MAUDE Adverse Event Report: C.R. BARD, INC. (COVINGTON) -1018233 PROMAX¿ SERIES BARD® C-MAX¿ CUTTING LOOP; C-MAX CUTTING LOOP

Model Number 355321

Device Problem Break (1069)

Patient Problems No Consequences Or Impact To Patient (2199); No Known Impact Or Consequence To Patient (2692)

Event Type  malfunction  

Manufacturer Narrative

The investigation is still in progress.Once the investigation is complete a supplemental report will be filed.The device was not returned.

Event Description

It was reported that the c-max cutting loop broke during use.There was no patient injury reported.Per follow up with the complainant by email, on (b)(6) 2018, the cutting loop broke while inside of the patient but remained intact when removed.

Manufacturer Narrative

The device was not returned for evaluation.The device history record was reviewed and found nothing that could have caused or contributed to the reported event.The instructions for use were found adequate and state the following: ¿precautions: 1.All medical staff should carefully review product labeling and instruction sheets before using the bard® c-max¿ cutting loop device.Inappropriate use of the instrument could adversely affect the procedure or cause injury to the patient.2.Refer to the applicable operating and maintenance manuals for the resectoscope and electrosurgical generator being used.3.The bard® c-max¿ cutting loop device should be used only by a physician who is familiar with the use of electrosurgical instruments, devices and power generators.Consult the medical literature regarding techniques, typical power settings, complications, and hazards prior to any endoscopic procedure.4.During application of electrical energy, movement of the tip is required to achieve the desired tissue effect.5.The time and energy required for treating specific tissue may differ when using the bard® c-max¿ cutting loop device compared to other electrosurgical devices.6.The monopolar electrosurgical generator should be set to the cut or pure cut mode for maximum tissue removal effect.Do not use the blend mode and be cautious of arcing on high coagulation power settings.7.Starting at power settings consistent with standard resectoscope cutting loop procedures, gradually increase power until the desired tissue effect is achieved.If there is little or no tissue effect, check the generator, power and grounding cables and the electrodes.Various electrosurgical generators have different power delivery capabilities.Depending on the impedance in the monopolar circuit, the power delivered may be lower than the power setting indicates (see owner/operator manual for the generator being used).8.Constant irrigation is required throughout the procedure, and the distal tip of the device should be submerged and kept in view at all times.Use sterile non-conductive irrigation solution only.9.Immediately discontinue use if breaks or fractures appear in the bard® c-max¿ cutting loop device.Breaks or fractures may allow undirected emission of electrical energy, rendering the device useless and potentially causing harm to surrounding tissues.10.Do not bend or manipulate the device.11.Care should be taken to avoid severe impacts, side stresses or bends at sharp angles.12.When endoscopic devices are used together, ensure that any isolation or ground is not violated.Indications for use: the bard® c-max¿ cutting loop device is indicated for resection of soft tissue including procedures for the treatment of benign prostatic hypertrophy (bph).It is intended for use with compatible resectoscopes.Device description: the bard® c-max¿ cutting loop device is a monopolar electrode designed to deliver radio frequency energy that is supplied by an electrosurgical generator cleared for medical use.Information for use caution, consult accompanying documents.Directions for use: 1.Remove the bard® c-max¿ cutting loop device from the package and examine it for damage.Do not use if there are visible signs of damage or insulation is not intact.2.Assemble the working element and resectoscope according to the instructions provided by the resectoscope manufacturer.3.Insert the bard® c-max¿ cutting loop device into the working channel of the resectoscope per instructions indicated in the resectoscope operating manual.4.Ensure that the electrode is securely placed and locked into position by pulling carefully on the electrode stabilizer sleeve (if appropriate).5.Attach resectoscope to the electrosurgical generator according to manufacturer's recommendations.6.Insert the combined assembly into the resectoscope sheath and position at the point where initial application of electrical energy will be delivered.7.Unless recommended by other sources, the electrosurgical generator should be set on the pure cut setting at power levels consistent with standard resectoscope cutting loop procedures".

Event Description

It was reported that the c-max cutting loop broke during use.There was no patient injury reported.Per follow up with the complainant by email, on (b)(6) 2018, the cutting loop broke while inside of the patient but remained intact when removed.

• Brand Name: PROMAX¿ SERIES BARD® C-MAX¿ CUTTING LOOP
• Type of Device: C-MAX CUTTING LOOP
• Manufacturer (Section D): C.R. BARD, INC. (COVINGTON) -1018233; 8195 industrial blvd; covington GA 30014
• MDR Report Key: 8120784
• MDR Text Key: 129038148
• Report Number: 1018233-2018-05767
• Device Sequence Number: 1
• Product Code: FAS
• UDI-Device Identifier: 00801741018596
• UDI-Public: (01)00801741018596
• Combination Product (y/n): N
• PMA/PMN Number: EXEMPT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: other,user facility
• Type of Report: Initial,Followup
• Report Date: 02/08/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/30/2018
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 03/08/2021
• Device Model Number: 355321
• Device Catalogue Number: 355321
• Device Lot Number: NGAS1748
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 01/21/2019
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1