PHILIPS SONICARE HX8240 HX8211/02

MAUDE Adverse Event Report

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.

Event Text Entries

[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


MAUDE Entry Details

Report Number3026630-2019-00083
MDR Report Key9537065
Report SourceCONSUMER,FOREIGN
Date Received2019-12-31
Date of Event2019-12-05
Date Facility Aware2019-12-05
Date Mfgr Received2020-03-04
Device Manufacturer Date2019-06-06
Date Added to Maude2019-12-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. CHIEU YEUNG
Manufacturer Street22100 BOTHELL EVERETT HIGHWAY
Manufacturer CityBOTHELL WA 98021
Manufacturer CountryUS
Manufacturer Postal98021
Manufacturer Phone4254877000
Manufacturer G1PHILIPS ORAL HEALTHCARE, LLC
Manufacturer Street22100 BOTHELL EVERETT HIGHWAY
Manufacturer CityBOTHELL WA 98021
Manufacturer CountryUS
Manufacturer Postal Code98021
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePHILIPS SONICARE
Generic NameAIRFLOSS
Product CodeEFS
Date Received2019-12-31
Returned To Mfg2020-01-13
Model NumberHX8240
Catalog NumberHX8211/02
OperatorLAY USER/PATIENT
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS ORAL HEALTHCARE, LLC
Manufacturer Address22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 98021 US 98021


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-12-31

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