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All product recalls associated with Philips Medical Systems North America Co. Phillips.
Total Recalls
1000
Past Year
353
Class I (Serious)
22
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.
Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.
Advanced Sterilization Products (ASP) has discovered a defect in the barcode labeling of the STERRAD NX System Cassettes 10133, Lot #08I032. This is the only lot number affected by this action. The barcodes for Lot #08I032 were printed improperly and are not capable of being read by the STERRAD unit.
Tube failure occurs involving fluoroscopy of large patients and a partial failure of the grid switch.