Reported Apr 3, 2024 · Ongoing

CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X

Philips North America

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Philips North America · 222 Jacobs St · Cambridge, MA · 02141-2296

Is this the product you have?

  • CareEvent Event Management System, Model Numbers 866435 and 866436 (CareEvent Upgrade), Software Version Number C.03.X
Lot codes and dates
  • UDI-DI(01)00884838099128(10)C.03.00
  • Serial Numbers

    541 of 541 codes

    • 5T6W-21KC-4
    • 3L0R-7AHH-C
    • 1F1G-01JC-6
    • 415A-26K6-9
    • 605K-5AGH-2
    • 5J5G-0ZNF-4
    • 7A6D-4TL3-Y
    • 233Z-0LJ3-C
    • 142W-3VM1-3
    • 1863-19MD-E
    • 3F0T-7AHH-C
    • 4R5K-5AGH-W
    • 2T5M-55J9-W
    • 0U6Z-70HU-B
    • 795Z-7FHX-E
    • 2K3W-3PJ8-0
    • 3T5Z-7FHX-2
    • 0B13-0MNA-8
    • 0R0E-63JK-C
    • 644J-1CJJ-1
    • 470D-63JK-A
    • 2022-0XNW-V
    • 5W2A-5MGJ-D
    • 0141-2RHR-B
    • 6944-5RM5-A
    • 7G7Y-76MW-C
    • 0L09-3WPK-J
    • 2R1E-50P2-3
    • 3967-33KR-R
    • 3H3M-28MC-X
    • 4E1V-5LH0-8
    • 5Y57-68PX-9
    • 150B-02P6-L
    • 3W5D-7UMF-J
    • 0C33-3MMP-U
    • 181U-7TJA-2
    • 2V6Z-1ZL8-C
    • 2468-33KR-T
    • 0J1J-1KG1-4
    • 591H-1KG1-9
    • 194W-72P0-E
    • 2Y57-6TKK-D
    • 2W0U-6WNX-P
    • 7L3W-3PJ8-R
    • 2044-77KZ-8
    • 2G1U-7TJA-9
    • 6E7C-1XPT-M
    • 7L0M-4AH2-1
    • 0U41-6BK3-L
    • 6G5N-4LGG-3
    • 232E-2FMY-X
    • 6R22-07LZ-R
    • 1P5K-5AGH-2
    • 2378-6CPV-2
    • 0550-53NK-T
    • 0F13-59N8-K
    • 1M4Y-78J7-0
    • 0B5Z-7FHX-F
    • 4C04-4ZPR-E
    • 0V6H-7PGV-K
Amount recalled
2,323 Units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Where it was sold

  • Nationwide

Why it was recalled

It was found that the Care Assist mobile application (version 4.1.1 and earlier) would not play custom ringtones when iOS device screens were locked with a passcode.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.