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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PHILIPS NORTH AMERICA LLC FR3 DEFIB, ECG UK ENGLISH (T) EXCHANGE; AED

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PHILIPS NORTH AMERICA LLC FR3 DEFIB, ECG UK ENGLISH (T) EXCHANGE; AED Back to Search Results
Model Number 861389
Device Problem Premature Discharge of Battery (1057)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
It has been reported that the device may be prematurely draining batteries.
 
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Brand Name
FR3 DEFIB, ECG UK ENGLISH (T) EXCHANGE
Type of Device
AED
Manufacturer (Section D)
PHILIPS NORTH AMERICA LLC
22100 bothell everett highway
bothell WA 98021
Manufacturer (Section G)
PHILIPS NORTH AMERICA LLC
22100 bothell everett highway
bothell WA 98021
Manufacturer Contact
shannon decker
22100 bothell everett highway
bothell, WA 98021
9095703538
MDR Report Key12455240
MDR Text Key270995051
Report Number3030677-2021-14227
Device Sequence Number1
Product Code MKJ
UDI-Device Identifier00884838049994
UDI-Public00884838049994
Combination Product (y/n)N
Reporter Country CodeAS
PMA/PMN Number
P160028
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor,foreign
Reporter Occupation Other
Type of Report Initial,Followup
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
Device Operator Other
Device Model Number861389
Device Catalogue Number453564405921
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Distributor Facility Aware Date08/16/2021
Initial Date Manufacturer Received 08/16/2021
Initial Date FDA Received09/10/2021
Supplement Dates Manufacturer Received11/01/2021
Supplement Dates FDA Received11/02/2021
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured07/01/2018
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
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