ZIMMER 3820 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2000-08-25 for ZIMMER 3820 * manufactured by Zimmer, Inc. Patient Care Div..

Event Text Entries

[186089] Cast cart turned over on employee.
Patient Sequence No: 1, Text Type: D, B5

MAUDE Entry Details

• Report Number: MW1019807
• MDR Report Key: 292997
• Date Received: 2000-08-25
• Date of Report: 2000-08-25
• Date of Event: 2000-08-18
• Date Added to Maude: 2000-08-30
• Event Key: 0
• Report Source Code: Voluntary report
• Manufacturer Link: N
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 0
• Health Professional: 3
• Initial Report to FDA: 0
• Report to FDA: 0
• Event Location: 3
• Single Use: 0
• Previous Use Code: 0
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: ZIMMER
• Generic Name: CAST CART
• Product Code: LFG
• Date Received: 2000-08-25
• Model Number: 3820
• Catalog Number: *
• Lot Number: *
• ID Number: *
• Operator: HEALTH PROFESSIONAL
• Device Availability: Y
• Implant Flag: N
• Date Removed: *
• Device Sequence No: 1
• Device Event Key: 283596
• Manufacturer: ZIMMER, INC. PATIENT CARE DIV.
• Manufacturer Address: 200 W OHIO AVE. DOVER OH 44622 US
• Baseline Brand Name: ZIMMER CAST CART
• Baseline Generic Name: CAST CART
• Baseline Model No: NA
• Baseline Catalog No: 3820
• Baseline ID: NA
• Baseline Device Family: NA
• Baseline Shelf Life [Months]: NA
• Baseline PMA Flag: N
• Baseline 510K PMN: N
• Baseline Preamendment: N
• Baseline Transitional: N
• 510k Exempt: Y

Patients

Patient Number	Treatment	Outcome	Date
1	0	1. Other	2000-08-25