Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 861–880 of 1,000 recalls
Lymol Medical Corporation
Reprocessing instructions were revised November 15, 2020, to reflect new processes and equipment used at consignee user facilities. New instructions were not sent to all consignees of the devices at the time of the revision.
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.