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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: AVID MEDICAL, INC. AVID TRUCUSTOM; GENERAL SURGERY TRAY

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AVID MEDICAL, INC. AVID TRUCUSTOM; GENERAL SURGERY TRAY Back to Search Results
Catalog Number CHWE011-01
Device Problem Device Contaminated During Manufacture or Shipping (2969)
Patient Problem Insufficient Information (4580)
Event Date 07/23/2021
Event Type  malfunction  
Event Description
A human hair was found inside the basin set of an avid trucustom general surgical procedure kit when opened for an orif of the ankle.As a result, another general surgical procedure kit needed to be open to continue with the surgical procedure.
 
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Brand Name
AVID TRUCUSTOM
Type of Device
GENERAL SURGERY TRAY
Manufacturer (Section D)
AVID MEDICAL, INC.
9000 westmont dr
stonehouse commerce park
toano VA 23168
MDR Report Key12452566
MDR Text Key270786652
Report Number12452566
Device Sequence Number1
Product Code LRO
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source User Facility
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 08/26/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/10/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator No Information
Device Catalogue NumberCHWE011-01
Device Lot Number1453091
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA08/26/2021
Event Location Hospital
Date Report to Manufacturer09/10/2021
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
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