Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DePuy Mitek Tissue Liberator -Blade Up Catalog Number: 214623 The Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co. Due to Labeled incorrectly as a Blade Up configuration instead...
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 DePuy Mitek, Inc., a Johnson & Johnson Co. directly.
Affected Products
DePuy Mitek Tissue Liberator -Blade Up Catalog Number: 214623 The Reusable Arthroscopy Instruments are reusable, non-powered surgical instruments used during arthroscopic surgery of any joint except the spine.
Quantity: 27 units
Why Was This Recalled?
Labeled incorrectly as a Blade Up configuration instead of a Blade Down configuration.
Where Was This Sold?
This product was distributed to 2 states: KY, NJ
About DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek, Inc., a Johnson & Johnson Co. has 51 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report