Reported Aug 29, 2018 · Terminated

DigitalDiagnost Dual Detector (Stitching Patient Support) 712022

Philips Medical Systems GmbH, DMC

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 Medical Systems Gmbh, DMC · Development And Manufacturing Ctr. · Hamburg · N/A

Is this the product you have?

  • DigitalDiagnost Dual Detector (Stitching Patient Support) 712022
Lot codes and dates
  • Serial Numbers

    78 of 78 codes

    • 488713/SN11000577
    • 488714/SN11000572
    • 444623/SN10000136
    • 480503/SN11000473
    • 480504/SN11000478
    • 410040/SN08000021
    • 422832/SN09000061
    • 462407/SN10000363
    • 448130/SN10000008
    • 464981/SN10000471
    • 455752/SN10000200
    • 454061/SN10000216
    • 426292/SN09000386
    • 455546/SN10000143
    • 420090/SN09000018
    • 474817/SN11000080
    • 474238/SN11000042
    • 461799/SN10000347
    • 455621/SN10000163
    • 471148/SN11000122
    • 471147/SN11000120
    • 482904/SN11000375
    • 482905/SN11000373
    • 482903/SN11000379
    • 440249/SN09000347
    • 481021/SN11000446
    • 487808/SN11000526
    • 441778/SN09000452
    • 432989/SN09000285
    • 478307/SN12000004
    • 476338/SN12000026
    • 476034/SN12000027
    • 422536/SN09000199
    • 486638/SN11000494
    • 466808/SN10000464
    • 462593/SN10000439
    • 471150/SN10000660
    • 478233/SN11000233
    • 473897/SN11000165
    • 482501/SN11000527
    • 453200/SN10000133
    • 456093/SN10000204
    • 461979/SN10000701
    • 461976/SN10000704
    • 443093/SN09000454
    • 445110/SN09000461
    • 16750755
    • 477524/SN11000434
    • 475932/SN11000341
    • 475866/SN11000350
    • 451542/SN10000098
    • 442534/SN09000423
    • 443443/SN09000420
    • 484558/SN11000525
    • 479928/SN11000287
    • 466029/SN10000420
    • 472613/SN11000162
    • 480061/SN11000474
    • 453085/SN10000125
    • 467927/SN10000713
    ***Added 5/6/21*** SN15000449

This recall covers 28 products

The agency filed one notice per product. You are reading one of them; the other 27 are below.

15 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

The hook does not securely hold the footplate in the vertical position. Therefore, the footplate can fall or swing down and injury operator or patient.

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

Notice updated Apr 30, 2024 · Data as of Sep 19, 4:47 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.