FDA Adverse Event Death Summary report: N

SMART TIP SCISSORS

MDR report key: 23092 · Received June 1, 1995

Report

Report Number
2939738-1995-00001
Event Type
Death
Date Received
June 1, 1995
Report Date
June 1, 1995
Manufacturer
MARLOW SURGICAL TECHNOLOGIES, INC.
Product Code
LRW
Adverse Event
Yes
Report Source
Distributor report
Reporter Location
FR
Reporter Occupation
UNKNOWN

Narratives

Description of Event or Problem · 1

UNCLEAR AT THIS TIME.INVALID DATA - REGARDING SINGLE USE LABELING OF DEVICE. PATIENT MEDICAL STATUS PRIOR TO EVENT: INVALID DATA. THERE WAS NOT 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.INVALID DATA - REGARDING WHETHER EVENT PRESENTS IMMINENT HAZARD. INVALID DATA - WHETHER 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.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SMART TIP SCISSORS SCISSORS LRW MARLOW SURGICAL TECHNOLOGIES, INC. UNKNOWN UNKNOWN

Patients

Seq Age Sex Outcome Treatment
1 UNK Death