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Recall Observatory FDA recall evidence

Device product

PrepStain Tecan US-I. For use in the screening and detection of cervical cancer.

Z-2111-2013

July 08, 2013

Class II

Product summary

Firm
Becton Dickinson & Co.
Event
Event 65779
Status
Terminated
Classification
Class II
Quantity
890 instruments
Official record key
device-enforcement:Z-2111-2013

Official wording

Reason: PrepStain system rack setting was incorrectly entered on one PrepStain system during a routine preventive maintenance visit by a BD Field Service Representative.

Code information: Catalog Numbers - 799-13000-00 and 799-13000-00R

Distribution pattern: Worldwide Distribution-USA (nationwide) and Puerto Rico and the country of Canada.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    PrepStain system rack setting was incorrectly entered on one PrepStain system during a routine preventive maintenance visit by a BD Field Service Representative.