smiths medical medex CBSS 5 ml, dreifach proximaler Entnahmeport 60 cm, Model number DPSHC0082
Smiths Medical ASD
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
🏥 Medical Devices • 15,809 recalls
Smiths Medical ASD
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Smiths Medical ASD
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Under certain conditions, there is a risk for a false negative result.
Red Medical Supplies
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
Red Medical Supplies
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
Red Medical Supplies
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination. On August 18, 2021,FDA published a Letter to Health Care Providers to further address this issue: https://www.fda.gov/medical-devices/letters-health-care-providers/stop-using-all-eco-med-ultrasound-gels-and-lotions-due-risk-bacterial-contamination-letter-health.
Ultrasound gels and lotions manufactured by Eco-Med Pharmaceutical, Inc. may contain bacterial contamination.
Philips North America
Customers were not notified of previous recalls associated with various defibrillator models.
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Inpeco S.A.
The Firmware (FW) of the Automation System Interface Module to ADVIA Centaur XP/XPT may lead to an incorrect association of test results to sample ID. Improper management of the sample may bring an incorrect patient result.
Beckman Coulter
Missing splash guard which may expose users to hazardous materials. .
Smiths Medical ASD
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Smiths Medical ASD
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Smiths Medical ASD
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Philips North America
Customers were not notified of previous recalls associated with various defibrillator models.
Reported pressure shifts and incorrect pressure readings in LogiCal Closed Blood Sampling System sets.
Bio-Rad Laboratories
A new lot of ANA screen control and any subsequent control lots are incompatible with older lot numbers of ANA calibrators and ANA reagent packs.
Philips North America
Customers were not notified of previous recalls associated with various defibrillator models.
Labeling does not include guidance for proper water-quality maintenance and device inspection for heater cooler devices.