MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2016-08-02 for BUSH URETERAL ILLUMINATING CATHETER SET 084120 manufactured by Cook Inc.
[50920161]
(b)(4). The event is currently under investigation.
Patient Sequence No: 1, Text Type: N, H10
[50920162]
During a laparoscopic colectomy with cystoscopic stent placement procedure, the device started to melt where the stent attaches to the black casing that connects to the light source. This was not noticed until the procedure had been completed. A section of the device did not remain inside the patient's body. According to the initial reporter, the patient did not require any additional procedures nor experience any adverse effects due to this occurrence.
Patient Sequence No: 1, Text Type: D, B5
[65820995]
Investigation - evaluation a review of the complaint history, device history record, instructions for use (ifu), manufacturing instructions, specifications, quality control and visual inspection of the returned device was conducted during the investigation. The device is shipped with an instruction for use (ifu) that describes the intended use, specific items are addressed such as: this catheter will not transmit thermal energy along its light fibers to patient tissue. Any excessive thermal damage from the light source will manifest at the catheter/light plug junction, and will not be transmitted along the catheter length. Start illumination with the light source at the lowest setting, as many light sources product thermal energy at varying temperatures. This will limit the possibility of thermal damage at the catheter/light plug junction. It is inadvisable to use any light source at its highest setting, unless the light source`s actual thermal energy output is unknown. The visual inspection of the returned device reported: the clear illumination section of the device was not returned. There appears to be a region approximately 2mm in total length, where the outer sheathing is melted. Adjacent to the melting there is some shiny unidentified material that appear to have run down the exterior of the device when liquid. The plug on the device was noted as being secure. There is a knick in the exterior sheathing 15cm from the spring. The complaint device was returned therefore, an investigation evaluation was performed. There is no evidence to suggest the product was not made to specifications. It should be noted there were no other reported complaints for this lot number. Based on the information provided, and the results of our investigation, it was hypothesized that the device had experienced melting due to excessive thermal energy as noted in the ifu. We will continue to monitor for similar complaints. Per the quality engineering risk assessment no further action is required.
Patient Sequence No: 1, Text Type: N, H10
[65820996]
During a laparoscopic colectomy with cystoscopic stent placement procedure, the device started to melt where the stent attaches to the black casing that connects to the light source. This was not noticed until the procedure had been completed. A section of the device did not remain inside the patient? S body. According to the initial reporter, the patient did not require any additional procedures nor experience any adverse effects due to this occurrence.
Patient Sequence No: 1, Text Type: D, B5
[70785014]
(b)(4). Investigation - evaluation a review of the complaint history, device history record, instructions for use (ifu), manufacturing instructions, specifications, quality control and visual inspection of the returned device was conducted during the investigation. The device is shipped with an instruction for use (ifu) that describes the intended use, specific items are addressed such as: this catheter will not transmit thermal energy along its light fibers to patient tissue. Any excessive thermal damage from the light source will manifest at the catheter/light plug junction, and will not be transmitted along the catheter length. Start illumination with the light source at the lowest setting, as many light sources produce thermal energy at varying temperatures. This will limit the possibility of thermal damage at the catheter/light plug junction. It is inadvisable to use any light source at its highest setting, unless the light source`s actual thermal energy output is unknown. The visual inspection of the returned device reported: the clear illumination section of the device was not returned. There appears to be a region approximately 2mm in total length, where the outer sheathing is melted. Adjacent to the melting there is some shiny unidentified material that appear to have run down the exterior of the device when liquid. The plug on the device was noted as being secure. There is a knick in the exterior sheathing 15cm from the spring. A document based investigation evaluation was also performed. There is no evidence to suggest the product was not made to specifications. Review of device history record shows no nonconforming events which could contribute to this failure mode. It should be noted there were no other reported complaints for this lot number. Based on the information provided, examination of the returned device and the results of our investigation, it was hypothesized that the device experienced melting due to excessive thermal energy as noted in the ifu. We will continue to monitor for similar complaints. Per the quality engineering risk assessment no further action is required.
Patient Sequence No: 1, Text Type: N, H10
[70785015]
During a laparoscopic colectomy with cystoscopic stent placement procedure, the device started to melt where the stent attaches to the black casing that connects to the light source. This was not noticed until the procedure had been completed. Additional information was requested. The customer advised that there are no records of harm to the staff or patient. Details of the device use, light source type and settings are not available. The catheters were removed by hand at the end of the procedure. A section of the device did not remain inside the patient? S body. According to the initial reporter, the patient did not require any additional procedures nor experience any adverse effects due to this occurrence. No further information will be provided by the customer as when the customer was called back she stated, " she had no recollection of the event and stated she would not have any records of it. " the instructions for use that accompany each device states under the precautions section that " the anodized aluminum plug conducts heat. Allow the plug to cool down prior to attempting to unplug. " the instructions for use also state under the instructions for use section that: " note: this catheter will not transmit thermal energy along its light fibers to patient tissue. Any excessive thermal damage from the light source will manifest at the catheter/light plug junction and will not be transmitted along the catheter length. " "note: high-energy light sources such as xenon may cause overheating of the anodized aluminum plug. An adapter (available from most light source manufacturers) will ensure product safety and functionality. " "note: start illumination with the light source at the lowest setting, as many light sources produce thermal energy at varying temperatures. This will limit the possibility of thermal damage at the catheter/light plug junction. "
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1820334-2016-00704 |
| MDR Report Key | 5839561 |
| Report Source | COMPANY REPRESENTATIVE |
| Date Received | 2016-08-02 |
| Date of Report | 2017-07-18 |
| Date of Event | 2016-07-01 |
| Date Mfgr Received | 2017-06-30 |
| Device Manufacturer Date | 2015-08-24 |
| Date Added to Maude | 2016-08-02 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. LARRY POOL |
| Manufacturer Street | 750 DANIELS WAY |
| Manufacturer City | BLOOMINGTON IN 47404 |
| Manufacturer Country | US |
| Manufacturer Postal | 47404 |
| Manufacturer Phone | 8123392235 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | Z-1870-2017 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BUSH URETERAL ILLUMINATING CATHETER SET |
| Generic Name | FCS CATHETER, LIGHT, FIBEROPTIC, GLASS, URETERAL |
| Product Code | FCS |
| Date Received | 2016-08-02 |
| Model Number | NA |
| Catalog Number | 084120 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COOK INC |
| Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2016-08-02 |