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Stryker Communications Recalls
20 recalls on record · January 16, 2013 to April 8, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
April 8, 2026Medical DevicesFDA
Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001
Hazard: Surgical light assembly may not adequate support the weight of the ceiling cover.
October 1, 2025Medical DevicesFDA
Stryker Communications recalls Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034
Hazard: Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
April 17, 2024Medical DevicesFDA
Stryker Communications recalls Chromophare Surgical Light System , REF CH00000001
Hazard: Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.
March 31, 2021Medical DevicesFDA
Stryker Communications recalls S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected with
Hazard: 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 disengage when an electrocautery device is in use.
April 8, 2020Medical DevicesFDA
Stryker Communications recalls Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000
Hazard: 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 suspension of the surgical light falls, it may potentially cause serious injuries to Health Care Providers and/or patients.
September 18, 2019Medical DevicesFDA
Stryker Communications recalls Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment
Hazard: The back cover of the light head was insufficiently assembled and could potentially fall off the light.
September 18, 2019Medical DevicesFDA
Stryker Communications recalls Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical lights are for usage in hospital treatment
Hazard: The back cover of the light head was insufficiently assembled and could potentially fall off the light.
September 11, 2019Medical DevicesFDA
Stryker Communications recalls Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted
Hazard: The mounts on the monitor may have an insufficient weld.
May 29, 2019Medical DevicesFDA
Stryker Communications recalls EDS Light Suspension, Central Axis, a component of the Stryker Visum LED Surgical Lighting System, with the following ca
Hazard: There is a potential the joint in the suspension of the device is insufficiently assembled.
March 7, 2018Medical DevicesFDA
Stryker Communications recalls Berchtold Chromophare Ceiling Mounted Surgical Light System, Catalog #CH13000000. Product Usage: Chromophare surgica
Hazard: The device could have a missing spanner nut and snap ring which could potentially result in the equipment falling.
March 7, 2018Medical DevicesFDA
Stryker Communications recalls Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted
Hazard: The mounts on the monitor may have an insufficient (missing or incomplete) weld.
June 14, 2017Medical DevicesFDA
Stryker Communications recalls Berchtold Chromophare F300 Exam Light CHROMOPHARE examination lights are medical lights used for local illumination of
Hazard: The exam light may have a tolerance issue with the adapter assembly, which could potentially not allow the snap ring to be seated correctly. If this is the case, there could be insufficient mount force that may cause the equipment to fall, resulting in serious injury.
April 5, 2017Medical DevicesFDA
Stryker Communications recalls The Stryker Visum¿ LED Surgical Lighting system is intended to illuminate the operative site during surgical procedures
Hazard: The potential hazard that can arise for the combination of the missing screws and the overloading by the end user is insufficient mount force that causes the equipment to fall.
July 23, 2014Medical DevicesFDA
Stryker Communications recalls BAM (SHAPE) ARM, RIGHT, an articulating, arm bracket that is attached to the service head of boom systems which are used
Hazard: During the use of the SHAPE Arm there is the potential for the monitor mount to come off of the SHAPE Arm if the lock washer and screw are not present.
July 23, 2014Medical DevicesFDA
Stryker Communications recalls BAM (SHAPE) ARM, LEFT, an articulating, arm bracket that is attached to the service head of boom systems which are used
Hazard: During the use of the SHAPE Arm there is the potential for the monitor mount to come off of the SHAPE Arm if the lock washer and screw are not present.
July 23, 2014Medical DevicesFDA
Stryker Communications recalls SHAPE ARM, SINGLE WITH GCX MOUNT, an articulating, arm bracket that is attached to the service head of boom systems whic
Hazard: During the use of the SHAPE Arm there is the potential for the monitor mount to come off of the SHAPE Arm if the lock washer and screw are not present.
July 23, 2014Medical DevicesFDA
Stryker Communications recalls SHAPE ARM, DUAL SH2, an articulating, arm bracket that is attached to the service head of boom systems which are used fo
Hazard: During the use of the SHAPE Arm there is the potential for the monitor mount to come off of the SHAPE Arm if the lock washer and screw are not present.
July 23, 2014Medical DevicesFDA
Stryker Communications recalls SHAPE ARM, SINGLE, an articulating, arm bracket that is attached to the service head of boom systems which are used for
Hazard: During the use of the SHAPE Arm there is the potential for the monitor mount to come off of the SHAPE Arm if the lock washer and screw are not present.
August 28, 2013Medical DevicesFDA
Stryker Communications recalls Stryker Visum 300 Ceiling-mounted Exam Light.
Hazard: Potential incomplete final weld on the drop tube flange.
January 16, 2013Medical DevicesFDA
Stryker Communications, Inc. recalls (l) Visum Halogen Surgical Light, (2) Visum LED Surgical Light, (3) Stryker Flat Panel and Navigation Arm The Spring
Hazard: Stryker has become aware that there is a low likelihood of incomplete engagement of the Spring Arm Circlip during service or replacement of the Spring Arm. If the Spring Arm Circlip is not fully seated, the Spring Arm could separate and fall along with the surgical lights or monitors mounted to the end of the Spring Arm. To date, there have been no serious injuries reported from the incomplete e