Data Foundry

Medical device recalls 2017

Breast Augmentation Pack — Class II medical device recall Z-1276-2017

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-1276-2017
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
Quantity1,436 kits
Reason classessterility
Lot numbers100634, 83241, 83757, 84174, 84249, 84496, 84521, 84904, 84910, 85071, 85126, 85162, 85565, 85634, 85820, 85831, 85985, 86062, 86141, 86656, 86797, 86862, 87093, 87110, 87747, 88532, 89014, 89155, 89244, 89569, 89770, 89932, 94601, 95184, 95185, 95224, 95265, 95623, 95793, 96299 and 11 more
Model numbersAMS1786, AMS2790, AMS3324, AMS4382, AMS4392, PSS3430

Product

Breast Augmentation Pack, part number AMS1786(A Breast Augmentation Pack, part number AMS2790(A Breast Augmentation Pack, part number AMS3324(B Breast Augmentation Pack, part number AMS4382 Breast Augmentation Pack, part number AMS4382(A Breast Augmentation Pack, part number AMS4382(B Breast Augmentation Pack, part number AMS4392 Breast Augmentation Pack, part number PSS3430

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-1276-2017. 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.