CONTAINER SHARPS RED SLIDE LID DISP 18GL 8938

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-05 for CONTAINER SHARPS RED SLIDE LID DISP 18GL 8938 manufactured by Covidien.

Event Text Entries

[182171030] The complainant indicated that the device will not be returned for evaluation as it has been discarded; therefore, a failure analysis is not available, and we are not able to determine the relationship between this device and the cause for this event.? If additional information or the sample is received, the investigation will be reopened and responded to accordingly.
Patient Sequence No: 1, Text Type: N, H10


[182171031] The customer reported that the container was cracked. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1424643-2020-00571
MDR Report Key9792897
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-05
Date of Report2020-03-05
Date of Event2020-03-02
Date Mfgr Received2020-03-02
Date Added to Maude2020-03-05
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 ContactJILL SARAIVA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5086183640
Manufacturer G1COVIDIEN
Manufacturer Street815 TEK DRIVE
Manufacturer CityCRYSTAL LAKE IL 600399002
Manufacturer CountryUS
Manufacturer Postal Code600399002
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONTAINER SHARPS RED SLIDE LID DISP 18GL
Generic NameCONTAINER, SHARPS
Product CodeMMK
Date Received2020-03-05
Model Number8938
Catalog Number8938
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address815 TEK DRIVE CRYSTAL LAKE IL 600399002 US 600399002


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-05

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