MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign report with the FDA on 2019-12-31 for PHILIPS SONICARE HX8240 HX8211/02 manufactured by Philips Oral Healthcare, Llc.
[173965373]
Outcomes to adverse event: the consumer reported that the front of a molar broke off. Report source: complaint received from the (b)(6).
Patient Sequence No: 1, Text Type: N, H10
[173965474]
A consumer alleged that the airfloss caused the front of a molar to break off during use.
Patient Sequence No: 1, Text Type: D, B5
[189091691]
Correction of the product model number; revised lot # from not applicable (na) to no information (ni). Analysis results: the root cause of the customer's complaint could not be determined as the device operates within specification.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3026630-2019-00083 |
MDR Report Key | 9537065 |
Report Source | CONSUMER,FOREIGN |
Date Received | 2019-12-31 |
Date of Event | 2019-12-05 |
Date Facility Aware | 2019-12-05 |
Date Mfgr Received | 2020-03-04 |
Device Manufacturer Date | 2019-06-06 |
Date Added to Maude | 2019-12-31 |
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. CHIEU YEUNG |
Manufacturer Street | 22100 BOTHELL EVERETT HIGHWAY |
Manufacturer City | BOTHELL WA 98021 |
Manufacturer Country | US |
Manufacturer Postal | 98021 |
Manufacturer Phone | 4254877000 |
Manufacturer G1 | PHILIPS ORAL HEALTHCARE, LLC |
Manufacturer Street | 22100 BOTHELL EVERETT HIGHWAY |
Manufacturer City | BOTHELL WA 98021 |
Manufacturer Country | US |
Manufacturer Postal Code | 98021 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PHILIPS SONICARE |
Generic Name | AIRFLOSS |
Product Code | EFS |
Date Received | 2019-12-31 |
Returned To Mfg | 2020-01-13 |
Model Number | HX8240 |
Catalog Number | HX8211/02 |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS ORAL HEALTHCARE, LLC |
Manufacturer Address | 22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 98021 US 98021 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-12-31 |