• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: RANIR LLC CAREONE; TOOTHBRUSH, MANUAL

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

RANIR LLC CAREONE; TOOTHBRUSH, MANUAL Back to Search Results
Model Number MNTB MLTFT PL SO 4PK
Device Problem Component Falling (1105)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 09/19/2017
Event Type  malfunction  
Event Description
Consumer stated the bristles just fall out of the toothbrushes as they are using them.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
CAREONE
Type of Device
TOOTHBRUSH, MANUAL
Manufacturer (Section D)
RANIR LLC
4701 east paris ave. se
grand rapids MI 49512 5353
Manufacturer (Section G)
RANIR LLC
4701 east paris ave. se
grand rapids MI 49512 5353
Manufacturer Contact
rebekah stenske
4701 east paris ave. se
grand rapids, MI 49512-5353
6166988880
MDR Report Key6948864
MDR Text Key90470968
Report Number1825660-2017-00179
Device Sequence Number1
Product Code EFW
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation Patient
Type of Report Initial
Report Date 10/13/2017
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberMNTB MLTFT PL SO 4PK
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Distributor Facility Aware Date09/19/2017
Initial Date Manufacturer Received 09/19/2017
Initial Date FDA Received10/13/2017
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
-
-