• 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 MEIJER MTH GD RST ASRD W/TRAY 2CT; MOUTHGUARD, OVER-THE-COUNTER

  • 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 MEIJER MTH GD RST ASRD W/TRAY 2CT; MOUTHGUARD, OVER-THE-COUNTER Back to Search Results
Model Number MTH GD RST ASRD W/TRAY 2CT CRTN
Device Problems Break (1069); Material Integrity Problem (2978)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 07/21/2020
Event Type  malfunction  
Event Description
Consumer stated after fitting the first guard and using it for about 3 weeks, the guard broke and split into two during use at the middle where it was very thin.Consumer threw away the guard.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
MEIJER MTH GD RST ASRD W/TRAY 2CT
Type of Device
MOUTHGUARD, OVER-THE-COUNTER
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 Key10417982
MDR Text Key204393075
Report Number1825660-2020-00792
Device Sequence Number1
Product Code OBR
UDI-Device Identifier00719283190390
UDI-Public719283190390
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K133423
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation Other
Type of Report Initial
Report Date 08/17/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/17/2020
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberMTH GD RST ASRD W/TRAY 2CT CRTN
Device Lot Number287842
Was Device Available for Evaluation? No
Distributor Facility Aware Date07/21/2020
Date Manufacturer Received07/21/2020
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
-
-