Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
***REF C7120***APEX Arthroscopy Tubing Set. Intended for use for joint Recalled by Linvatec Corp. dba ConMed Linvatec Due to Conmed Linvatec received complaints that their products C7120...
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
***REF C7120***APEX Arthroscopy Tubing Set. Intended for use for joint irrigation and dissention during arthroscopic procedures.
Quantity: 4,691 Units total of each
Why Was This Recalled?
Conmed Linvatec received complaints that their products C7120 APEX Arthroscopy Tubing Set, One Connection and C7122 APEX Arthroscopy Tubing Set, Two Connection, contained a scratch/grooved area on the inside diameter of the pressure fitting that may cause the APEX Irrigation (pump) Console to sense a pressure drop and increase fluid flow to the surgical site.
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