Devices

Device Recall MicroChoice

Model / Serial
Units under recall include the following serial numbers: 3582 thru 3681, 3685 thru 3733, 3739 thru 3766, 3768, 3800 thru 3809 (74 units)
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide, worldwide.
Product Description
Product is packed in a pouch which is labeled as MicroChoice FOOTSWITCH Linvatec LINVATEC CORPORATION LARGO, FL 33773 USA 5020-053
Manufacturer
Linvatec Corp DBA Linvatec/Hal
1 Event
- Recall of Device Recall MicroChoice

Manufacturer

Linvatec Corp DBA Linvatec/Hal

Manufacturer Address
Linvatec Corp DBA Linvatec/Hal, 11311 Concept Blvd., Largo FL 33773
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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