1180501106 SCOTSMAN YANKAUER REG X100

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 2020-03-20 for 1180501106 SCOTSMAN YANKAUER REG X100 manufactured by Covidien.

Event Text Entries

[184630329] The incident sample has been requested but to date has not been received for evaluation. If the sample is received, or if additional information pertinent to the incident is obtained a follow-up report will be submitted. As part of our manufacturing process, all device history records are reviewed and approved by quality, prior to release of product.
Patient Sequence No: 1, Text Type: N, H10


[184630330] The customer reported that the green rubber end of the yankauer catheter became loose and dislodged during oral suction. The green rubber was pulled back into the catheter resulting in a blockage. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611018-2020-00422
MDR Report Key9859496
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-20
Date of Report2020-03-20
Date of Event2020-02-27
Date Mfgr Received2020-03-11
Date Added to Maude2020-03-20
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 StreetSRAGH INDUSTRIAL ESTATE, CO, T
Manufacturer CityOFFALY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand Name1180501106 SCOTSMAN YANKAUER REG X100
Generic NameAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED
Product CodeGCX
Date Received2020-03-20
Model Number1180501106
Catalog Number1180501106
Lot Number18F026FHX
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressSRAGH INDUSTRIAL ESTATE, CO, T OFFALY EI


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-20

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