Devices

Foot Pack

Model / Serial
Lot Numbers/ Expiration Dates: 73044 1/27/2016 74133 4/16/2016 76510 10/9/2016
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
Product Description
Foot Pack, Kit number AMS3637 || convenience custom kits used for general surgery in hospital operating room
Manufacturer
Windstone Medical Packaging, Inc.
1 Event
- Recall of Foot 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

2 devices with a similar name

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Device Recall Foot Pack

Model / Serial
Lot number and expiration date 84442, 5/17/2017 84757, 5/17/2017
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
Foot Pack, part number AMS3637
Manufacturer
Windstone Medical Packaging, Inc.

Unomedical ConvaTec Frazier Suction Handle (included in Foot Pack Health and Lower Extremity Proc...

Model / Serial
Unomedical ConvaTec Frazier Suction Handle (included in Foot Pack Health and Lower Extremity Procedure Packs)Frazier Suction HandleProduct Code: UM1912Lot Number: CGCA06-01Foot Pack Health E Care Procedure PackProduct Code: SOPSYML03DLot Numbers: CS1739694, CS1740778, CS1743999, CS1747123 and CS1857459ARTG Number: 137395Lower Extremity Procedure PackProduct Code: SOPMESV06GLot Numbers: CS1741061, CS1742774 and CS1748561ARTG Number 136870
Manufacturer
Medline International Two Australia Pty Ltd

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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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