SINGLE FUNCTION HNDPC ABC ELEC 130344

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 2018-03-08 for SINGLE FUNCTION HNDPC ABC ELEC 130344 manufactured by Consolidated Medical Equipment.

Event Text Entries

[102126478] The reported unused device was returned for evaluation in its original unopened package. Label verification and visual inspection were performed. The complaint product was observed to have damage on the packaging's tyvek material. This damage caused a breach in sterility. Due to the extent and appearance of the damage on the outside of the tyvek material, it appears that the product packaging was damaged from the outside. It is likely that the package was damaged from an outside source and therefore not likely a manufacturing defect. The manufacturing documents from the device history record have been reviewed with special attention to the manufacturing and inspection of this product. The products released for distribution were found to have met all specifications prior to shipment. Of the lot containing 600 units, no prior complaints have been received. A two-year review of complaint history revealed two similar prior complaints. During this same time frame, 31,500 devices have been manufactured and shipped worldwide. A risk analysis was performed and deemed acceptable. This reported packaging issue was obvious to the distributor, prompting the return of the device for evaluation. There was no patient involvement. As with all medical devices, examination of the product occurs multiple times prior to use. Good clinical practice would include examination and verification of the original packaging and its labeling to ensure both are intact. The instructions for use (ifu) provides the following warning. -if packaging has been opened/damaged or altered, do not use the product and contact the manufacturer immediately. This issue will continue to be monitored through the complaint system to assure patient safety.
Patient Sequence No: 1, Text Type: N, H10


[102126479] The distributor in (b)(4) reported a "tear" on the sterile pouch of the device. There was no patient involvement as this defect was discovered during incoming inspection. This report is raised on the basis of a sterility breach found during the device evaluation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3007305485-2018-00061
MDR Report Key7323749
Report SourceDISTRIBUTOR,FOREIGN
Date Received2018-03-08
Date of Report2018-03-08
Date Mfgr Received2018-02-22
Device Manufacturer Date2017-01-02
Date Added to Maude2018-03-08
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 NameSINGLE FUNCTION HNDPC ABC ELEC
Generic NameABC HANDPIECES-OPEN
Product CodeHAM
Date Received2018-03-08
Returned To Mfg2017-10-02
Model Number130344
Catalog Number130344
Lot Number201701024
Device AvailabilityR
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 2018-03-08

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