Reported Mar 12, 2014 · Terminated

Model Kodak 2200 Intraoral X-Ray System, Catalog Numbers 5303177, 5303169, 5303151, XR-5154323 -- Carestream Health,…

Carestream Health 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: Carestream Health Inc. · 150 Verona St · Rochester, NY · 14608-1733

Is this the product you have?

    • Model Kodak 2200 Intraoral X-Ray System
    • Catalog Numbers 5303177
    • 5303169
    • 5303151
    • XR-5154323 -- Carestream Health
    • Inc
  • Made in France -- --- COMMON/USUAL NAMEDental
  • X-Ray Systems -- CLASSIFICATION NAMEUnit, X-Ray, Extraoral with timer ---
  • There are four major componentsx-ray tube, x-ray generator, collimator and image receptor. These systems are permanently installed diagnostic dental x-ray systems for generation of x-rays for examination of the teeth, jaw and oral structures
Lot codes and dates
  • Serial Numbers starting with WE, WF, WG, WH, WI, WJ, WK, WL, XA, XB, XC, XD, XE, XF, XG, XH, XI, XJ, XK, XL, YA, YB, YC, YD
Amount recalled
Domestic: 347 units (total for both)

This recall covers 2 products

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

Where it was sold

  • Nationwide

Why it was recalled

Carestream received problem reports relating to apparent early failure of Kodak 2X00 Intraoral X-ray device arms leading to arm breakage.

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 Jun 18, 2015 · Data as of Sep 19, 5:31 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.