MAUDE Adverse Event Report: RANIR LLC EQUATE BR HDS EF II VIP 3PK; TOOTHBRUSH, POWERED

Model Number	BR HDS EF II VIP 3PK
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	06/16/2020
Type of Reportable Event	Malfunction
Event or Problem Description
Consumer stated the bristles on his eq tbp esyflx rf 3ct were falling off/out of 2 of the heads in the pack of 3."i have used the product before with no problems.I bought it about two months ago.Used it until recently.Individual strands of the brush would come loose in my mouth as i was brushing.".

• Brand Name: EQUATE BR HDS EF II VIP 3PK
• Common Device Name: TOOTHBRUSH, POWERED
• Manufacturer (Section D): RANIR LLC; 4701 east paris ave. se; grand rapids MI 49512 5353
• MDR Report Key: 10260374
• Report Number: 1825660-2020-00783
• Device Sequence Number: 596922
• Product Code: JEQ
• UDI-Device Identifier: 00681131129053
• UDI-Public: 681131129053
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: consumer
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 07/10/2020

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
• Operator of Device: Lay User/Patient
• Device Model Number: BR HDS EF II VIP 3PK
• Was Device Available for Evaluation?: No
• Distributor Facility Aware Date: 06/29/2020
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 06/29/2020
• Initial Report FDA Received Date: 07/10/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1