Loading...
Loading...
All product recalls associated with Philips Medical Systems.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
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.
Instructions For Use include addtional information on configuration for selecting Power on Lead
Software errors cause the unit to not deliver the prescribed therapy and do not allow the patient records to be saved.
The firm's DP8200 Microflow Needle Packs were labeled with the firm's DP8115 Phaco Needle Packs and visa versa.