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All product recalls associated with Laborie Medical Technologies.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
Most Recent
Jan 2026
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.
Mislabeling: Product labeled with incorrect "Use Before" date and pouch labels missing lot number. (Incorrect dates-2006/07 or 2006/08; correct Use by dates-2009/08 for Lot 36H03M005 and 2009/07 for Lot 36G20M041
Component assembly; The fill chuck is not assembled properly which may allow the device to come apart over time releasing its contents.
Device Fracturing: recent design and process changes leave the device susceptible to fracturing, which could cause the prosthesis to fail