Reported Jul 10, 2019 · Terminated

Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System Model Number: 10848282

Siemens Medical Solutions USA, 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: Siemens Medical Solutions USA, Inc · 40 Liberty Blvd · Malvern, PA · 19355-1418

Is this the product you have?

  • Siemens Artis Q biplane---Interventional
  • Fluoroscopic X-Ray System Model Number10848282
Lot codes and dates
  • Serial Numbers

    72 of 72 codes

    • 121013
    • 121057
    • 121056
    • 121058
    • 121006
    • 121185
    • 121016
    • 121027
    • 121020
    • 121321
    • 121448
    • 121040
    • 121049
    • 121015
    • 121094
    • 121082
    • 121089
    • 121383
    • 121144
    • 121319
    • 121137
    • 121085
    • 121155
    • 121193
    • 121136
    • 121165
    • 121140
    • 121141
    • 121151
    • 121168
    • 121169
    • 121154
    • 121211
    • 121188
    • 121415
    • 121183
    • 121209
    • 121187
    • 121309
    • 121200
    • 121313
    • 121206
    • 121361
    • 121366
    • 121359
    • 121393
    • 121301
    • 121407
    • 121406
    • 121352
    • 121379
    • 121364
    • 121342
    • 121471
    • 121520
    • 121411
    • 121412
    • 121402
    • 121430
    • 121502
Amount recalled
73

This recall covers 20 products

The agency filed one notice per product. You are reading one of them; the other 19 are below.

7 more are in the archive.

Where it was sold

  • Nationwide

Why it was recalled

Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel

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.

Free recall alerts

Get alerted about new Siemens Medical Solutions USA, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Feb 9, 2021 · 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.