ProxiDiagnost N90; Model Number: 706110;
Class I - DangerousWhat Should You Do?
- Check if you have this product: Model Number: 706110; UDI-DI: 00884838103221; Serial Number: 10001185, 10001205, 10001220, 10001224, 10001225, 10001227, 10001228, 10001229, 10001230, 10001231, 10001234, 10001235, 10001236, 10001237, 10001239, 10001245, 10001247, 10001248, 10001249, 10001250, 10001251, 10001253, 10001256, 10001257, 10001258, 10001261, 10001262, 10001264, 10001265, 10001266, 10001269, 10001270, 10001271, 10001272, 10001273, 10001274, 10001275, 10001276, 10001277, 10001278, 10001282;
- 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 DMC GmbH
- Reason for Recall:
- Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
ProxiDiagnost N90; Model Number: 706110;
Product Codes/Lot Numbers:
Model Number: 706110; UDI-DI: 00884838103221; Serial Number: 10001185, 10001205, 10001220, 10001224, 10001225, 10001227, 10001228, 10001229, 10001230, 10001231, 10001234, 10001235, 10001236, 10001237, 10001239, 10001245, 10001247, 10001248, 10001249, 10001250, 10001251, 10001253, 10001256, 10001257, 10001258, 10001261, 10001262, 10001264, 10001265, 10001266, 10001269, 10001270, 10001271, 10001272, 10001273, 10001274, 10001275, 10001276, 10001277, 10001278, 10001282;
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0461-2026
Related Recalls
Radiography 7300 C; Model Number: 712037;
Philips Medical Systems DMC GmbH
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
Philips Medical Systems DMC GmbH
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
Precision CRF; Model Number: 706400;
Philips Medical Systems DMC GmbH
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.