POOLE SUCTION SURGICAL INSTRUMENT 0035040

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2017-06-27 for POOLE SUCTION SURGICAL INSTRUMENT 0035040 manufactured by Conmed Corporation.

Event Text Entries

[78594643] The reported 0035040- poole suction instrument is expected to be returned for evaluation. A supplemental and final report will be filed upon the completion of the product evaluation and the complaint investigation.
Patient Sequence No: 1, Text Type: N, H10


[78594644] The distributor in (b)(6) reported that during inspection of incoming products, one poole suction instrument was discovered with "insufficient heatseal". In this instance, there was no patient involvement as the packaging anomaly was discovered during inspection prior to distribution to an end-user.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1320894-2017-00154
MDR Report Key6671957
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2017-06-27
Date of Report2017-09-18
Date of Event2017-05-30
Date Mfgr Received2017-09-15
Device Manufacturer Date2016-07-26
Date Added to Maude2017-06-27
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 ContactMS. LINDSEY SHEPPARD
Manufacturer Street525 FRENCH ROAD
Manufacturer CityUTICA NY 135025994
Manufacturer CountryUS
Manufacturer Postal135025994
Manufacturer Phone7273995209
Manufacturer G1CONMED CORPORATION
Manufacturer Street525 FRENCH ROAD
Manufacturer CityUTICA NY 135025994
Manufacturer CountryUS
Manufacturer Postal Code135025994
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePOOLE SUCTION SURGICAL INSTRUMENT
Generic NamePOOLE SUCTION TUBING
Product CodeBYY
Date Received2017-06-27
Returned To Mfg2017-08-14
Catalog Number0035040
Lot Number201607261
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCONMED CORPORATION
Manufacturer Address525 FRENCH ROAD UTICA NY 135025994 US 135025994


Patients

Patient NumberTreatmentOutcomeDate
10 2017-06-27

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