Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) - Product Usage: intended to be used for the controlled administration of fluids.
Baxter Healthcare
There is a potential software error during programming.
🏥 Medical Devices • 4,262 recalls
Baxter Healthcare
There is a potential software error during programming.
Baxter Healthcare
There is a potential software error during programming.
Boston Scientific
Complaint trend regarding needle shaft gas leaks.
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.
Baxter Healthcare
There is a potential software error during programming.
GA HEALTH COMPANY LIMITED
Suction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
GA HEALTH COMPANY LIMITED
Suction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure
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.
Roche Diagnostics Operations
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.
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.
Detachment of the Male AIV Adaptor from the Y-Connector.
During internal testing, it was found that upon a device reset, the Generator exhibits the incorrect Model Number when interrogated.
Randox Laboratories
Failing to meet the linearity performance claims quoted on the kit inserts-The linearity is reduced by approximately -30% for Serum/ Plasma and -50% for Urine
Becton, Dickinson and Company, BD Biosciences
Recent product complaints showing an unexpected cell population exhibiting dim CD3 expression that may result in inaccurate results gating.
Mani, Inc. - Kiyohara Facility
Dimensions of the Luer connector parts out of specification, may cause leakage of fluid and unintended disconnection during use
Randox Laboratories
Failing to meet the linearity performance claims quoted on the kit inserts-The linearity is reduced by approximately -30% for Serum/ Plasma and -50% for Urine
Missing solder battery connection, which could interrupt power of insulin pump.
Missing solder battery connection, which could interrupt power of insulin pump.
Due to a change in handle material and process, probe handle may crack.
Treatment beam information disappears on Treatment Console screen while beam delivery continues potential for harm to a patient could occur