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Recall Observatory FDA recall evidence

Device product

CS 8100 3D, CATALOG # (s): 5311162, 5311188. Intended to produce complete or segmented tomographic digital panoramic X-ray images and three-dimensional digital X-ray images of the dentomaxillo-facial area to be used at the direction of healthcare professionals as diagnostic support for pediatric and adult patient.

Z-1378-2015

January 08, 2015

Class II

Product summary

Firm
Carestream Health, Inc.
Event
Event 70649
Status
Terminated
Classification
Class II
Quantity
470 units (127 domestically & 343 internationally)
Official record key
device-enforcement:Z-1378-2015

Official wording

Reason: Units device head descended unexpectedly

Code information: All serial numbers of affected devices.

Distribution pattern: Worldwide Distribution -- US, including the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NV, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, VT, WA, WI, and WV; and the countries of India and Switzerland.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Units device head descended unexpectedly