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Recall Observatory FDA recall evidence

Device product

Combiset Blood Line with BVM for Hemodialysis use Catalog Number: 03-2965-9. Intended for use as the extracorporeal blood circuit during Hemodialysis and is indicated for use with conventional and high flux negative pressure hemodialyzer equipment.

Z-0185-2014

August 29, 2013

Class II

Product summary

Firm
Fresenius Medical Care Holdings, Inc.
Event
Event 65739
Status
Terminated
Classification
Class II
Quantity
24,202 cases
Official record key
device-enforcement:Z-0185-2014

Official wording

Reason: Updated Instructions for Use: Bloodline connections not tightened per instructions in the operator's manual may disconnect and lead to blood loss

Code information: All lot codes

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

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Updated Instructions for Use: Bloodline connections not tightened per instructions in the operator's manual may disconnect and lead to blood loss