1/4"(6.4MM) X6'(1.8M) W/M&F CO 0037860

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 2017-09-13 for 1/4"(6.4MM) X6'(1.8M) W/M&F CO 0037860 manufactured by Consolidated Medical Equipment.

Event Text Entries

[86007968] The reported device 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


[86007969] The distributor in (b)(6) rejected one (b)(4) surgical tubing with "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 Number3007305485-2017-00208
MDR Report Key6862459
Report SourceDISTRIBUTOR,FOREIGN,OTHER
Date Received2017-09-13
Date of Report2017-11-06
Date Mfgr Received2017-11-01
Device Manufacturer Date2016-11-15
Date Added to Maude2017-09-13
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 ContactMRS. MARTHA CAMACHO URRIBARRI
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 Name1/4"(6.4MM) X6'(1.8M) W/M&F CO
Generic NameSURGICAL TUBING
Product CodeBYY
Date Received2017-09-13
Returned To Mfg2017-10-30
Catalog Number0037860
Lot Number201611154
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
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 2017-09-13

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