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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CARDINAL HEALTH 200, LLC C-SECTION PACK; CESAREAN SECTION TRAY

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CARDINAL HEALTH 200, LLC C-SECTION PACK; CESAREAN SECTION TRAY Back to Search Results
Model Number SMA4ECSHTB
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 02/12/2024
Event Type  malfunction  
Event Description
There was a fuzzy piece of lint on a towel.
 
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Brand Name
C-SECTION PACK
Type of Device
CESAREAN SECTION TRAY
Manufacturer (Section D)
CARDINAL HEALTH 200, LLC
MDR Report Key18798305
MDR Text Key336546608
Report NumberMW5152056
Device Sequence Number1
Product Code OHM
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 02/13/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model NumberSMA4ECSHTB
Device Catalogue NumberSMA4ECSHTB
Device Lot Number141711
Was Device Available for Evaluation? No
Initial Date Manufacturer Received Not provided
Initial Date FDA Received02/27/2024
Patient Sequence Number1
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