Philips North America Llc: Medical Device Recall in 2022 - (Recall #: Z-0460-2023)

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 Ingenia Elition X MR System, Model Numbers 781358, 782107, 782119, 782136

Product Classification:

Class II

Date Initiated: November 22, 2022

Date Posted: December 14, 2022

Recall Number: Z-0460-2023

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: 566 total

Code Information:

Model 781358: UDI-DI: 00884838088115; Serial Numbers: 45002 45051 45075 45108 45133 45164 45243 45269 45337 45356 45010 45053 45086 45112 45147 45178 45245 45296 45338 45357 45011 45054 45087 45113 45150 45179 45247 45321 45343 45364 45024 45060 45089 45124 45152 45194 45252 45322 45353 45395 45027 45068 45099 45132 45161 45238 45263 45335 45355 45414 45026 45055 45082 45100 45235 45237 45264 45315 45398 45423 45032 45078 45092 45146 45236 45261 45277 45316 45399 45429 45035; Model Number 782107: UDI-DI: 00884838098336; Serial Numbers: 45563 45570; Model Number 782119: UDI-DI: 00884838104129; Serial Numbers: Included in Letter but No Devices Distributed in US Model Number 782136: UDI-DI: 00884838108608; Serial Numbers: Included in Letter but No Devices Distributed in US

Distribution Pattern:

US Nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated