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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ICU Medical Healthcare Manufacturing S.A. de C.V. Deltec Gripper Plus Needles; Set, administration, intravascular

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ICU Medical Healthcare Manufacturing S.A. de C.V. Deltec Gripper Plus Needles; Set, administration, intravascular Back to Search Results
Catalog Number 21-3468-24
Medical Device Problem Code Obstruction of Flow (2423)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/12/2026
Type of Reportable Event Malfunction
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Brand Name
Deltec Gripper Plus Needles
Common Device Name
Set, administration, intravascular
Manufacturer (Section D)
ICU Medical Healthcare Manufacturing S.A. de C.V.
ave calidad no. 4, parque
tijuana NA 22425
MX  22425
Manufacturer Contact
reed covert
951 calle amanecer
san clemente, CA 92673
+1(224)706-2300
MDR Report Key50652286
Report Number9617604-2026-00563
Device Sequence Number9717692
Product Code FPA
UDI-Device Identifier10610586033070
UDI-Public(01)10610586033070(17)310127(10)6170718
Combination Product (Y/N)N
Initial Reporter StateNA
Initial Reporter CountrySP
PMA/510(K) Number
K072657
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,User Facility
Initial Reporter Occupation Nurse
Type of Report Initial
Report Date (Section B) 09/07/2026
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 Number21-3468-24
Device Lot Number6170718
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 08/12/2026
Initial Report FDA Received Date09/07/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured01/28/2026
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 Initial
Patient Sequence Number1
Patient SexUnknown
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