PANEL CLAMP UPPER AND LOWER * 640-013 AND 640-014

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2001-04-06 for PANEL CLAMP UPPER AND LOWER * 640-013 AND 640-014 manufactured by Zimmer Patient Care.

Event Text Entries

[198146] Patient pulled on trapeze and the panel clamps allegedly came loose with the overhead bar and the pulley/trapeze coming down and striking right arm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1035617-2001-00006
MDR Report Key327140
Report Source04
Date Received2001-04-06
Date of Report2001-02-23
Date of Event2001-02-21
Date Mfgr Received2001-03-12
Date Added to Maude2001-04-19
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactPAULA OSORIO
Manufacturer Street200 W. OHIO AVENUE
Manufacturer CityDOVER OH 44622
Manufacturer CountryUS
Manufacturer Postal44622
Manufacturer Phone3303438801
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePANEL CLAMP UPPER AND LOWER
Generic NamePANEL CLAMP
Product CodeHSQ
Date Received2001-04-06
Model Number*
Catalog Number640-013 AND 640-014
Lot NumberNA
ID Number*
OperatorLAY USER/PATIENT
Device AvailabilityY
Device AgeNO INFO
Device Eval'ed by MfgrY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key316536
ManufacturerZIMMER PATIENT CARE
Manufacturer Address2021 OLD MOUNTAIN RD. STATESVILLE NC 28677 US
Baseline Brand NamePANEL CLAMP UPPER AND LOWER
Baseline Generic NamePANEL CLAMP
Baseline Model No*
Baseline Catalog No640-013 AND 640-014
Baseline ID*


Patients

Patient NumberTreatmentOutcomeDate
10 2001-04-06

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.