Overview of recall records associated with Ra Medical Systems, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Due to footswitch not meeting required specification for protection from ingress of solids or liquids. If spilling of liquids near or on the footswitch, it may fail in the 'on' position and…
Due to the taller wheel mounting on the laser, the laser may fall over potentially causing user or patient injury.
This page summarizes recall records in which the official source identifies Ra Medical Systems, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
