All Recalls

95,114 total recalls in our database

The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the device has been associated with breakage of the insertion section and protrusion of metal parts, as well as breakage and displacement of the rubber on the bending section during surgical procedures.

Aug 31, 2020 Diagnostic Equipment Nationwide View Details →

Plastic socket of the IEC 60320-1 socket pulled out of the metal cage and electronic parts exposed; where the socket was pulled out and main cable is still connected to the main socket (power source), there is a risk that a user or third person may suffer an electric shock when coming in contact with the exposed electronic components

Sep 24, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →

The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

Sep 11, 2020 Surgical Instruments Nationwide View Details →

Subsequent failure of catheters in the field and failed quality testing

Aug 25, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →

Identification of a potential manufacturing defect on the internal surface of the NanoClave within specific lots of NanoClave sets, which may inhibit a proper seal with the NanoClave spike.

Jul 6, 2020 Surgical Instruments Nationwide View Details →