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All product recalls associated with Kinetic Concepts, Inc.
Total Recalls
10
Past Year
0
Class I (Serious)
0
Most Recent
Mar 2006
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Complaints received regarding difficulty opening the nonadherent layer of the device prior to application to open abdominal wounds.
Possible mislabeling of shipping cartons.
To correct software issues in software versions 1.3 and 1.5 and to upgrade hatch latch handles to a more ergonomic design.