Skip to content
Recall Observatory FDA recall evidence

Device product

IntelliVue MX40 Patient Monitor, Software Versions B.05, B.06, B.06.5X, Model 865351

Z-2142-2018

April 30, 2018

Class II

Product summary

Firm
Philips Electronics North America Corporation
Event
Event 80064
Status
Terminated
Classification
Class II
Quantity
7,178
Official record key
device-enforcement:Z-2142-2018

Official wording

Reason: Five warning statements are missing from the instructions for use.

Code information: All devices since release of B.05 (March 2016) prefix date code >/= US096

Distribution pattern: Worldwide Distribution -- US, to the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, and to the territories of Guam and Puerto Rico; and, countries of Argentina, Australia, Austria, Belgium, Canada, Chile, China, Croatia, Czech Republic, Denmark, Estonia, Finland, France, German, Ghana, Greece, Guadeloupe, Hong Kong, Iceland, India, Ireland, Israel, Italy, Japan, Latvia, Lebanon, Malaysia, Martinique, Mexico, Myanmar, Netherlands, New Zealand, Norway, Philippines, Poland, Portugal, Qatar, Russia, Saudi Arabia, Singapore, Slovenia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, UK, UAE, and Vietnam.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Five warning statements are missing from the instructions for use.