Invivo Corporation: Medical Device Recall in 2014 - (Recall #: Z-0069-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Philips Expression MR200 MRI Patient Monitoring System

Product Classification:

Class II

Date Initiated: September 5, 2014

Date Posted: October 22, 2014

Recall Number: Z-0069-2015

Event ID: 69179

Reason for Recall:

Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.

Status: Terminated

Product Quantity: 24 units.

Code Information:

Model: 866120, Lot numbers: US33600004, US33600005, US33600006, US33600007, US33600008, US33600009, US33600010, US33600011, US33600012, US33600013, US33600014, US33600015, US33600016, US33600017, US33600018, US33600019, US33600020, US33600022, US33600023, US33600024, US33600025, US33600026, US33600027, US33600028.

Distribution Pattern:

Worldwide Distribution - US including the states of CA, GA, MI, NJ, NV, and TX., and the countries of: Austria, Finland, Germany, Poland, Singapore, Sweden, Switzerland and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated