FDA Adverse Event Other Summary report: N

COMFORT COOL THUMB CMC RESTRICTION SPLINT

MDR report key: 2249644 · Received August 26, 2011

Report

Report Number
2939821-2011-00012
Event Type
Other
Date Received
August 26, 2011
Report Date
August 24, 2011
Manufacturer
SCOTT SPECIALITIES, INC.
Product Code
ILH
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

NA.

Description of Event or Problem · 1

PATIENT DEVELOPED DERMATITIS AND A RASH AFTER WEARING THE THUMB CMC RESTRICTION SPLINT. THE SPLINT IS A LATEX FREE PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COMFORT COOL THUMB CMC RESTRICTION SPLINT THUMB CMC RESTRICTION SPLINT ILH SCOTT SPECIALITIES, INC. NA NA

Patients

Seq Age Sex Outcome Treatment
1 UNK Other