Quick Facts at a Glance
- Recall Date
- September 3, 2025
- Hazard Level
- HIGH
- Brand
- Philips
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Philips
- Product type
- Surgical/Operating Room Table
- Model numbers
- 722015, 722023, 722035
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
September 3, 2025
Reported by FDA DEVICE
October 8, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
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
About This Product
The Allura Xper FD20 OR Table is a surgical table used in operating rooms to position patients during procedures.
Why This Is Dangerous
A BIOS battery may deplete faster than designed, causing startup to fail without warning, delaying or preventing procedures.
Industry Context
This recall is not described as part of a broader industry pattern.
Real-World Impact
Hospitals may experience delayed surgeries and need to halt procedures until remediation is completed. The recall may affect procurement and service scheduling.
Practical Guidance
How to identify if yours is affected
- Identify model numbers 722015, 722023, 722035
- Check serial numbers listed on the recall materials
- Review recall letter for remediation steps
- Contact Philips or your healthcare provider for instructions and scheduling
Where to find product info
Recall notice and serial/UDI details are in the FDA recall page and manufacturer communications
What timeline to expect
Remediation timelines are not specified in the notice. Expect instructions by letter from Philips.
If the manufacturer is unresponsive
- Escalate to hospital risk management and procurement offices
- Contact FDA recall system if the manufacturer is unresponsive
- Document all attempts to contact the manufacturer and retain copies of correspondence
How to prevent similar issues
- Establish a procedure to verify device model and serial numbers during onboarding and service.
- Maintain up-to-date contact channels with manufacturers for recalls.
- Monitor for recall notifications via hospital memory and vendor portals.
- When buying surgical tables, verify BIOS battery reliability and review recall history
Documentation advice
Keep the recall letter, serial numbers, model numbers, UDI-DI values, and any replacement or service confirmations.
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Product Details
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.
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- 298 total units recalled worldwide; 72 in the US and 226 outside the US
- Model numbers affected: 722015, 722023, 722035
- Hazard: BIOS battery depletion can halt startup with no warning
- Remedy: Stop use and await recall instructions by letter
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Safety Guide
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