Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model Numbers: (1) 722020, (2) 722025; UDI-DI: (1) N/A, (2) 00884838059108; Serial Numbers: (1) 4, (2) 2, 3, 6;
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Allura Xper FD20 Biplane OR Table; Model Numbers: (1) 722020, (2) 722025; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Product Codes/Lot Numbers:
Model Numbers: (1) 722020, (2) 722025; UDI-DI: (1) N/A, (2) 00884838059108; Serial Numbers: (1) 4, (2) 2, 3, 6;
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0007-2026
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