Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 721–740 of 1,000 recalls
Hitachi Healthcare Americas Corporation
There was no label on the pad packaging or notification in the user manual that the table pads contained dry natural rubber which is required by the Code of Federal Regulations section 21CFR801.437.
Corin Ltd
The packaging system on the devices have potential physical and water damage resulting in damage to the devices, loss of sterility, or contamination of the devices.