Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems castors were replaced with a new castor design because investigation found the old design had the potential for the casters to bind compromising the Rover's ability to roll. This can result in additional strain on the operator, due to multiple exposures resulting in back pain.
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Surgical Instruments
🏥 Medical Devices • 6,839 recalls
Failure of glue joint, allowed a portion of the single use device to shift inside, may separate and fall into the patient
Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems castors were replaced with a new castor design because investigation found the old design had the potential for the casters to bind compromising the Rover's ability to roll. This can result in additional strain on the operator, due to multiple exposures resulting in back pain.
Class I - Dangerous
Product Event Reports revealed a broken reamer experienced intra-operatively. Pre-drilling was not performed prior to reaming.
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
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.