Philips Medical Systems Nederland B.V. recalled 298 Allura Xper FD20 OR Tables worldwide after a BIOS battery depletion risk could prevent the system from starting. The battery may run down faster than designed, halting startup with no warning. Hospitals and clinicians should stop using the devices immediately and await recall instructions by letter.
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 Allura Xper FD20 OR Table is a surgical table used in operating rooms to position patients during procedures.
A BIOS battery may deplete faster than designed, causing startup to fail without warning, delaying or preventing procedures.
This recall is not described as part of a broader industry pattern.
Hospitals may experience delayed surgeries and need to halt procedures until remediation is completed. The recall may affect procurement and service scheduling.
Recall notice and serial/UDI details are in the FDA recall page and manufacturer communications
Remediation timelines are not specified in the notice. Expect instructions by letter from Philips.
Keep the recall letter, serial numbers, model numbers, UDI-DI values, and any replacement or service confirmations.
Model numbers: 722015, 722023, 722035. Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563. Distribution: Worldwide, including 72 US units and 226 units outside the US. Quantity: 298 units. Manufacturer: Philips Medical Systems Nederland B.V. Recall Date: 2025-09-03. Status: Active.
No injuries or incidents have been reported.
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