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Recall Observatory FDA recall evidence

Device product

Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is indicated for radiation therapy treatments

Z-0001-2018

August 30, 2017

Class II

Product summary

Firm
Carl Zeiss Meditec AG
Event
Event 78082
Status
Terminated
Classification
Class II
Quantity
9 devices
Official record key
device-enforcement:Z-0001-2018

Official wording

Reason: The device had an incorrect printed calibration value on the calibration certificate.

Code information: Intrabeam ser. #6402501246, Ion chamber ser. #SN001254; Intrabeam ser. #6402501241, Ion chamber ser. #SN001745; Intrabeam ser. #6402100932, Ion chamber ser. #SN001994; Intrabeam ser. #6402100958, Ion chamber ser. #SN002096; Intrabeam ser. #6402101042, Ion chamber ser. #SN002265; Intrabeam ser. #6402101029, Ion chamber ser. #SN002270; Intrabeam ser. #6402101034, Ion chamber ser. #SN002302; Intrabeam ser. #6402101105, Ion chamber ser. #SN002651; and Intrabeam ser. #6402101130, Ion chamber ser. #SN002684.

Distribution pattern: Nationwide Distribution including AZ, CA, CT, DC, FL, GA, OH, and PA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The device had an incorrect printed calibration value on the calibration certificate.