450 SAL EJECTOR 3283 8881450004

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2009-08-21 for 450 SAL EJECTOR 3283 8881450004 manufactured by Covidien.

Event Text Entries

[1234426] It was reported to covidien on 08/14/2009 that a customer had an issue with a saliva ejector. The customer states the tip fell off in a pt's mouth.
Patient Sequence No: 1, Text Type: D, B5


[8420706] (b) (4). An investigation is currently underway. Upon completion, the results will be forwarded.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9612030-2009-00025
MDR Report Key1493979
Report Source05,06
Date Received2009-08-21
Date of Report2009-08-14
Report Date2009-08-14
Date Reported to Mfgr2009-08-14
Date Mfgr Received2009-08-14
Date Added to Maude2009-11-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location3
Manufacturer ContactELAINE BISHOP
Manufacturer Street15 HAMPSHIRE ST
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524686
Manufacturer G1COVIDIEN
Manufacturer StreetCALLE 9 SUR NO. 125 CUIDAD INDUSTRIAL
Manufacturer CityTIJUANA 92173
Manufacturer CountryMX
Manufacturer Postal Code92173
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name450 SAL EJECTOR 3283
Generic NameSALIVA EJECTOR
Product CodeDYN
Date Received2009-08-21
Returned To Mfg2009-07-16
Model Number8881450004
Catalog Number8881450004
Lot Number900703264
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressCALLE 9 SUR NO. 125 CUID TIJUANA 92173 MX 92173


Patients

Patient NumberTreatmentOutcomeDate
10 2009-08-21

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