Philips North America: Medical Device Recall in 2024 - (Recall #: Z-0732-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

(1) CareEvent, Model No. 866435 (2) CareEvent Upgrade, Model no. 866436

Product Classification:

Class II

Date Initiated: November 28, 2023

Date Posted: January 24, 2024

Recall Number: Z-0732-2024

Event ID: 93638

Reason for Recall:

Push notifications may fail to send to the user under certain conditions. This could potentially result in patient harm due to delay in detection of a change in patient condition.

Status: Ongoing

Product Quantity: 254 US; 37 OUS

Code Information:

UDI-DI: 00884838099128 Software: CareEvent Version C.03.X

Distribution Pattern:

Worldwide distribution: US (Nationwide) to states of: CA, GA, IA, MA, MI, MN, NJ, NM, NY, OH, PA, TN, TX, WA, WV; and OUS (Foreign) distribution to countries of: Australia, Austria, Belarus, Belgium, Brazil, Canada, Czech Republic, Denmark, Estonia, Faroe Islands, Finland, France, Germany, India, Indonesia, Ireland, Italy, Japan, Lithuania, Luxembourg, Mexico, Netherlands, New Zealand, Norway, Oman, Philippines, Poland, Romania, Saudi Arabia, Singapore, Slovakia, South Africa, South Korea, Spain, Sweden, Switzerland, Thailand, United Kingdom, Utd.Arab.Emir., and Uzbekistan

Voluntary or Mandated:

Voluntary: Firm initiated