Synthes, Inc.: Medical Device Recalls in 2018

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by Synthes, Inc. in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

LCP Drill Sleeve 1.5 Drill Bit 1.1mm Part Number 03.114.001 Used in LCP Modular Mini Fragment System, for fixation of small bones and small bone fragments
Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
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.