Reported May 22, 2024 · Ongoing

Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.

Philips North America LLC

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 Llc · 222 Jacobs St · Cambridge, MA · 02141-2289

Is this the product you have?

  • Patient Information Center iX and Patient Information Center iX Expand, Software Version 4.x.
Lot codes and dates
  • Model No. 866389 and 866390
  • UDI-DI

    242 of 242 codes

    • n/a
    • Serial No. 7G6G-7PGV-W
    • 5971-2NL7-Z
    • 6D62-19MD-9
    • 463N-67ME-X
    • 6U1W-7TJA-9
    • 5K2A-6DHP-K
    • 5E42-35J4-P
    • 4E6Z-70HU-B
    • 1T12-0MNA-C
    • 0C0L-0FKE-4
    • 2H34-3MMP-U
    • 6P1E-7HJU-W
    • 3R6X-3XNY-6
    • 7F50-53NK-L
    • 3Z3B-1AHM-H
    • 0128-2WG5-0
    • 0K6E-39G4-5
    • 0C5Y-7FHX-V
    • 0X7R-2AGC-Y
    • 0P5D-5VMH-V
    • 2K0X-0TLA-F
    • 6627-6MKH-U
    • 5J7B-1XPT-T
    • 7U4C-44NB-E
    • 2Y7R-5KGZ-W
    • 1P22-0XNW-P
    • 1004-6RJX-E
    • 1U0P-0FKE-C
    • 396T-5ZH1-5
    • 0Y0Z-3GJ0-A
    • 7Y5Z-7FHX-F
    • 7U76-1HM0-D
    • 2X44-7ELE-J
    • 7Z3Y-0LJ3-2
    • 7R7A-6CPV-0
    • 3C44-7ELE-4
    • 2L0L-0FKE-A
    • 1V70-3XNY-9
    • 5A4T-57JE-R
    • 375F-7UMF-K
    • 6031-24GX-X
    • 2M2G-15LB-E
    • 2630-65P4-3
    • 6E64-7XLV-M
    • 3K33-61K2-0
    • 227N-7JG6-J
    • 6X1X-3CH6-V
    • 0T41-35J4-A
    • 4R0G-60JV-1
    • 414L-03P1-E
    • 6Y4B-44NB-J
    • 7C5C-7UMF-D
    • 1305-0UH7-M
    • 116V-21KC-Z
    • 4R1J-18LJ-4
    • 3A0H-6AMX-6
    • 4R03-1FHE-U
    • 5C4L-7WMK-2
    • 6B35-3MMP-T
Amount recalled
358 units (US: 45; OUS: 313)

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Event Catalog information does not save when copied and transferred from one unit to another.

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, 6:17 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.