Philips North America Llc: Medical Device Recall in 2022 - (Recall #: Z-0463-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Philips Upgrade to MR 7700 System, Model Number 782130

Product Classification:

Class II

Date Initiated: November 22, 2022

Date Posted: December 14, 2022

Recall Number: Z-0463-2023

Event ID: 91195

Reason for Recall:

Gradient Coil may act as a heat source with a potential to produce smoke and/or fire.

Status: Ongoing

Product Quantity: N/A

Code Information:

Model 782120: UDI-DI: 00884838104402; Serial Numbers: 45298 45301

Distribution Pattern:

US Nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated