Philips North America: Medical Device Recall in 2024 - (Recall #: Z-0955-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

SmartPath to dStream for 1.5T. Model (REF) Numbers 781260, 782112.

Product Classification:

Class II

Date Initiated: January 3, 2024

Date Posted: February 7, 2024

Recall Number: Z-0955-2024

Event ID: 93787

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.

Status: Ongoing

Product Quantity: 37 US; 735 OUS

Code Information:

a. Model No. 781260; UDI-DI 00884838095076. b. Model No. 782112; UDI-DI 00884838098886. All units affected

Distribution Pattern:

Worldwide - US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated