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DePuy Mitek, Inc., a Johnson & Johnson Co. recalls DePuy Mitek Tissue Liberator -Blade Up Catalog Number: 214623 The Reusable Arthroscopy Instruments are reusable, no
Recalled May 15, 2013 · FDA recall Z-1278-2013 · DePuy Mitek, Inc., a Johnson & Johnson
Hazard
Labeled incorrectly as a Blade Up configuration instead of a Blade Down configuration. · FDA Class II
Units
27 units
Sold at
Worldwide Distribution - USA including KY, NJ and Internationally to Argnetina, Australia, Belgium,Columbia, India, France, Japan, Jordan, Latvija, Israel, Korea, and Great Britain. For questions regarding this recall call 508-977-3813.
Description
Labeled incorrectly as a Blade Up configuration instead of a Blade Down configuration.
Product
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.
Manufacturer(s)
DePuy Mitek, Inc., a Johnson & Johnson Co.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →