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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDLINE INDUSTRIES LP; 1LYRTR 16FR10ML100% SILTMP SNPOHR

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MEDLINE INDUSTRIES LP; 1LYRTR 16FR10ML100% SILTMP SNPOHR Back to Search Results
Catalog Number URO175816T
Device Problem Material Puncture/Hole (1504)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 08/08/2023
Event Type  malfunction  
Event Description
"urinary catheter bag with 2 holes and leaking urine ".
 
Manufacturer Narrative
It was reported by the customer that on (b)(6) 2023 "urinary catheter bag with 2 holes and leaking urine ".Due to this, the foley catheter was replaced.A sample was requested to be returned for evaluation.It has been determined that the reported event could cause or contribute to serious injury if it were to occur.In an abundance of caution, this medwatch is being filed.If any further relevant information is identified or obtained, a supplemental medwatch will be submitted.
 
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Type of Device
1LYRTR 16FR10ML100% SILTMP SNPOHR
Manufacturer (Section D)
MEDLINE INDUSTRIES LP
three lakes drive
northfield IL 60093
Manufacturer Contact
kelly zampella
three lakes drive
northfield, IL 60093
MDR Report Key17738236
MDR Text Key323685964
Report Number1417592-2023-00372
Device Sequence Number1
Product Code OHR
UDI-Device Identifier10193489988505
UDI-Public10193489988505
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Other
Type of Report Initial
Report Date 09/13/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/13/2023
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Catalogue NumberURO175816T
Was Device Available for Evaluation? No
Date Manufacturer Received08/18/2023
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
Patient Outcome(s) Other;
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