CLASS II Device recall · Reported 8 Mar 2017 · FDA Enforcement Report

Plastic Kit recalled by Windstone Medical Packaging

Windstone Medical Packaging is recalling Plastic Kit, distributed in 26 states. The recall was initiated on 11 Jan 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot number and expiration date 86626, 9/3/2017 87202, 9/16/2017 87481, 9/9/2017 87924, 9/17/2017 88217, 10/31/2017 88819, 10/27/2017 89271, 10/11/2017 89539, 12/7/2017 95831, 1/9/2018 96460, 4/12/2018 98055, 6/30/2018 98962, 6/22/2018 99088, 9/15/2018
Quantity recalled580 kits

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1360-2017
FDA event ID
76280
Recalling firm
Windstone Medical Packaging, Billings, MT
Classification
Class II
Status
Terminated
Recall initiated
11 Jan 2017
FDA classified
28 Feb 2017
Reported
8 Mar 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material

Timeline

11 Jan 2017Recall initiated by company
28 Feb 2017Classified by FDA+48 days
8 Mar 2017Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Plastic Kit, part number CMP1084(C

Where it was distributed

Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.

ArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIllinoisIndianaKansasLouisianaMassachusettsMarylandMichiganMinnesotaMissouriNorth CarolinaNorth DakotaNebraskaNew JerseyNevada

Questions about this recall

Is Plastic Kit recalled?

Yes. Windstone Medical Packaging recalled Plastic Kit on 11 Jan 2017. The recall is Class II and its status is Terminated. Recall number Z-1360-2017.

Why was it recalled?

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.

Which lots are affected?

Lot number and expiration date 86626, 9/3/2017 87202, 9/16/2017 87481, 9/9/2017 87924, 9/17/2017 88217, 10/31/2017 88819, 10/27/2017 89271, 10/11/2017 89539, 12/7/2017 95831, 1/9/2018 96460, 4/12/2018 98055, 6/30/2018 98962, 6/22/2018 99088, 9/15/2018

Where was it sold?

Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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