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Recall Observatory FDA recall evidence

Device product

INTRABEAM Balloon Applicator Set; 4.0 cm, Carl Zeiss Meditec AG, Oberkochen, Germany INTRABEAM System is intended for radiation therapy treatments.

Z-0406-2013

October 25, 2012

Class II

Product summary

Firm
Carl Zeiss Meditec, Inc.
Event
Event 63596
Status
Terminated
Classification
Class II
Quantity
36 total, all lots
Official record key
device-enforcement:Z-0406-2013

Official wording

Reason: A manufacturing defect has been identified which could results in the small tube becoming dislodged between the luer fitting and the check valve.

Code information: Part number 304534-7500-002; lot number 540960.

Distribution pattern: Nationwide Distribution including IL and MD

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    manufacturing defect