MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2018-11-21 for ILLUMINOSS PHOTODYNAMIC BONE STABILIZATION SYSTEM SL-1700260 manufactured by Illuminoss Medical Inc.
[128097814]
The device was not returned to illuminoss for evaluation. The final assessment of how the device was punctured based on the information received, was that it was due to the surgeon attempting to reduce the fracture with a bone span during the filling of the implant. The surgeon's guide for this product cautions the user that damage to the implant may occur if the implant or bone is moved while the implant is in place and inflated. In regards to the light box not being operational, it is specified in the pre-operational set-up section of the surgeons guide to turn on the light box before starting the procedure. This did not happen as the light box was turned on after the second implant was inserted and inflated.
Patient Sequence No: 1, Text Type: N, H10
[128097815]
On (b)(6) 2018, during a repair of a fracture of the humerus, an illuminoss implant was damaged during an attempted reduction of the fracture using a bone span while the balloon was being filled. After it was determined that the implant was damaged, the damaged implant and monomer were removed from the canal. It should be noted that the surgeon's guide states that prior to attempting to move either the implant or bone after the implant is in place and inflated, the user is to deflate the implant or damage to the implant may occur. It was reported that during the filling of this first balloon, and prior to it being damaged, the patient experienced a minor cardiac event. The procedure continued once the patient was stabilized without any further complications. After the first implant and monomer were removed, a second implant was prepared, inserted and filled with monomer. Once the second balloon was filled, the lightbox was turned on. It should be noted that the light box had not been started to this point of the procedure. Upon turning the light box on, the "change bulb" indicator light came on that requires the bulb to be changed before it can be used. It was reported that the user facility did not have a spare bulb. Without an operational light box, the illuminoss system cannot be used. It should be noted that the surgeon's guide instructs the user to turn on the light box prior to the start of the procedure to ensure that it is operational. Once it was determined that the lightbox was not operational, the second implant was removed without incident. Subsequent to the removal of the second implant, the surgeon used a plate and screws to secure the fracture. Once this was completed, the patient began showing signs of difficulty coming out of anesthesia and was not able to be stabilized. They subsequently expired.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3006845464-2018-00005 |
| MDR Report Key | 8095934 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2018-11-21 |
| Date of Report | 2018-11-20 |
| Date of Event | 2018-10-24 |
| Date Mfgr Received | 2018-10-24 |
| Device Manufacturer Date | 2018-04-30 |
| Date Added to Maude | 2018-11-21 |
| 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 ROBERT RABINER |
| Manufacturer Street | 993 WATERMAN AVENUE |
| Manufacturer City | EAST PROVIDENCE RI 02914 |
| Manufacturer Country | US |
| Manufacturer Postal | 02914 |
| Manufacturer Phone | 4017140008 |
| Manufacturer G1 | ILLUMINOSS MEDICAL INC |
| Manufacturer Street | 993 WATERMAN AVENUE |
| Manufacturer City | EAST PROVIDENCE RI 02914 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 02914 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ILLUMINOSS PHOTODYNAMIC BONE STABILIZATION SYSTEM |
| Generic Name | IN-VIVO CURED INTRAMEDULLARY FIXATION ROD |
| Product Code | QAD |
| Date Received | 2018-11-21 |
| Catalog Number | SL-1700260 |
| Lot Number | 380465 |
| Device Expiration Date | 2019-06-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ILLUMINOSS MEDICAL INC |
| Manufacturer Address | 993 WATERMAN AVENUE EAST PROVIDENCE RI 02914 US 02914 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Death | 2018-11-21 |