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Infusion Pumps

🏥 Medical Devices 4,262 recalls

Potential for spinning versions of male luers to exhibit leaks due to a molding defect. Fluid leakage may potentially cause delay of infusion, contamination of the fluid path, exposure to hazardous medications, blood loss, exposure to patient blood, or fluid path air-in-line.

Aug 31, 2020 Infusion Pumps Nationwide View Details →

Due to footswitch not meeting required specification for protection from ingress of solids or liquids. If spilling of liquids near or on the footswitch, it may fail in the 'on' position and allow the laser to continue to lase.

Oct 16, 2020 Infusion Pumps View Details →

Roche confirmed customer complaints of low quality (QC) recovery and invalid calibrations for the Tina-quant C-Reactive Protein Gen. 3 on the cobas c701 and 702 modules. A discoloration (yellow color) was observed and is the result of cross contamination between the R1 and R3 reagents.

Nov 6, 2020 Infusion Pumps Nationwide View Details →

Due to the incorrect DC/DC converter being assembled onto the communication board. As a result the effectiveness of the communication board cannot be guaranteed in that the safety function of the board would be insufficient resulting in an increased leakage of current and potentially cause electrical shocks to the user.

Aug 6, 2020 Infusion Pumps Nationwide View Details →

Missing solder battery connection, which could interrupt power of insulin pump.

Apr 30, 2020 Infusion Pumps Nationwide View Details →