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All product recalls associated with Medstone International Inc.
Total Recalls
2
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2004
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.
Units are defective in that the identification and certification labels were inadequate or missing. The beam limiting device was not appropriate for general purpose radiographic procedures and the beam limiting device could ot collimate down to 125 square centimeters or less as required.
X-ray tube arm and collimator fell and fractured patient's ribs.