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Devices
Device Recall Basin Pack
Model / Serial
Lot number and expiration date 84187, 5/14/2018 84938, 6/30/2018 85835, 9/12/2018 86871, 8/14/2019 87444, 9/30/2018 88377, 11/15/2018 88626, 10/8/2018 89025, 12/10/2018 89575, 1/30/2019 94929, 3/6/2019 96912, 5/5/2019 97575, 6/22/2019 97652, 9/27/2019
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
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.
Product Description
Basin Pack, part number AMS2497
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
Recall of Device Recall Basin Pack
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Manufacturer
Windstone Medical Packaging, Inc.
Manufacturer Address
Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
Manufacturer Parent Company (2017)
Windstone Medical Packaging Inc.
Source
USFDA
Language
English
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