ETHCB12LT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2016-09-15 for ETHCB12LT manufactured by Sterilmed, Inc..

Event Text Entries

[54794014] 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 unable to be reviewed as no lot number was given.
Patient Sequence No: 1, Text Type: N, H10


[54794015] It was reported that the device broke into 4 pieces, none into patient cavity but it did brake apart while inside patient. The cap, seal, and knob just fell apart. No patient injury or consequences were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134070-2016-00066
MDR Report Key5952657
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2016-09-15
Date of Report2016-08-23
Date of Event2016-08-23
Date Mfgr Received2016-08-23
Date Added to Maude2016-09-15
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 200
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 Received2016-09-15
Model NumberETHCB12LT
Catalog NumberETHCB12LT
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 2016-09-15

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