Operating Room Table BIOS Battery Depletion Prevents System Startup
The BIOS battery in Philips Allura Xper FD20 operating room tables may deplete faster than expected, preventing system startup. No warning messages appear before depletion.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Class II medical device recall for a risk-of-harm product (surgical operating table). Per the rubric, risk-of-harm products without reported injuries or illnesses score at severity 3 (High). No incidents have been reported.
Plain-English summary
Philips Medical Systems Nederland B.V. is recalling the Allura Xper FD20 Biplane Operating Room Table due to a potential BIOS battery issue. The recall affects 4 units with model numbers 722020 and 722025—2 units in the United States and 2 units internationally.
The BIOS battery in these operating room tables may deplete faster than initially anticipated during the product design phase. When depleted, the startup process halts and the system will not start. No user messages or warnings appear before the battery becomes low or depleted, preventing advance notification to operators.
Healthcare facilities and surgical centers using the affected models should immediately verify their device status and contact Philips Medical Systems Nederland B.V. for further instructions regarding system remediation or battery replacement.
The recalled product
- Product
- Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Hazard
- bios-battery-depletion
- startup-failure
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (8)
- Model Numbers: (1) 722020
- (2) 722025
- UDI-DI: (1) N/A
- (2) 00884838059108
- Serial Numbers: (1) 4
- (2) 2
- 3
- 6
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- SevereMedline spinal anesthesia kits recalled for bupivacaine quality issues
FDA (Devices) · 2026-06-03
- HighGE CARESCAPE Telemetry Server may lose patient ECG and oxygen saturation monitoring
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- SevereMedline Spinal Trays Recalled Due to Quality and Efficacy Concerns
FDA (Devices) · 2026-06-03
- HighPhilips Azurion and Allura Imaging Systems Recalled for Hard Drive Degradation
FDA (Devices) · 2026-06-03