Medical Device Recall: COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.
DePuy Mitek, Inc., a Johnson & Johnson Co. · February 24, 2025
Reason for Recall
Device is missing the pin in the graft loader component.
Distribution
Domestic: Nationwide Distribution; Foreign: Austria, Belgium, Brazil, Switzerland, Chile, China, Colombia, Czech Republic, Germany, Spain, Finland, France, French Guyana, Greece, Israel, India, Italy, Japan, South Korea, Luxemburg, Mexico, Netherlands, Poland, Portugal & Singapore.
States Affected
NATIONWIDE
Quantity Affected
US: 131 units; OUS: 312 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1315-2025
Status: ongoing
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