Stryker Communications Chromophare Surgical Light System, REF: CH00000001 recall — FDA Z-2620-2025
Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
Overview of recall records associated with Stryker Communications, including dates, categories and classifications where available.
Classification mix: Class II: 7.
Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
The manufacturer has become aware that there is a likelihood that the S-Series Equipment Management System Capacitive Touch Controls on the MFRs rotational electrical magnetic brakes may…
The firm has become aware that there is a likelihood that a missing snap ring or spanner nut may result in an insufficient mount force that causes the surgical light to fall. If the…
The back cover of the light head was insufficiently assembled and could potentially fall off the light.
The back cover of the light head was insufficiently assembled and could potentially fall off the light.
The mounts on the monitor may have an insufficient weld.
There is a potential the joint in the suspension of the device is insufficiently assembled.
This page summarizes recall records in which the official source identifies Stryker Communications 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.