Home/Recalls/FDA-Z-1214-2026
FDA DevicesClass II

Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R...

Published: February 4, 2026Recall ID: Z-1214-2026Category: devicesCountry: US

Reason for Recall / Hazard

The potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).

Product Description & Identification

Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R11.1 and R12.1.

Affected Products

Upgrade to MR 7700. Product Code (REF): 782130. MR systems with SW version R11.1 and R12.1.

Additional Source Details

FieldValue
CityCambridge
StateMA
Event id98111
Address 1222 Jacobs St
Address 2N/A
Code infoMR systems with SW version R11.1 and R12.1. Product Code (REF): 782130. UDI-DI: 00884838104402. Serial Numbers: 42030, 85644, 42163, 42151, 45236, 85643.
Postal code02141-2296
Report date20260204
Product typeDevices
Product quantity6 units
Reason for recallThe potential for stiffness value errors when viewing exported MR Elastography (MRE) stiffness maps to viewer Picture Archiving and Communication System (PACS).
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20251203
Initial firm notificationLetter
Center classification date20260129

Overview

  • Recalling FirmPhilips North America
  • StatusOngoing
  • Risk LevelClass II
  • DistributionWorldwide - US Nationwide distribution in the states of AZ, CA, CO, IL, MA, ME, MI, MN, MS, NE, NY, OH, OR, PA, SC, TN, TX, VA, VT, WA and the countries of Belgium, Canada, Denmark, France, Germany, Greece, India, Israel, Japan, Kenya, Netherlands, South Korea, Spain, Sweden, Taiwan, Thailand, United Kingdom.
Official Agency Alert