ETHH12LP

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2016-10-06 for ETHH12LP manufactured by Sterilmed, Inc..

Event Text Entries

[56586525] The device has not yet been returned to the manufacturer at the time of this report. A supplemental form will be sent once the evaluation is completed if the device is returned. The device history report was not reviewed as no lot number was given.
Patient Sequence No: 1, Text Type: N, H10


[56586526] It was reported that the device fell apart in the middle of a case. Additional information was requested but no additional information or responses were received.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134070-2016-00072
MDR Report Key6003595
Report SourceHEALTH PROFESSIONAL
Date Received2016-10-06
Date of Report2016-09-08
Date of Event2016-06-29
Date Mfgr Received2016-09-08
Date Added to Maude2016-10-06
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJASON ANDERSON
Manufacturer Street5010 CHESHIRE PARKWAY SUITE 2
Manufacturer CityPLYMOUTH MN 55446
Manufacturer CountryUS
Manufacturer Postal55446
Manufacturer Phone7634888348
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Generic NameLAPAROSCOPE, GENERAL & PLASTIC SURGERY, REPROCESSED
Product CodeNLM
Date Received2016-10-06
Model NumberETHH12LP
Catalog NumberETHH12LP
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTERILMED, INC.
Manufacturer Address11400 73RD AVE N MAPLE GROVE MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2016-10-06

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