FDA Adverse Event Injury Summary report: N

TEE PEE

MDR report key: 1056183 · Received June 4, 2008

Report

Report Number
MW5007126
Event Type
Injury
Date Received
June 4, 2008
Date of Event
December 14, 2007
Report Date
May 14, 2008
Manufacturer
MEDICAL SPECIALTIES
Product Code
FYH
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
CA
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

TEE PEE THUMB SPLINT WORN THREE DAYS CUT MY WRIST RESULTING IN WRIST PAIN, AS WELL AS THUMB PAIN FOR WHICH SPLINT WAS PRESCRIBED BY DOCTOR. THE PLASTIC "STAY" CUT INTO MY WRIST BELOW, THE THUMB (ON RIGHT HAND) CAUSING PAIN. I STOPPED USE AFTER 3 DAYS, BUT PAIN IN WRIST REMAINS. NOTE: I HAVE SEEN MY DOCTOR THREE TIMES, HAVE SEEN AN ORTHOPEDIC SPECIALIST ONCE, VISITED PHYSIOTHERAPIST FOR ONE MONTH, RECEIVED MASSAGE THERAPY THE PAST FOUR MONTHS. I WEAR THE SPLINT 70%-90% OF EACH DAY (TAKEN OFF WHEN TYPING OR WASHING DISHES) ON ADVICE OF THERAPIST TO BEGIN TO STRENGTHEN WRIST AND DO THERAPEUTIC EXERCISES. I FEEL THE TEE PEE CONTRIBUTED TO THIS. IF THERE HAD BEEN EITHER A SHORTER PLASTIC STAY OR AN EXTENDED STAY LIKE IN THE THUMB/WRIST SPLINT, MY WRIST WOULD NOT HAVE BEEN INJURED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TEE PEE THUMB SUPPORT FYH MEDICAL SPECIALTIES 223084

Patients

Seq Age Sex Outcome Treatment
1 61 YR Required Intervention