Reported Nov 15, 2023 · Ongoing

CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system

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?

  • CombiDiagnost R90, Radiography and Fluoroscopy (R/F) system
Lot codes and dates
  • Model No. 709030 and 709031
  • UDI

    92 of 92 codes

    • (01)00884838076747(21) SN17000014
    • (01)00884838076747(21) 10000020
    • (01)00884838076747(21) SN17000130
    • (01)00884838076747(21) SN17000123
    • (01)00884838076747(21) SN18000021
    • (01)00884838076747(21) SN18000001
    • (01)00884838076747(21) SN18000075
    • (01)00884838076747(21) SN18000002
    • (01)00884838076747(21) 10000004
    • (01)00884838076747(21) SN17000144
    • (01)00884838076747(21) SN17000140
    • (01)00884838076747(21) SN18000003
    • (01)00884838076747(21) SN18000063
    • (01)00884838076747(21) SN18000018
    • (01)00884838076747(21) SN18000022
    • (01)00884838076747(21) SN18000041
    • (01)00884838076747(21) SN18000031
    • (01)00884838076747(21) 10001097
    • (01)00884838076747(21) 10000056
    • (01)00884838076747(21) 28
    • (01)00884838076747(21) 10000184
    • (01)00884838076747(21) SN19000018
    • (01)00884838076747(21) SN19000006
    • (01)00884838076747(21) SN19000040
    • (01)00884838076747(21) SN19000001
    • (01)00884838076747(21) SN19000041
    • (01)00884838076747(21) 10000051
    • (01)00884838076747(21) 10000000
    • (01)00884838076747(21) 10000087
    • (01)00884838076747(21) 10001095
    • (01)00884838076747(21) 10000122
    • (01)00884838076747(21) 10001001
    • (01)00884838076747(21) 10000145
    • (01)00884838076747(21) 10000152
    • (01)00884838076747(21) 10000190
    • (01)00884838076747(21) 10001076
    • (01)00884838076747(21) SN17000153
    • (01)00884838101456(21) 10001054
    • (01)00884838101456(21) 10001087
    • (01)00884838101456(21) 10001086
    • (01)00884838101456(21) 10001159
    • (01)00884838101456(21) 10001109
    • (01)00884838101456(21) 10001114
    • (01)00884838101456(21) 10001171
    • (01)00884838101456(21) 10001194
    • (01)00884838101456(21) 10001193
    • Serial No. SN17000014
    • 10000020
    • SN17000130
    • SN17000123
    • SN18000021
    • SN18000001
    • SN18000075
    • SN18000002
    • 10000004
    • SN17000144
    • SN17000140
    • SN18000003
    • SN18000063
    • SN18000018
Amount recalled
46 units

This recall covers 10 products

The agency filed one notice per product. You are reading one of them; the other 9 are below.

Where it was sold

  • Nationwide

Why it was recalled

Potential for units suspended on the ceiling to fail and fall.

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.