MEDLINE

Description of Event or Problem

IT WAS REPORTED THAT THE SHOWER CHAIUR LEG, IS THE WRONG LEG, AND DOESN'T FIT UNIT PROPERLY. SHE WAS ABLE TO INSTALL IT, BUT THE HOLES FOR THE LEGEXTENSION ARE DILLED IN THE WRONG SPOT, AND THE LEG IS SHORTER. SHE ADVISED THERE ARE NO LORE HOLES THAT WOULD MAKE IT LEVEL, AND IT IS INSTALLED CORRETLY.

Additional Manufacturer Narrative

IT WAS REPORTED THAT THE SHOWER CHAIUR LEG, IS THE WRONG LEG, AND DOESN'T FIT UNIT PROPERLY. SHE WAS ABLE TO INSTALL IT, BUT THE HOLES FOR THE LEG EXTENSION ARE DILLED IN THE WRONG SPOT, AND THE LEG IS SHORTER. SHE ADVISED THERE ARE NO LORE HOLES THAT WOULD MAKE IT LEVEL, AND IT IS INSTALLED CORRETLY. THERE WERE NO REPORTS OF DEATH, SERIOUS INJURY, MEDICAL INTERVENTION, OR FOLLOW UP CARE. IT HAS BEEN DETERMINED THAT THE REPORTED EVENT COULD CAUSE OR CONTRIBUTE TO SERIOUS INJURY IF IT WERE TO OCCUR AGAIN. IN AN ABUNDANCE OF CAUTION, THIS IS A REPORTABLE EVENT. IF ADDITIONAL INFORMATION BECOMES AVAILABLE THIS REPORT WILL BE REOPENED AND REEVALUATED. THIS MEDICAL DEVICE REPORT (MDR) IS BEING SUBMITTED AS PART OF RETROSPECTIVE REVIEW ACTIVITIES, WHICH INCLUDE REVIEW OF HISTORICAL DATA IN ACCORDANCE WITH REGULATIONS AT 21 CFR PART 803. THE INFORMATION INCLUDED IN THIS MDR REFLECTS THE INFORMATION REASONABLY KNOWN TO THE MANUFACTURER AT THE TIME OF THIS RETROSPECTIVE REVIEW AND SUBMISSION.