Devices

Device Recall FemoStop Reprocessed Femoral Compression Device

Model / Serial
Lot: 869509, 878402, 878439, 879762, 879990, 880274.
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
Devices were distributed to 8 consignees (end users/hospitals) located in VA, CA, FL, MI, WA.
Product Description
ASCENT HEALTHCARE SOLUTIONS. Reprocessed Femoral Compression Device, Model 11165.
Manufacturer
Ascent Healthcare Solutions, Inc.
1 Event
- Recall of Device Recall FemoStop Reprocessed Femoral Compression Device

Manufacturer

Ascent Healthcare Solutions, Inc.

Manufacturer Address
Ascent Healthcare Solutions, Inc., 5307 Great Oak Drive, Lakeland FL 33815-3113
Manufacturer Parent Company (2017)
Stryker
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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