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

MAUDE Adverse Event Report: WATER PIK INC. WATER PIK POWERPULSE HEIGHT SELECT MAGNETIC SLIDE STRIP SHOWER SYSTEM; SHOWER HEAD

  • 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
 

WATER PIK INC. WATER PIK POWERPULSE HEIGHT SELECT MAGNETIC SLIDE STRIP SHOWER SYSTEM; SHOWER HEAD Back to Search Results
Model Number XHS-763MVB
Device Problem Device Fell (4014)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 08/28/2023
Event Type  malfunction  
Event Description
Magnetic sh installed a month ago & fell off wall.No medical attention was sought and no injury occurred.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
WATER PIK POWERPULSE HEIGHT SELECT MAGNETIC SLIDE STRIP SHOWER SYSTEM
Type of Device
SHOWER HEAD
Manufacturer (Section D)
WATER PIK INC.
1730 e prospect rd
fort collins CO
Manufacturer Contact
jeffrey dornoff
1730 e prospect rd
fort collins, CO 80553-0001
9702217062
MDR Report Key17814331
MDR Text Key324369287
Report Number0001712259-2023-00018
Device Sequence Number1
Product Code LYG
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
EXEMPT
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Administrator/Supervisor
Remedial Action Replace
Type of Report Initial
Report Date 09/25/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/25/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberXHS-763MVB
Device Lot NumberUNKNOWN
Was Device Available for Evaluation? No
Date Manufacturer Received08/28/2023
Was Device Evaluated by Manufacturer? No
Date Device Manufactured11/09/2022
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
Patient Outcome(s) Other;
Patient SexMale
Patient EthnicityNon Hispanic
Patient RaceWhite
-
-