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Recall Observatory FDA recall evidence

Derived label

Device software or design

Por fullct fem st 15x200mm, Sterile, prosthesis, hip, semi-constrained, metal/polymer, porous uncemented- Specific Knee, Hip and Nail Implants

reason.device_software_design

v1.0.0

Assignment summary

Mode key
device_software_design
Evidence excerpt
design verification test failures
Rule explanation
Device recall wording explicitly identifies a software, firmware, programming, cybersecurity, or design defect and its failure or consequence.
Firm
Zimmer Biomet, Inc.

Field note

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