Reported Apr 19, 2023 · Ongoing

Philips DigitalDiagnost C50 -intended for use in generating radiographic images of human anatomy Model Number : 712201

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?

  • Philips DigitalDiagnost C50 -intended for use in generating radiographic
  • images of human anatomy Model Number712201
Lot codes and dates
  • UDI-DI(01)00884838082366(21)
  • USSerial
  • Numbers200072 200131 200132 200143 SN170053 SN180074
  • SN180163 SN180181 SN180182 SN190119 OUS

    574 of 574 codes

    • 200004
    • 200005
    • 200006
    • 200011
    • 200014
    • 200015
    • 200031
    • 200039
    • 200040
    • 200041
    • 200043
    • 200046
    • 200047
    • 200048
    • 200050
    • 200054
    • 200058
    • 200059
    • 200060
    • 200061
    • 200062
    • 200063
    • 200064
    • 200065
    • 200067
    • 200068
    • 200069
    • 200070
    • 200072
    • 200073
    • 200074
    • 200075
    • 200077
    • 200078
    • 200079
    • 200080
    • 200081
    • 200082
    • 200083
    • 200085
    • 200087
    • 200089
    • 200090
    • 200091
    • 200092
    • 200093
    • 200095
    • 200096
    • 200098
    • 200099
    • 200100
    • 200101
    • 200102
    • 200103
    • 200104
    • 200105
    • 200106
    • 200107
    • 200108
    • 200109
Amount recalled
US: 10 units; OUS: 570 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

If the PM for the telescopic carriage is not performed annually as defined in the Instructions for Use (IFU), the tension force of the spring balancer inside of the telescopic carriage will unavoidably decay through normal wear and tear; as a result there is a potential that the Ceiling Suspension of the DigitalDiagnost C50 system may descend inadvertently if power to the system is interrupted, and may result in injuries to patients and users

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

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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, 7:35 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.