LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET G23747 LR-EVN-13.0-RL

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 2020-03-17 for LEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET G23747 LR-EVN-13.0-RL manufactured by Cook Vandergrift Inc.

MAUDE Entry Details

Report Number2522007-2020-00012
MDR Report Key9842062
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-17
Date of Report2020-03-16
Date of Event2020-02-17
Device Manufacturer Date2019-10-28
Date Added to Maude2020-03-17
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 ContactMR. BRIAN JOHNSTON
Manufacturer Street1186 MONTGOMERY LANE
Manufacturer CityVANDERGRIFT PA 15690
Manufacturer CountryUS
Manufacturer Postal15690
Manufacturer Phone7248458621
Manufacturer G1COOK VANDERGRIFT INC
Manufacturer Street1186 MONTGOMERY LANE
Manufacturer CityVANDERGRIFT PA 15690
Manufacturer CountryUS
Manufacturer Postal Code15690
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLEAD EXTRACTION EVOLUTION RL CONTROLLED-ROTATION DILATOR SHEATH SET
Generic NameVESSEL DILATOR FOR PERCUTANEOUS CATHETERIZATION
Product CodeDRE
Date Received2020-03-17
Model NumberG23747
Catalog NumberLR-EVN-13.0-RL
Lot NumberN167520
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOOK VANDERGRIFT INC
Manufacturer Address1186 MONTGOMERY LANE VANDERGRIFT PA 15690 US 15690


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-17

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