Devices

Device Recall Basic Extended Pack

Model / Serial
Lot number and expiration date 84855, 8/6/2018 88319, 9/5/2018 88950, 11/15/2018 95760, 1/26/2019 96235, 5/14/2019 98080, 6/19/2019
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
Basic Extended Pack, part number AMS4421(A || Basic Extended Pack, part number AMS4421(B
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
- Recall of Device Recall Basic Extended Pack

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

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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