ZIMMER UNK *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2005-02-17 for ZIMMER UNK * manufactured by Zimmer Pt Care Div.

Event Text Entries

[393791] When moving the pt's bed, the trapeze support broke causing it to fall and strike the pt's head.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW1034703
MDR Report Key575093
Date Received2005-02-17
Date of Report2005-02-17
Date of Event2005-02-14
Date Added to Maude2005-02-24
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA0
Report to FDA0
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameZIMMER
Generic NameTRAPEZE BAR
Product CodeILZ
Date Received2005-02-17
Model NumberUNK
Catalog Number*
Lot Number*
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key564940
ManufacturerZIMMER PT CARE DIV
Manufacturer Address1872 OLD MOUNTAIN RD. STATESVILLE NC 28677 US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-02-17

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