inforMED
InjuryIPG

BUNNYLINE

Received Dec 11, 1992 · Event occurred Jul 31, 1992

Report 3552 · MDR key 3552

Device

Generic name

Bunny Boot

Manufacturer

Dillon Orthopedics

Catalog number

05001-01

Narrative

Description of Event or Problem

THE BUNNY BOOT WAS APPLIED TO PREVENT FOOT DROP. PATIENT DEVELOPED NUMEROUS DARK BLUE LESIONS ON ONE HEEL AND AN ERTHEMATOUS AREA ON THE OTHERDEVICE LABELED FOR SINGLE USE. PATIENT MEDICAL STATUS PRIOR TO EVENT: INVALID DATA. INVALID DATA - REGARDING MULTIPLE PATIENT INVOLVEMENT.INVALID DATA - ON DEVICE SERVICE/MAINTENANCE. NO DATA - REGARDING DATE LAST SERVICED. SERVICE PROVIDED BY: INVALID DATA. INVALID DATA - SERVICE RECORDS AVAILABILITY. NO IMMINENT HAZARD TO PUBLIC HEALTH CLAIMED. DEVICE USED AS LABELED/INTENDED.INVALID DATA - REGARDING EVALUATION BY USER AFTER EVENT. METHOD OF EVALUATION: INVALID DATA. RESULTS OF EVALUATION: INVALID DATA. CONCLUSION: INVALID DATA. CERTAINTY OF DEVICE AS CAUSE OF OR CONTRIBUTOR TO EVENT: INVALID DATA. CORRECTIVE ACTIONS: NO DATA. INVALID DATA - ON DEVICE DESTROYED/DISPOSED OF STATUS.