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All product recalls associated with CLINICAL LASERTHERMIA SYSTEMS AB Scheelevagen.
Total Recalls
1000
Past Year
423
Class I (Serious)
54
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.
single use devices labeled as sterile may not have been adequately sterilized
Failed Stability Specifications: product did not meet viscosity results.
Flags edited in RayCare after a patient has been checked in may not always be updated in RayTreat.