It was reported about a 9 mm flexible drill that, during an unknown procedure, broke while drilling the femoral tunnel.It is unknown if a back-up device was available or if there was a delay in the scheduled surgery.No patient injuries or other complications were reported.All available information has been disclosed.If additional information should become available, a supplemental report will be submitted accordingly.
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H10: h3, h6: one 7209738 flexible 9mm endoscopic cannulated drill used for treatment, was not returned for evaluation.This device was over 5 years old at time of use.It had exceeded its expiration.Due to unavailability, investigation and evaluation were limited.If further information becomes available, the complaint may be revisited.Factors that may affect device performance include: device storage, device ability, surgical ability, procedure location and tissue condition.Influences that could compromise product performance or integrity include: 1.Condition the driver¿s bit or chuck.2.Use of reverse rotation.3.Inadvertent torque, pressure, leverage and bending.4.Getting entangled up with other instruments or devices.5.Debris such as bone chips caught in the bit or chuck.6.Unexpected bone density/condition.Per instructions for use: ¿never use the drill in reverse rotation.Only use the drill in forward rotation.Using the drill in reverse rotation may result in patient injury and/or failure of the instrument.This is a limited reuse device based upon the sharpness of the drill tip.As with any surgical instrument, careful attention must be exercised to ensure that excessive force is not placed on the instrument.Excessive force can result in instrument failure.Do not use these instruments as levers for manipulating hard tissue or bone.Excessive force should not be applied to the instrument when manipulating soft tissue, bone, or hard objects.Misuse of these instruments may result in bent distal tips or jaws; and dull or uneven cutting edges¿.This product is intended to flex but not be bent.Complaint history review indicated no similar allegations for the lot number reported.Batch review did not indicate a condition or product/procedure failure that supported the allegation.Product met specifications upon release to distribution.No additional actions required at this time.
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