AQUA-SEAL CDU 8888571299

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 2018-09-25 for AQUA-SEAL CDU 8888571299 manufactured by Covidien.

Event Text Entries

[121570065] Submitted september 25, 2018. 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


[121570066] The customer states there was no suction when they connected the chest drainage unit. Another unit was attached and there was no harm to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9611018-2018-00302
MDR Report Key7905130
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-09-25
Date of Report2018-09-25
Date of Event2018-08-24
Date Mfgr Received2018-09-11
Date Added to Maude2018-09-25
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 ContactEDWARD ALMEIDA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524151
Manufacturer G1COVIDIEIN
Manufacturer StreetSRAGH INDUSTRIAL ESTATE, CO, T
Manufacturer CityOFFALY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAQUA-SEAL CDU
Generic NameCHEST DRAINAGE KIT
Product CodePAD
Date Received2018-09-25
Model Number8888571299
Catalog Number8888571299
Lot Number17E079FHX
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressSRAGH INDUSTRIAL ESTATE, CO, T OFFALY EI


Patients

Patient NumberTreatmentOutcomeDate
10 2018-09-25

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