot number and expiration date 84341, 5/27/2018 85494, 7/21/2018 86719, 9/2/2018 86872, 8/19/2018 87445, 8/2/2018 88048, 11/22/2018 89163, 11/19/2018 94930, 1/5/2019

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-1322-2017%22

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