Data Foundry

Medical device recalls 2017

Extremity Pack — Class II medical device recall Z-1295-2017

Terminated recall by Windstone Medical Packaging, Inc., reported 2017-03-08, distributed in AZ, CA, CO, CT, FL, GA, IL, IN…. The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES of the custom Aligned Medical Solutions (AMS) kits were rec

Recall numberZ-1295-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmWindstone Medical Packaging, Inc., Billings, MT, United States
Recall initiated2017-01-11
Classified2017-02-28
Reported by FDA2017-03-08
Terminated2017-05-03
DistributedAZ, 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
Quantity810 kits
Reason classessterility
Lot numbers100226, 101400, 84373, 84678, 84896, 84959, 85470, 85505, 85547, 85695, 85846, 86258, 86509, 86663, 86686, 86908, 87155, 87730, 87968, 88008, 88862, 89394, 89546, 89832, 95313, 95453, 95880, 96000, 96383, 96384, 96923, 97709, 99376
Model numbersAMS3240, AMS4764, AMS4788, PSS1798, PSS1842, PSS2706

Product

Extremity Pack, part number AMS3240 Extremity Pack, part number AMS4764 Extremity Pack, part number AMS4788(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1798(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS1842(A Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part numbre PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706 Extremity Pack, part number PSS2706(A Extremity Pack, part number PSS2706(A Extremity Pack, part number PSS2706(A Extremity Pack, part number PSS2706(A

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.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1295-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.