Excessive pressure exerted on the uterine tip when attached to the Arch may, under certain circumstances, cause the internal steel rod of the tip to protrude through the cleaning hole on the shaft of the handle
Surgical Instruments
🏥 Medical Devices • 7,015 recalls
Medtronic is recalling certain Vertex Max Drill Tubes which are used with the StealthStation System due to a defect related to the internal threading for component set up.
Excessive pressure exerted on the uterine tip when attached to the Arch may, under certain circumstances, cause the internal steel rod of the tip to protrude through the cleaning hole on the shaft of the handle
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
Multiple complaints have reported the hex tip of the torque wrench fracturing during final tightening.
SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with Thrombin have an issue within the packing process where a cut could potentially breach the double Tyvek pouch of the packaging.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
SURGIFLO Hemostatic Matrix Kit & SURGIFLO Hemostatic Matrix Kit with Thrombin have an issue within the packing process where a cut could potentially breach the double Tyvek pouch of the packaging.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
Multiple complaints have reported the hex tip of the torque wrench fracturing during final tightening.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.
The product may mislabel patient information on culture specimen bottles due to a software miscommunication.