Devices

Device Recall Surgical Pack

Model / Serial
Lot number and expiration date 84577, 8/18/2018 88021, 12/1/2018 95560, 1/18/2019 95673, 1/27/2019
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
Surgical Pack, part number PSS3540(A
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
- Recall of Device Recall Surgical 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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Disclaimer

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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