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Surgical Instruments

🏥 Medical Devices 7,015 recalls

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

Oct 31, 2012 Surgical Instruments Nationwide View Details →

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.

Nov 13, 2012 Surgical Instruments Nationwide View Details →

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

Oct 31, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

Multiple complaints have reported the hex tip of the torque wrench fracturing during final tightening.

Aug 9, 2012 Surgical Instruments Nationwide View Details →

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.

Aug 21, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

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.

Aug 21, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

Multiple complaints have reported the hex tip of the torque wrench fracturing during final tightening.

Aug 9, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →

The product may mislabel patient information on culture specimen bottles due to a software miscommunication.

Oct 16, 2012 Surgical Instruments Nationwide View Details →