MAUDE Adverse Event Report: BECTON, DICKINSON AND COMPANY / CAREFUSION 2200, INC. SNOWDEN PENCER; SCISSORS, GENERAL, SURGICAL

Lot Number 70637

Device Problem Difficult to Open or Close (2921)

Patient Problem Insufficient Information (4580)

Event Date 07/04/2020

Event Type  malfunction  

Event Description

Scissor tip would not open.Fda safety report id # (b)(4).

• Brand Name: SNOWDEN PENCER
• Type of Device: SCISSORS, GENERAL, SURGICAL
• Manufacturer (Section D): BECTON, DICKINSON AND COMPANY / CAREFUSION 2200, INC.
• MDR Report Key: 11207410
• MDR Text Key: 228442463
• Report Number: MW5098908
• Device Sequence Number: 1
• Product Code: LRW
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Risk Manager
• Type of Report: Initial
• Report Date: 01/15/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/20/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 09/01/2022
• Device Lot Number: 70637
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was Device Evaluated by Manufacturer?: No Information
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Age: 69 YR