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

MAUDE Adverse Event Report: THE HONEY POT COMPANY LLC. THE HONEY POT COMPANY EVERYDAY HERBAL-INFUSED PANTILINERS; PADS, MENSTRUAL, SCENTED-DEODORIZED

  • 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
 

THE HONEY POT COMPANY LLC. THE HONEY POT COMPANY EVERYDAY HERBAL-INFUSED PANTILINERS; PADS, MENSTRUAL, SCENTED-DEODORIZED Back to Search Results
Device Problem Product Quality Problem (1506)
Patient Problems Pain (1994); Burning Sensation (2146)
Event Date 10/11/2021
Event Type  Injury  
Event Description
I bought the honey pot company everyday herbal infused pantiliners (for menstrual periods).I had it on for maybe 2-3 minutes and it burned and stung my private parts.I had to take it off and it continued to burn for another 30 minutes.Apparently it was meant to be "soothing." it is very much not soothing and was very painful.I can't believe this is allowed to be sold.Things are sensitive down there.(fda#(b)(4)).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
THE HONEY POT COMPANY EVERYDAY HERBAL-INFUSED PANTILINERS
Type of Device
PADS, MENSTRUAL, SCENTED-DEODORIZED
Manufacturer (Section D)
THE HONEY POT COMPANY LLC.
490 marietta st. nw
ste 107
atlanta GA 30313
MDR Report Key12638705
MDR Text Key277087172
Report NumberMW5104639
Device Sequence Number1
Product Code HIL
Combination Product (y/n)Y
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 10/12/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received10/14/2021
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator No Information
Was Device Available for Evaluation? Yes
Was Device Evaluated by Manufacturer? No Information
Type of Device Usage N
Patient Sequence Number1
Patient Age46 YR
Patient Weight99
-
-