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Devices
Device Recall Universal Pack
Model / Serial
Lot number and expiration date 87597, 2/28/2017 88967, 4/30/2017
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
Universal Pack, part number AMS2036
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
Recall of Device Recall Universal 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
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Device Recall UNIVERSAL PACK
Model / Serial
Code:9001587 Lots: 141115774 exp. 11/30/15 141115774 exp. 11/30/15 150116694 exp. 2/28/16 150217474 exp. 2/28/16 150317624 exp. 5/31/16 150418305 exp. 5/31/16 150518651 exp. 5/31/16
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Distributed Only in Puerto Rico.
Product Description
UNIVERSAL PACK 3/CS || Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. || .
Manufacturer
Customed, Inc
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