MAYO TABLE 0617769000 *

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2007-06-19 for MAYO TABLE 0617769000 * manufactured by Blickman, Inc..

Event Text Entries

[623220] Mayo table doesn't stay in place and slides down by itself.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number881504
MDR Report Key881504
Date Received2007-06-19
Date of Report2007-06-19
Date of Event2007-06-18
Report Date2007-06-19
Date Reported to FDA2007-06-19
Date Added to Maude2007-07-18
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameMAYO TABLE
Generic NameTABLE
Product CodeLDQ
Date Received2007-06-19
Model Number0617769000
Catalog Number*
Lot Number*
ID Number*
Device AvailabilityY
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key860154
ManufacturerBLICKMAN, INC.
Manufacturer Address39 ROBINSON RD LODI NJ 07644 US


Patients

Patient NumberTreatmentOutcomeDate
10 2007-06-19

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