Invivo Corporation: Medical Device Recall in 2015 - (Recall #: Z-0958-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Philips Expression MR200 MRI Patient Monitoring System.

Product Classification:

Class II

Date Initiated: October 22, 2014

Date Posted: January 21, 2015

Recall Number: Z-0958-2015

Event ID: 69587

Reason for Recall:

The MR 200 devices failed the initial power up test due to capacitor short and hi-pot testing; possible loss of Patient Monitoring or User/Service Electrical Shock.

Status: Terminated

Product Quantity: 20

Code Information:

Model No. 866120; Lot/ Serial Numbers: US33600065, US33600066, US33600075, US33600077, US33600078, US33600079; US33600080, US33600081, US33600082, US33600083, US33600084, US33600086, US33600087, US33600088, US33600089, US33600090, US33600091, US33600092, US33600093, US33600094.

Distribution Pattern:

CA, FL, IN, KY, MN, NC, NJ, NY, OK, SD and TX Netherlands, Poland and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated