MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-02-08 for LUXSTAR STANDARD POST-MOUNT LIGHT UL1000 manufactured by Marus.
[67243485]
The lens heat shield/holder from the dental light has a three prong locking mechanism which locks the lens heat shield/cover into place. The lens heat shield/cover has to be removed by the end user when cleaning the lens or replacing the halogen bulb during routine operator maintenance. The installation instructions, use and care instructions, and labeling clearly state to ensure the lens heat shield/holder is properly secure by snapping the part back into place. Marus initiated a recall on june 10, 2011 to add a tether to the lens heat shield/cover to keep it from falling off the dental light if it is not re-installed properly. The fda closed this recall on 10/26/2012 (please reference fda recall z-2834-2011). Marus notified all distributors of the recall while the recall was open. The doctor and his current service provider could not locate the serial number on this particular light. They both informed marus the light was very old and the serial number tag must have somehow been removed. After following back up with the dentist on 2/8/2017, the dental office informed marus the tether was installed on the dental light and it is working properly.
Patient Sequence No: 1, Text Type: N, H10
[67243486]
A dental professional was treating a patient when the lens heat shield cover fell off a marus dental light hitting the patient on the neck causing a small burn. There were no serious injuries reported. No medical attention was required.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1017522-2017-00005 |
| MDR Report Key | 6312880 |
| Date Received | 2017-02-08 |
| Date of Report | 2017-01-13 |
| Date of Event | 2017-01-13 |
| Date Mfgr Received | 2017-01-13 |
| Date Added to Maude | 2017-02-08 |
| 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 |
| Reporter Occupation | MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MR. FRANK RAY |
| Manufacturer Street | 11727 FRUEHAUF DRIVE |
| Manufacturer City | CHARLOTTE NC 28273 |
| Manufacturer Country | US |
| Manufacturer Postal | 28273 |
| Manufacturer Phone | 7045877227 |
| Manufacturer G1 | MARUS |
| Manufacturer Street | 11727 FRUEHAUF DRIVE |
| Manufacturer City | CHARLOTTE NC 28273 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 28273 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | LUXSTAR STANDARD POST-MOUNT LIGHT |
| Generic Name | DENTAL LIGHT |
| Product Code | EAZ |
| Date Received | 2017-02-08 |
| Model Number | UL1000 |
| Catalog Number | UL1000 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MARUS |
| Manufacturer Address | 11727 FRUEHAUF DRIVE CHARLOTTE NC 28273 US 28273 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-02-08 |