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All product recalls associated with Philips Medical Systems.
Total Recalls
1000
Past Year
583
Class I (Serious)
91
Most Recent
Dec 2025
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.
Potential for shock treatment to be delayed or prevented due to board contamination that causes intermittent switch operation
Due to a manufacturing error, the proximal end may deform causing the protrusions that engage the associated implant to break off of the instrument during use.
The handpiece package may have an incorrect part number on the inner package. Error could result in over-penetration of the biopsy needle.