All Recalls

95,025 total recalls in our database

The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the the correct part number 1747065, NVM5 Harness, Gen 3.5 EM. This issue can result in delay in therapy or lack of EMG neuromonitoring during surgery if the surgeon elects to proceed without the NVM5.

Jun 10, 2020 Diagnostic Equipment Nationwide View Details →

Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.

Jun 8, 2020 Infusion Pumps Nationwide View Details →

Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.

Jun 8, 2020 Infusion Pumps Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

The Universal Drainage Set (UDS) may contain valves that leak internally which may result in the introduction of up to 30cc of air into the patient.

May 28, 2020 Surgical Instruments Nationwide View Details →
🏥 Medical Devices Class I - Dangerous

Some Intellivue MX700/MX800 Patient Monitors were delivered with defective power supplies. The defective power supplies might energize the metal parts of monitor if the grounding instructions were not followed, and may also cause the monitor to stop operating or prevent it from being switched on.

Jun 30, 2020 Diagnostic Equipment View Details →

Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.

Jun 8, 2020 Infusion Pumps Nationwide View Details →

Insertion difficulty of the probes. The probe was catching on a lip inside the hub of the cannula.

Jun 8, 2020 Infusion Pumps Nationwide View Details →

Potential development of cracks or breaks in the tubing near the Luer or Y site of the device. Devices that have developed breaks or cracks can cause leakage resulting in exposure to chemicals such a chemotherapeutics or biohazard material (e.g., blood). A crack or break could result in potential blood loss, catheter occlusion, air embolism, under or interrupted infusion, or site contamination which could lead to infection.

Jun 19, 2020 Surgical Instruments View Details →

Two issues were identified with the computed tomography x-ray system including a service function which may cause false marking of a bad channel resulting in ring artifacts, and potential intermittent scout scanning interruption due to occasional angle signal drift.. If these problems occur, it may be necessary to rescan the patient resulting in an additional dose of radiation and the possible need for additional contrast medium.

May 23, 2020 Other Medical Devices View Details →