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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: RANIR LLC KROGER MNTB ORB FL SO 2PK; TOOTHBRUSH, MANUAL

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RANIR LLC KROGER MNTB ORB FL SO 2PK; TOOTHBRUSH, MANUAL Back to Search Results
Model Number MNTB ORB FL SO 2PK
Device Problem Device Dislodged or Dislocated (2923)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 10/14/2019
Event Type  malfunction  
Event Description
Consumer stated bristles fall out of toothbrush during use.No contact information provided to retrieve the product.
 
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Brand Name
KROGER MNTB ORB FL SO 2PK
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
6166988880
MDR Report Key9495454
MDR Text Key178750612
Report Number1825660-2019-00673
Device Sequence Number1
Product Code EFW
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation Other
Type of Report Initial
Report Date 12/19/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/19/2019
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberMNTB ORB FL SO 2PK
Was Device Available for Evaluation? No
Distributor Facility Aware Date11/22/2019
Date Manufacturer Received11/22/2019
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
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