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

MAUDE Adverse Event Report: JOHNSON & JOHNSON CONSUMER INC. LISTERINE ULTRACLEAN MINT FLOSS; FLOSS, DENTAL

  • 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
 

JOHNSON & JOHNSON CONSUMER INC. LISTERINE ULTRACLEAN MINT FLOSS; FLOSS, DENTAL Back to Search Results
Model Number 12547440133
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available (4581)
Event Type  Injury  
Manufacturer Narrative
Device was used for treatment, not diagnosis.Age, weight and ethnicity were not provided for reporting.The lot number was not provided for reporting.Upc = (b)(4), expiration date= na, lot number = ni, udi - (b)(4).Device is not expected to be returned for manufacturer review/investigation.Device evaluation/investigation could not be completed; no conclusion could be drawn as product was not returned to manufacturer.Device history records review could not be completed without the lot number.(b)(4).Consumer reported he bought 12 packs of listerine ultraclean mint floss.He used the floss for 8 months and there are two packs left.As the consumer didn¿t specify if the past used 10 packs of the floss are the same lot as the 2 packs left (lot 11220d captured in medwatch 8041101-2021-00002, lot 12620d captured in medwatch 8041101-2021-00001 and unknown lot, quantity 10 captured in medwatch 8041101-2021-00003 to document the past use.8041101-2021-00001- lot number 12620d, 8041101-2021-00002- lot number 11220d, 8041101-2021-00003 -lot number unknown.If information is obtained that was not available for the initial medwatch, an additional follow-up medwatch will be filed as appropriate.
 
Event Description
Consumer reported an event with listerine ultraclean mint floss 30yd usa.Consumer stated that the floss is plastic.It¿s not like string and has delayed elasticity to it.Consumer reported, damage tooth decay and cavities forming in between the teeth after eight months of using the product.Consumer visited health care professional (hcp) and hcp recommended to have two fillings performed.For further treatment, hcp recommended to switch back to yarn/string type floss.Consumer reported he bought 12 packs of listerine ultraclean mint floss.He used the floss for 8 months and there are two packs left.As the consumer didn¿t specify if the past used 10 packs of the floss are the same lot as the 2 packs left (lot 11220d captured in medwatch (b)(4), lot 12620d captured in medwatch 8041101-2021-00001 and unknown lot, quantity 10 captured in medwatch 8041101-2021-00003 to document the past use.8041101-2021-00001- lot number 12620d, 8041101-2021-00002- lot number 11220d, 8041101-2021-00003 -lot number unknown.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
LISTERINE ULTRACLEAN MINT FLOSS
Type of Device
FLOSS, DENTAL
Manufacturer (Section D)
JOHNSON & JOHNSON CONSUMER INC.
199 grandview road
skillman NJ 08558 9418
Manufacturer (Section G)
JOHNSON & JOHNSON CONSUMER PRODUCTS DR PARQUE INDU
carretera sánchez km. 18.5
haina 91000
DR   91000
Manufacturer Contact
laurie rauco
199 grandview rd
skillman, NJ 08558-9418
2152734905
MDR Report Key11122839
MDR Text Key231959443
Report Number8041101-2021-00003
Device Sequence Number1
Product Code JES
UDI-Device Identifier012547440133
UDI-Public(01)012547440133(10)NI
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 Other
Type of Report Initial
Report Date 12/10/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Model Number12547440133
Was Device Available for Evaluation? No
Event Location Other
Initial Date Manufacturer Received 12/10/2020
Initial Date FDA Received01/06/2021
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
-
-