NOZZLE,STRAIGHT,ABC,DISP/20 130343

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2018-01-03 for NOZZLE,STRAIGHT,ABC,DISP/20 130343 manufactured by Consolidated Medical Equipment.

Event Text Entries

[96232557] 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


[96232558] The distributor in (b)(4) rejected 40 abc nozzles 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 Number3007305485-2017-00291
MDR Report Key7159684
Report SourceDISTRIBUTOR,FOREIGN
Date Received2018-01-03
Date of Report2018-02-12
Date Mfgr Received2017-12-12
Device Manufacturer Date2017-03-29
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 NameNOZZLE,STRAIGHT,ABC,DISP/20
Generic NameABC HANDPIECES-OPEN
Product CodeHAM
Date Received2018-01-03
Catalog Number130343
Lot Number201703294
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCONSOLIDATED MEDICAL EQUIPMENT
Manufacturer AddressAVE. ALEJANDRO DUMAS NO. 11321 COMPLEJO INDUSTRIAL CHIHUAHUA CHIHUAHUA, CHIHUAHUA 31136 MX 31136


Patients

Patient NumberTreatmentOutcomeDate
10 2018-01-03

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