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Devices
Device Recall General Surgery Pack
Model / Serial
Lot number and expiration date 84680, 5/19/2018 85462, 8/6/2018 86849, 8/16/2018 87483, 8/11/2019
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
General Surgery Pack, part number PSS1380(A
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
Recall of Device Recall General Surgery 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
One device with a similar name
Learn more about the data
here
Device Recall General Surgery Packs
Model / Serial
lot 56402, 57255, 60542, and 61506
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide distribution to Louisiana and Montana.
Product Description
General Surgery Pack, part number 006880-3. This is a custom convenience surgical instrument disposable kit. || There are multiple component in this kit and the recalled item subject to recall is Medtronic Kerlix X-Ray Detectable Laparotomy Sponges.
Manufacturer
Windstone Medical Packaging, Inc.
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