POOLE SUCTION INSTRUMENT 50/C 0035040

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2018-01-03 for POOLE SUCTION INSTRUMENT 50/C 0035040 manufactured by Conmed Corporation.

Event Text Entries

[96506271] The reported devices are expected to be returned for evaluation. A supplemental and final report will be filed upon the completion of the product evaluation and complaint investigation.
Patient Sequence No: 1, Text Type: N, H10


[96506272] The distributor in (b)(4) rejected two poole suction instrument 50/c for "insufficient heatseal" during incoming inspection. In this instance, there was no patient involvement as the packaging anomaly was discovered during inspection prior to distribution to an end-user. The report is raised on the basis of a device malfunction with potential for injury with recurrence.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1320894-2017-00292
MDR Report Key7159678
Report SourceDISTRIBUTOR,FOREIGN,OTHER
Date Received2018-01-03
Date of Report2018-02-14
Date Mfgr Received2018-02-13
Device Manufacturer Date2017-03-06
Date Added to Maude2018-01-03
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 13502
Manufacturer CountryUS
Manufacturer Postal13502
Manufacturer Phone7273995209
Manufacturer G1CONMED CORPORATION
Manufacturer Street525 FRENCH ROAD
Manufacturer CityUTICA NY 13502
Manufacturer CountryUS
Manufacturer Postal Code13502
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePOOLE SUCTION INSTRUMENT 50/C
Generic NameSURGICAL INSTRUMENTS, STERILE
Product CodeBYY
Date Received2018-01-03
Returned To Mfg2018-02-05
Catalog Number0035040
Lot Number201703061
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCONMED CORPORATION
Manufacturer Address525 FRENCH ROAD UTICA NY 13502 US 13502


Patients

Patient NumberTreatmentOutcomeDate
10 2018-01-03

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