Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
TOPAZ MicroDebrider 0.8 mm REF AC4040-01 Recalled by ArthroCare Corporation Due to During functional testing of devices after real time...
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 ArthroCare Corporation directly.
Affected Products
TOPAZ MicroDebrider 0.8 mm REF AC4040-01; TOPAZ MicroDebrider IFS 0.8 mm REF ACH4040-01; TOPAZ MicroDebrider 0.8 mm REF Q6000-01; TOPAZ EPF MicroDebrider 0.8 mm 45 REF Q6002-01
Quantity: 26,903 devices
Why Was This Recalled?
During functional testing of devices after real time aging, it was determined that product failed to meet shelf-life at the expiration date indicated on the product labels.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ArthroCare Corporation
ArthroCare Corporation has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report