SALEM SUMP W/ ARV 16FR. 48IN 8888266130

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-05-13 for SALEM SUMP W/ ARV 16FR. 48IN 8888266130 manufactured by Covidien.

Event Text Entries

[145232273] 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


[145232274] The customer reported that there was a cut or indent on the entry site of the connection causing the feed to leak. The tube was removed and replaced with no harm to the patient. Prior to insertion of the second tube, the health care provider noticed this same issue on two other tubes in the same spot on the device and did not use them.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9612030-2019-02171
MDR Report Key8603413
Date Received2019-05-13
Date of Report2019-11-11
Date of Event2019-02-18
Date Mfgr Received2019-04-23
Date Added to Maude2019-05-13
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 Phone5084524970
Manufacturer G1COVIDIEN
Manufacturer StreetCALLE 9 SUR NO. 125 CUIDAD IND
Manufacturer CityTIJUANA 22500
Manufacturer CountryMX
Manufacturer Postal Code22500
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSALEM SUMP W/ ARV 16FR. 48IN
Generic NameTUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION
Product CodeFEG
Date Received2019-05-13
Model Number8888266130
Catalog Number8888266130
Lot Number1824500364
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer AddressCALLE 9 SUR NO. 125 CUIDAD IND TIJUANA 22500 MX 22500


Patients

Patient NumberTreatmentOutcomeDate
10 2019-05-13

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