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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDLINE INDUSTRIES, INC. BASIC ORTHO TRAY; ORTHOPEDIC TRAY

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MEDLINE INDUSTRIES, INC. BASIC ORTHO TRAY; ORTHOPEDIC TRAY Back to Search Results
Model Number DYNJ49369
Device Problem Manufacturing, Packaging or Shipping Problem (2975)
Patient Problem Insufficient Information (4580)
Event Date 08/20/2021
Event Type  malfunction  
Event Description
Medline basic ortho tray pack lap sponges contained an extra sponge (6 vs 5) which if not caught can alter correct sponge counts.Medline lap sponges mds252512lf, lot: 84321040049.Fda safety report id# (b)(4).
 
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Brand Name
BASIC ORTHO TRAY
Type of Device
ORTHOPEDIC TRAY
Manufacturer (Section D)
MEDLINE INDUSTRIES, INC.
MDR Report Key12365750
MDR Text Key268305901
Report NumberMW5103487
Device Sequence Number1
Product Code OJH
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Nurse
Type of Report Initial
Report Date 08/23/2021
2 Devices were Involved in the Event: 1   2  
1 Patient was Involved in the Event
Date FDA Received08/24/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Expiration Date04/30/2023
Device Model NumberDYNJ49369
Device Catalogue NumberDYNJ49369
Device Lot Number21FBM185
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Was Device Evaluated by Manufacturer? No Information
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
Patient Age68 YR
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