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Crédits
Devices
Device Recall Knee Arthroscopy Pack
Modèle / numéro de série
Lot number and expiration date 100023, 9/22/2019 100595, 9/1/2019 84529, 5/13/2018 84584, 5/26/2018 84728, 5/25/2018 85250, 7/22/2018 85273, 7/10/2018 85645, 8/1/2018 85845, 8/19/2018 87286, 8/11/2019 87350, 9/21/2018 87967, 9/24/2018 88173, 11/11/2018 88390, 11/21/2018 88627, 12/24/2018 89082, 10/3/2018 89422, 12/16/2018 89511, 11/13/2018 94573, 11/19/2018 94941, 11/20/2018 95452, 5/6/2019 95985, 3/8/2019 97273, 5/22/2019 98169, 6/26/2019 98664, 6/25/2019 98675, 6/23/2019 99375, 6/12/2019
Classification du dispositif
General and Plastic Surgery Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
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.
Description du dispositif
Knee Arthroscopy Pack , part number AMS2610(A || Knee Arthroscopy Pack, part number AMS3236(A || Knee Arthroscopy Pack, part numbre AMS3860
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
Rappel de Device Recall Knee Arthroscopy Pack
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Fabricant
Windstone Medical Packaging, Inc.
Adresse du fabricant
Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
Société-mère du fabricant (2017)
Windstone Medical Packaging Inc.
Source
USFDA
Language
English
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