Tissu-Trans MEGA 1500, 3-TT-MEGA 1500. Product Usage: Intended for fat transfer and liposuction.
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Medical equipment, implants, and diagnostic devices
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Alcon Research
Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software coding error that results in the lens coefficients for an IOL model being downloaded from the Alcon server in an incorrect order.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Medtronic received reports that the DBS depth stop did not adequately secure to the lead, which can result in DBS lead placement beyond the intended target.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
The firm manufactured and distributed custom surgical kits which contained BD SafetyGlide" 22GA 1Âŋ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection.
Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used with EG-3670URK and EG-3870UTK ultrasound gastroscopes. In the disinfection step, the IFU has a warning indicating the cleaning detergent solution should remain in contact with the all internal channels and external endoscope surfaces. The disinfecting solution, not the cleaning detergent, should be used for this step.
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Alcon Research
Some ORA Carts have the potential to return an incorrect IOL power measurement during cataract surgery. This issue appears to have been caused by a software coding error that results in the lens coefficients for an IOL model being downloaded from the Alcon server in an incorrect order.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Potential inaccurate calibration by service depot repair, which could contribute to patients being burnt by the device. This only impacts units serviced between the dates of 09/08/2016 and 05/23/2017.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Potential inaccurate calibration by service depot repair, which could contribute to patients being burnt by the device. This only impacts units serviced between the dates of 09/08/2016 and 05/23/2017.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.
Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used with EG-3670URK and EG-3870UTK ultrasound gastroscopes. In the disinfection step, the IFU has a warning indicating the cleaning detergent solution should remain in contact with the all internal channels and external endoscope surfaces. The disinfecting solution, not the cleaning detergent, should be used for this step.
Shippert Medical Technologies
Seal integrity of the Tissu-Trans product sterile packages cannot be assured.
Cardinal Health 200
Product 29474 LAVH drape was packaged as 29574 Robotic Drape with Leggings.