Philips North America: Medical Device Recall in 2024 - (Recall #: Z-0812-2024)

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 No. 781260, 782112

Product Classification:

Class III

Date Initiated: December 29, 2023

Date Posted: January 31, 2024

Recall Number: Z-0812-2024

Event ID: 93788

Reason for Recall:

An incorrect electrical shock warning label may have been placed on the Liquid Cooling Cabinet (LCC) of affected MR systems. The caution symbol on the incorrect label has a white background instead of yellow, and the label is missing the high voltage warning symbol. This presents a potential risk of electrical shock for service personnel.

Status: Ongoing

Product Quantity: 7 US; 16 ROW total

Code Information:

Model No. 781260 UDI-DI 00884838095076 Serial Numbers 21020 9024 8657 21200 21223 18948 32131; Model No. 782112 UDI-DI 00884838098886 Serial Numbers 30089 20204

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AR, CO, IL, MD, MS, NE, TX and the countries of Brazil, Canada, China, Germany, Greece, India, Mexico, and Saudi Arabia.

Voluntary or Mandated:

Voluntary: Firm initiated