Philips Medical Systems recalled 298 Allura Xper FD20 operating room tables on September 3, 2025, due to a faulty BIOS battery. The battery depletes faster than expected, halting system start-up without warning. This recall affects 72 units in the U.S. and 226 units distributed internationally.
The BIOS battery may deplete faster than initially anticipated during the design phase. When the battery is depleted, the start-up process of the system will be halted, and the system will not start. No user messages are shown before the battery is low on power or depleted.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. or your healthcare provider for instructions. Notification method: Letter
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The recalled products include Allura Xper FD20 operating room tables with model numbers 722015, 722023, and 722035. These units were distributed worldwide, including 72 in the U.S. and 226 in countries such as Canada, Germany, and Japan.
The BIOS battery in the tables may deplete more quickly than anticipated. When this occurs, the system fails to start, potentially impacting surgical procedures.
No specific incidents or injuries have been reported at this time. The lack of warning before battery depletion poses serious risks for users.
Stop using the operating room tables immediately. Contact Philips Medical Systems Nederland B.V. or your healthcare provider for further instructions and follow the recall guidelines provided.
For more information, contact Philips Medical Systems Nederland B.V. at the link provided or consult your healthcare provider.
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