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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PHILIPS NORTH AMERICA LLC FETAL SPIRAL ELECTRODE
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PHILIPS NORTH AMERICA LLC FETAL SPIRAL ELECTRODE Back to Search Results
Model Number FETAL SPIRAL ELECTRODE
Medical Device Problem Code Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code Post Operative Wound Infection (2446)
Date of Event 05/17/2021
Type of Reportable Event Serious Injury
Additional Manufacturer Narrative
This supplemental report is created with reference to mfg report #1218950-2021-11146 with corrected information to update the registered legal manufacturing site.
 
Event or Problem Description
It was reported to philips that the scalp electrode used for fetal monitoring caused a wound and possible infection and scars.
 
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Brand Name
FETAL SPIRAL ELECTRODE
Common Device Name
FETAL SPIRAL ELECTRODE
Manufacturer (Section D)
PHILIPS NORTH AMERICA LLC
3000 minuteman road
andover MA 01810
Manufacturer (Section G)
PHILIPS NORTH AMERICA LLC
3000 minuteman road
andover MA 01810
Manufacturer Contact
tara mackinnon
222 jacobs st
cambridge, MA 02141
6172455900
MDR Report Key13822648
Report Number1218950-2022-00225
Device Sequence Number2059040
Product Code HGP
UDI-Device Identifier20884838007431
UDI-Public20884838007431
Combination Product (Y/N)N
Initial Reporter CountrySW
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Initial Reporter Occupation Other
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Model NumberFETAL SPIRAL ELECTRODE
Device Catalogue Number989803137631
Device Lot NumberUNKNOWN
Was Device Available for Evaluation? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date03/19/2022
Usage of Device A
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
Patient SexUnknown
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