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Recall Observatory FDA recall evidence

Device product

UniCel DxC 600i SYNCHRON Access Clinical Systems; A25656, A25638. In vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids.

Z-0310-2018

November 06, 2017

Class III

Product summary

Firm
Beckman Coulter Inc.
Event
Event 78613
Status
Terminated
Classification
Class III
Quantity
2 units
Official record key
device-enforcement:Z-0310-2018

Official wording

Reason: Potential for minor skin burn if the tool contacts the reagent storage interface board (B79917) when performing a pipettor alignment.

Code information: Serial/Lot Numbers: 801060 and 801061

Distribution pattern: Worldwide Distribution -- US, Argentina, Canada, Chile, China, Columbia, Costa Rica, France, Georgia, Germany, Ghana, Greece, Hong Kong, India, Italy, Japan, Kazakhstan, Mexico, Morocco, Myanmar, Nepal, Philippines, Poland, Russia, Rwanda, Saudi Arabia, Slovakia, South Africa, South Korea, Thailand, Turkey, United Kingdom, and Vietnam.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential for minor skin burn if the tool contacts the reagent storage interface board (B79917) when performing a pipettor alignment.