MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-29 for CAVITRON 300 SERIES ULTRASONIC SCALING SYSTEM UNIT G310 G310SCLR manufactured by Dentsply Llc.
[181482632]
There has been a previous report received where lack of water flow has caused an overheating insert. Since an overheating insert could necessitate medical/surgical intervention to preclude permanent damage to a body structure or permanent impairment of a body function, this malfunction would be likely to cause/contribute to a serious injury should it recur. As such, this event meets the criteria for reportability per 21 cfr part 803.
Patient Sequence No: 1, Text Type: N, H10
[181482633]
Based on the repair notes while using a g310, the water hose was kinked causing low/no water flow causing the sterimate and insert to heat up; no injury resulted.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2424472-2020-00009 |
MDR Report Key | 9772459 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-02-29 |
Date of Report | 2020-02-28 |
Date Mfgr Received | 2020-01-29 |
Date Added to Maude | 2020-02-29 |
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 | DENTIST |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. KARL NITTINGER |
Manufacturer Street | 221 W. PHILADELPHIA ST. SUITE 60W |
Manufacturer City | YORK, PA |
Manufacturer Country | US |
Manufacturer Phone | 8494229 |
Manufacturer G1 | DENTSPLY LLC |
Manufacturer Street | 1301 SMILE WAY |
Manufacturer City | YORK, PA |
Manufacturer Country | US |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CAVITRON 300 SERIES ULTRASONIC SCALING SYSTEM UNIT |
Generic Name | SCALER, ULTRASONIC |
Product Code | ELC |
Date Received | 2020-02-29 |
Returned To Mfg | 2020-01-20 |
Model Number | G310 |
Catalog Number | G310SCLR |
Lot Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DENTSPLY LLC |
Manufacturer Address | 1301 SMILE WAY YORK, PA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-29 |