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.
[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
Report Number | 9612030-2019-02171 |
MDR Report Key | 8603413 |
Date Received | 2019-05-13 |
Date of Report | 2019-11-11 |
Date of Event | 2019-02-18 |
Date Mfgr Received | 2019-04-23 |
Date Added to Maude | 2019-05-13 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | JILL SARAIVA |
Manufacturer Street | 15 HAMPSHIRE STREET |
Manufacturer City | MANSFIELD MA 02048 |
Manufacturer Country | US |
Manufacturer Postal | 02048 |
Manufacturer Phone | 5084524970 |
Manufacturer G1 | COVIDIEN |
Manufacturer Street | CALLE 9 SUR NO. 125 CUIDAD IND |
Manufacturer City | TIJUANA 22500 |
Manufacturer Country | MX |
Manufacturer Postal Code | 22500 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SALEM SUMP W/ ARV 16FR. 48IN |
Generic Name | TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUBATION |
Product Code | FEG |
Date Received | 2019-05-13 |
Model Number | 8888266130 |
Catalog Number | 8888266130 |
Lot Number | 1824500364 |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COVIDIEN |
Manufacturer Address | CALLE 9 SUR NO. 125 CUIDAD IND TIJUANA 22500 MX 22500 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-05-13 |