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FDA (Device enforcement)Recalled 2025-03-24class ii

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.: Intera 1.5T Omni/Stellar, Model Number: 781104;

Hazard

The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.

Details from the source

Reason for recall: The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury. Distribution: US: Nationwide Distribution International: Algeria, Andorra, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Botswana, Brazil, Bulgaria, Canada, Cayman Islands, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Ethiopia, Finland, France, Georgia, Germany, Greece, Guadeloupe, Ho Quantity: 26 units (7 US, 19 OUS) Lot/code info: Model Number (REF): 781104; UDI-DI: N/A; All serial numbers.

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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