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Devices
Device Recall Anterior Cervical Fusion Pack
Model / Serial
Lot numbers and Expiration dates: 84343, 5/20/2018 88052, 11/11/2018 89579, 11/15/2018 89709, 12/10/2018 94934, 1/4/2019 95441, 6/3/2019
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
Anterior Cervical Fusion Pack, part number AMS2502(A || Anterior Cervical Fusion Pack, part number AMS2502(C
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
Recall of Device Recall Anterior Cervical Fusion 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
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