FDADecember 4, 2015device

Synaptive Medical BrightMatter Navigator System (Guide System). Part number SYN-0026. The Guide system is comprised of a cart labelled SYN-0024 and a cart labelled SYN-0025, Operator Cart. A planning and intraoperative guidance system to enable open and percutaneous computer assisted surgery. The...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Out of tolerance for radio frequency emissions. At the 150-1000MHz frequency, the testing indicated the BrightMatter Navigation system was up to 20dB uV/meter higher than the applicable IEC 60601-1-2:2007 (Ed3.0) standard specification.

What to do

FDA enforcement status: Terminated

Brands named

synaptive medicalsynaptive

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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