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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CareFusion, Inc SAFE-T-CENTESIS TRAY 6FR X 16CM; thoracentesis tray

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CareFusion, Inc SAFE-T-CENTESIS TRAY 6FR X 16CM; thoracentesis tray Back to Search Results
Catalog Number PIG1260T
Medical Device Problem Code Device Markings/Labelling Problem (2911)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 07/29/2026
Type of Reportable Event Malfunction
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Brand Name
SAFE-T-CENTESIS TRAY 6FR X 16CM
Common Device Name
thoracentesis tray
Manufacturer (Section D)
CareFusion, Inc
75 n. fairview drive
vernon hills IL 60061
Manufacturer (Section G)
Bard Reynosa S.A. de C.V. -9617592
blvd. montebello #1
parque industrial colonial
reynosa, tamaulipas 88780
MX   88780
Manufacturer Contact
michael gaffney
75 n. fairview drive
vernon hills, IL 60061
+1(801)565-2341
MDR Report Key50862899
Report Number1423507-2026-00289
Device Sequence Number18486622
Product Code PXI
UDI-Device Identifier10885403108365
UDI-Public(01)10885403108365(17)280430(10)RELP3029
Combination Product (Y/N)N
Initial Reporter StateNC
Initial Reporter CountryUS
PMA/510(K) Number
NA
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Company Representative
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 09/18/2026
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 Health Professional
Device Catalogue NumberPIG1260T
Device Lot NumberRELP3029
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/31/2026
Initial Report FDA Received Date09/22/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured03/19/2026
Is the Device Labeled for Single Use? (Y/N) Yes
Usage of Device Initial
Patient Sequence Number1
Patient SexUnknown
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