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Recall Observatory FDA recall evidence

Derived label

Device software or design

ProGuide Chronic Dialysis Catheters, REF: DC01455550/C, DC21452419/C, DC21452419-NE5/C, DC21452823-NE5/C, DC21454035/C, DC21455550/C

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
design defect
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
Merit Medical Systems, Inc.

Field note

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