SHARPS CONTAINER 8GAL RED 8997PG2

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-01-13 for SHARPS CONTAINER 8GAL RED 8997PG2 manufactured by Covidien.

Event Text Entries

[174704614] The complainant indicated that the device will not be returned for evaluation; 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. As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product. 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


[174704615] The customer reported that the white lids do not fit properly on the container.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1424643-2020-00563
MDR Report Key9580263
Report SourceUSER FACILITY
Date Received2020-01-13
Date of Report2020-01-15
Date of Event2019-12-15
Date Mfgr Received2019-12-16
Date Added to Maude2020-01-13
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 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 NameSHARPS CONTAINER 8GAL RED
Generic NameCONTAINER, SHARPS
Product CodeMMK
Date Received2020-01-13
Model Number8997PG2
Catalog Number8997PG2
Lot Number19F01563
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address815 TEK DRIVE CRYSTAL LAKE IL 600399002 US 600399002


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-13

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