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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BENCHMARK ZOOM LATITUDE; EXTERNAL PROGRAMMER

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BENCHMARK ZOOM LATITUDE; EXTERNAL PROGRAMMER Back to Search Results
Model Number 3120
Medical Device Problem Code Power Problem (3010)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 04/26/2021
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
 
Event or Problem Description
It was reported that the programmer socket was burned out and did not turn on.Furthermore, the programmer will be replaced and returned for repair/analysis.No patient involvement was reported.
 
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Brand Name
ZOOM LATITUDE
Common Device Name
EXTERNAL PROGRAMMER
Manufacturer (Section D)
BENCHMARK
4065 theurer boulevard
winona MN 55987
MDR Report Key12071946
Report Number2124215-2021-11884
Device Sequence Number10987380
Product Code LWS
UDI-Device Identifier00802526564703
UDI-Public00802526564703
Combination Product (Y/N)N
Initial Reporter CountryIT
PMA/510(K) Number
P910077/S046
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)Unknown
Reporter Type Manufacturer
Report Source health professional
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 06/25/2021
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 Number3120
Device Catalogue Number3120
Device Lot Number062992
Was Device Available for Evaluation? No
Type of Report(Section G)Initial
Initial Date Received by Manufacturer 04/26/2021
Initial Report FDA Received Date06/25/2021
Patient Sequence Number1
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