{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "149650", "product_res_number": "Z-0155-2017", "event_date_initiated": "2015-04-22", "event_date_created": "2016-10-20", "recall_status": "Terminated", "event_date_terminated": "2016-10-25", "res_event_number": "71968", "product_code": "FSY", "product_description": "Breast Augmentation Pack, Kit part number AMS1786, AMS1786(A, AMS2790, AMS3324, AMS3324(A, and PSS3430.\nconvenience custom kits used for general surgery in hospital operating room", "code_info": "Lot numbers/Expiration dates:  59278\t10/2/2013 58407\t10/14/2013 62436\t12/4/2013 62922\t12/18/2013 60740\t5/20/2014 63467\t6/2/2014 62067\t6/7/2014 64703\t6/10/2014 61619\t6/14/2014 64110\t6/14/2014 63539\t6/29/2014 65271\t7/8/2014 65364\t7/11/2014 65837\t7/31/2014 70246\t9/3/2014 70351\t9/4/2014 69850\t9/7/2014 67400\t9/11/2014 69434\t9/18/2014 71639\t9/18/2014 68310\t9/30/2014 72944\t10/1/2014 71948\t10/9/2014 71949\t10/22/2014 65894\t2/7/2015 68624\t3/12/2015 77600\t8/12/2015 76292\t8/14/2015 72862\t10/5/2015 73989\t10/7/2015 67704\t12/5/2015 73680\t1/3/2016 74974\t1/7/2016 76004\t1/9/2016 75570\t1/17/2016 73628\t1/24/2016 73982\t2/3/2016 74027\t2/24/2016 74377\t3/26/2016 75655\t3/29/2016 79047\t4/5/2016 78542\t4/14/2016 78888\t4/27/2016 77381\t4/30/2016 57192\t5/30/2016 57138\t6/4/2016 78207\t6/20/2016 71656\t8/3/2016 75175\t8/19/2016 77224\t8/23/2016 74582\t9/9/2016 78973\t10/28/2016 79324\t11/16/2016 79137\t11/25/2016", "firm_fei_number": "1000125955", "recalling_firm": "Windstone Medical Packaging, Inc.", "address_1": "1602 4th Ave N", "city": "Billings", "state": "MT", "postal_code": "59101-1521", "additional_info_contact": "Vicki Davis\n406-259-6387", "reason_for_recall": "The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.", "root_cause_description": "Unknown/Undetermined by firm", "action": "Aligned Medical Solutions (AMS) sent the Medtronic Urgent Medical Device for Devon Light Glove letter, dated April 23, 2015 to all affected consignees.\n\nConsignees were informed that the sterile kits assembled and distributed by AMS contain the recalled Devon COVER LIGHT HANDLE DISPOSABLE Glove (AMS part #13140 or Medtronic part # 571711) due to splits or holes. \n\nConsignees were advised to identify any remaining affected kits and follow the over-labeling instruction. At the time the kit is opened for use, any light gloves should be identified and disposed of pursuant to the medical waste policies in effect at your institution. \n\nAMS can provide replacement product if needed or you can contact your local Medtronic sales rep for sterile replacements as well.\n\nDue to the manufacturing process and finished sterilized packs in inventory, or at your facility, over labeling of inventory and/or future shipment affected by this recall will be labeled with a sticker attached to each pack. This sticker will read:\n\nRECALL NOTICE\nMedtronic announced the recall l of Devon Light Glove contained in this kit\nafter it was sealed and sterilized. All other components in the kit are not\naffected by this recall.\n\n1. At the time the kit is opened for use any Light Glove manufactured by Medtronic should be identified and set aside\n\n2. The recalled light glove should be rendered unusable to protect against inadvertent use and disposed of pursuant to the medical waste policies in effect at your institution.\n\nConsignees should complete the attached Reply Form and fax to AMS at 406-256-9875.\n\nFor any questions about this recall, please call 321-527-7714.\nFor questions regarding this recall call 404-259-6387.", "product_quantity": "1498 kits", "distribution_pattern": "Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.", "openfda": { "k_number": [ "K892808", "K914076", "K100702", "K973466", "K990656", "K021585", "K943288", "K961843", "K904965", "K072072", "K142076", "K132307", "K896674", "K093009", "K122875", "K854922", "K131893", "K974084", "K083066", "K140461", "K024132", "K060802", "K102758", "K974433", "K860739", "K781887", "K132747", "K944855", "K030906", "K891756", "K132551", "K042395", "K040015", "K090378", "K101537", "K071698", "K873786", "K820681", "K120392", "K140460", "K002463", "K982063", "K891757", "K070442", "K142984", "K900211", "K902864", "K000639", "K771865", "K080857", "K040735", "K011693", "K140812", "K963682", "K901830", "K965130", "K093010", "K140930", "K063333", "K061317", "K922836", "K984611", "K083323", "K993242", "K954169", "K992090", "K981081", "K915285", "K991527", "K042382", "K010716", "K031979", "K780666", "K031068" ], "registration_number": [ "3023808059", "3031700059", "2031963", "3011644607", "3025628903", "3009061550", "3042992004", "9710585", "9617655", "3006223081", "3000286616", "1000122786", "3003574554", "3007591382", "3030516433", "3007238566", "3027847726", "3012165496", "1066635", "3009028104", "3012092534", "3029970239", "1017294", "9612030", "3030558088", "3042991836", "3012272052", "1423537", "1225473", "3009542956", "1836161", "3002821232", "3031563141", "3015468226", "1043572", "3006437518", "1066270", "9710055", "9680506", "9710098", "8010153", "3021839632", "3015223105", "3005698350", "3029936435", "3007682310", "3026390991", "3020703842", "3015131225", "3010726901", "3009129579", "3010041511", "3011580044", "3011574775", "3035641086", "3011137372", "9611503", "3011910987", "3044829820", "1054713", "3002532594", "9681407", "3033527731", "1921846", "3007143268", "1825014", "3042970964", "3017970309" ], "fei_number": [ "1000114111", "3003779679", "3023808059", "1000396729", "3005747797", "3031700059", "1000214453", "3011644607", "3002957101", "3025628903", "3009061550", "3002750084", "3042992004", "3006223081", "3001236905", "3000286616", "1000122786", "3002939620", "3003574554", "3007591382", "3030516433", "3007238566", "3002808335", "3027847726", "3012165496", "3009028104", "3029970239", "3003184737", "1017294", "3030558088", "3042991836", "3012272052", "1000125341", "3009542956", "3002975342", "3002821232", "3031563141", "3015468226", "1043572", "3006437518", "3002465150", "3001237319", "3015223105", "3005698350", "3029936435", "3026390991", "3020703842", "3015131225", "3010726901", "3009129579", "3010041511", "3011580044", "3011574775", "1000182014", "3035641086", "3000957797", "3002806934", "3011910987", "3044829820", "3025504317", "3006125657", "3002532594", "3033527731", "1921846", "3007143268", "1825014", "3042970964", "3017970309" ], "device_name": "Light, Surgical, Ceiling Mounted", "medical_specialty_description": "General, Plastic Surgery", "regulation_number": "878.4580", "device_class": "2" } } ] }