AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI: (1) 722006 00884838055513(21) 00884838059115(21) 00884838059191(10) (2) 722012 00884838059054(21) (3) 722028 00884838054202(21)
- 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:
- Potential safety issue with the AD7 and AD7X patient tables (both tilt and non-tilt versions) part of the Philips Allura and Azurion systems. During manual repositioning of the patient tabletop, a finger can get entrapped between the longitudinal guiding rails and the tabletop. This may result in an injury of the finger, applicable for operators and service personnel
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
Product Codes/Lot Numbers:
UDI: (1) 722006 00884838055513(21) 00884838059115(21) 00884838059191(10) (2) 722012 00884838059054(21) (3) 722028 00884838054202(21)
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1080-2025
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