Devices

Device Recall Synthes Flex Arm

Model / Serial
Lot numbers 9833185, 9866629, 9888308, 9914323, 9940637, 9982802, H044106, H072780, H144265, H212060, H260544, H260547, H305886, H347867, H430221, H430230
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Switzerland and Japan
Product Description
Flex Arm || Product Usage: || The Synthes Flex Arm is a component of the Synthes Minimally Invasive Support System, which provides secure table mounting for minimally invasive spine surgery. The Flex Arm is designed to hold Synthes Minimally Invasive Retractors, which are connected to the Flex Arm by adapters.
Manufacturer
Synthes, Inc.
1 Event
- Recall of Device Recall Synthes Flex Arm

Manufacturer

Synthes, Inc.

Manufacturer Address
Synthes, Inc., 1302 Wrights Ln E, West Chester PA 19380-3417
Manufacturer Parent Company (2017)
Johnson & Johnson
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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