Stryker Communications Recalls

2 recalls found for Stryker Communications. Check if any of your products are affected.

Health & Personal Care
HIGH
FDA DEVICE

Stryker CHROMOPHARE Softlit Ring Surgical Light System Recalled for Ceiling Cover Weight Risk (2026)

Stryker Communications recalled 6,170 CHROMOPHARE Softlit Ring Surgical Light Systems distributed worldwide after confirming the ceiling cover weight may not be adequately supported. Hospitals should stop using the device immediately and follow recall instructions from the manufacturer. The recall is classified as Class II and is active as of February 23, 2026.

Stryker Communications
Surgical light
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Health & Personal Care
HIGH
FDA DEVICE

Stryker Communications Recalls 40 Medical Light Systems Over Powder Coating Chip Risk (2025)

Stryker Communications recalls 40 surgical light systems nationwide after reports of stress lines in the powder coating. The devices include CH00000001 and the SLX to Oculan NFC Upgrade Kit, P60034. The recall is active as of July 15, 2025. Patients and healthcare providers should stop using the devices immediately and follow manufacturer recall instructions.

Stryker Communications
Surgical lights
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Brand Statistics

Total Recalls
2
Pages
1

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