Reported Jun 26, 2013 · Terminated

Philips BuckyDiagnost Radiographic, a Diagnostic X-ray system. Catalog Numbers: 704031, 704032, 704035, 704060, 704062…

Philips Healthcare Inc.

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 Healthcare Inc. · 3000 Minuteman Road · Andover, MA · 01810

Is this the product you have?

  • Philips BuckyDiagnost Radiographic, a Diagnostic X-ray system
  • Catalog Numbers704031, 704032, 704035, 704060, 704062 This system is used for making x-ray exposures for diagnostics
Lot codes and dates
  • Serial Numbers

    64 of 64 codes

    • 335292
    • 351085
    • 351326
    • 348891
    • 348895
    • 353313
    • 358016
    • 359426
    • 370503
    • 354382
    • 354749
    • 369640
    • 380748
    • 356820
    • 362256
    • 357699
    • 362257
    • 357255
    • 358489
    • 380361
    • 363543
    • 362719
    • 363669
    • 363544
    • 363305
    • 363538
    • 365150
    • 364211
    • 379698
    • 380749
    • 375725
    • 375727
    • 375729
    • 377144
    • 381880
    • 381881
    • 380798/SN07000617
    • 381877
    • 383767/SN07000639
    • 392883/SN08000099
    • 394519/SN08000135
    • 421035/SN09000031
    • 396577/SN08000190
    • 402575/SN08000382
    • 397513/SN08000185
    • 407681/SN08000345
    • 411751/SN08000438
    • 410786/SN08000454
    • 417251/SN08000547
    • 427833/SN09000208
    • 415998/SN08000511
    • 416000/SN08000508
    • 421979/SN09000098
    • 422100/SN09000216
    • 442036/SN09000336
    • 448226/SN09000416
    • 455130/SN10000286
    • 462191/SN10000266
    • 468071/SN10000398
    • 467831/SN10000326
Amount recalled
66 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

Why it was recalled

An inspection shows several IATDs (Installation Acceptance Test could not be located or different templates have been used

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

Notice updated Oct 15, 2013 · Data as of Sep 19, 6:52 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.