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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BAXTER HEALTHCARE CORPORATION Novum IQ; Pump, infusion

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BAXTER HEALTHCARE CORPORATION Novum IQ; Pump, infusion Back to Search Results
Model Number 40700BAXUS
Medical Device Problem Code Filling Problem (1233)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event Malfunction
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Brand Name
Novum IQ
Common Device Name
Pump, infusion
Manufacturer (Section D)
BAXTER HEALTHCARE CORPORATION
deerfield IL
Manufacturer (Section G)
ORBRAY THAILAND CO., LTD.
northern region ind. estate
60/29 moo 4, tambol banklang
a.muang, ban klang, lamphun NA 51000
TH   51000
Manufacturer Contact
25212 w. illinois route 120
round lake, IL 60073
+1(224)270-5355
MDR Report Key50849271
Report Number1416980-2026-02995
Device Sequence Number9936371
Product Code FRN
UDI-Device Identifier05413765851797
UDI-Public(01)05413765851797
Combination Product (Y/N)N
Initial Reporter StateVA
Initial Reporter CountryUS
PMA/510(K) Number
K211122
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional,Company Representative
Initial Reporter Occupation Biomedical Engineer
Type of Report Initial
Report Date (Section B) 09/21/2026
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 Model Number40700BAXUS
Device Catalogue Number40700BAXUS
Device Lot NumberN/A
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer09/03/2026
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/25/2026
Initial Report FDA Received Date09/21/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
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