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All product recalls associated with Plus Orthopedics USA.
Total Recalls
21
Past Year
0
Class I (Serious)
0
Most Recent
Nov 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.
The VKS "Tibial Trial" was found to have an incorrect fixation pin hole diameter.
Labeling Error: The VKS PE Ultra-congruent insert package, may actually contain a Standard PE insert.
The modified devices were distributed by Plus Orthopedics USA (Plus USA) June 10, 2003 prior to FDA approval to market of the modified device (Special 510(k) K032052, clearance date July 25, 2003) and withdrawn from the field June 25, 2003.