Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 861–880 of 1,000 recalls
Philips North America LLC
Infant/Child defibrillator pads contain incorrect labeling. This could lead to a delay in therapy, or delivery of lower energy than indicated for an adult patient
Beckman Coulter Inc.
There is a potential that the data management system may add additional cells to the patient request which could lead to erroneous patient result.