T REUTER BOBBIN W/ MICRON FINISH [ORIG ITEM: 145215] (6/PK) 145215-ENT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-02 for T REUTER BOBBIN W/ MICRON FINISH [ORIG ITEM: 145215] (6/PK) 145215-ENT manufactured by Gyrus Acmi, Inc.

Event Text Entries

[144133656] The device was not returned to olympus for evaluation. The cause of the reported event can be attributed to user error as the facility used the device after the expiration date printed on the product label.
Patient Sequence No: 1, Text Type: N, H10


[144133657] Olympus was informed that during an unknown procedure, an expired micron bobbin ventilation tube was placed in a patient. There was no patient injury reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2951238-2019-00798
MDR Report Key8576211
Date Received2019-05-02
Date of Report2019-05-02
Date of Event2019-03-01
Date Mfgr Received2019-04-10
Date Added to Maude2019-05-02
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. CONNIE TUBERA
Manufacturer Street2400 RINGWOOD AVENUE
Manufacturer CitySAN JOSE CA 95131
Manufacturer CountryUS
Manufacturer Postal95131
Manufacturer Phone4089355124
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameT REUTER BOBBIN W/ MICRON FINISH [ORIG ITEM: 145215] (6/PK)
Generic NameT REUTER BOBBIN W/ MICRON
Product CodeETD
Date Received2019-05-02
Model Number145215-ENT
Lot Number0913375098
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerGYRUS ACMI, INC
Manufacturer Address136 TURNPIKE ROAD SOUTHBOROUGH MA 01772 US 01772


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-02

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