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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONVATEC INC L3C0600 - CURE PRODUCTS

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CONVATEC INC L3C0600 - CURE PRODUCTS Back to Search Results
Model Number 510852
Medical Device Problem Code Unsealed Device Packaging (1444)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event Malfunction
Event or Problem Description
It was reported "one catheter from each market unit with the individual package opened.End user did not use the opened product.He discarded them." each market unit was sealed upon receipt.No lot number information was provided.
 
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Brand Name
L3C0600 - CURE PRODUCTS
Manufacturer (Section D)
CONVATEC INC
211 american avenue
greensboro NC
Manufacturer (Section G)
CONVATEC INC
211 american avenue
greensboro NC
Manufacturer Contact
pamela meadows
7815 national service road
suite 600
greensboro, NC 
3365424679
MDR Report Key13894324
Report Number1049092-2022-00090
Device Sequence Number16572496
Product Code EZD
UDI-Device Identifier00815947020031
UDI-Public00815947020031
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
K132500
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Consumer,Distributor
Initial Reporter Occupation Other
Type of Report Initial
Report Date (Section B) 03/21/2022
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
Operator of Device Lay User/Patient
Device Model Number510852
Was Device Available for Evaluation? No
Was the Report Sent to FDA? No
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 03/21/2022
Initial Report FDA Received Date03/24/2022
Was Device Evaluated by Manufacturer? (Y/N) No
Is the Device Labeled for Single Use? (Y/N) Yes
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Unknown
Patient Sequence Number1
Patient SexMale
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