Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec Due to The Membrane Switch Panel (referred to as "front...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Linvatec Corp. dba ConMed Linvatec directly.
Affected Products
D3000I Advantage Drive System, 230v, surgical instrument motor. Product Usage: The Advantage Drive Systems function as a powered instrument system consisting of handpieces and accessories to perform cutting of soft tissue and bone
Quantity: 23 units
Why Was This Recalled?
The Membrane Switch Panel (referred to as "front panel" of the component part number A34-003-207, used on both the D3000 and D3000I Advantage Drive System, contained the incorrect symbology per third edition IEC60606-01 Medical Electrical Equipment: General requirements for basic safety and essential performance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Linvatec Corp. dba ConMed Linvatec
Linvatec Corp. dba ConMed Linvatec has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report