MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2006-11-16 for TCI- TUMESCENT CATHETER INVERSION SYSTEM 7210023 * manufactured by Smith & Nephew Inc. - Endoscopy Division.
[556695]
During a vein stripping procedure, the green tip on the catheter came off during pull back and was left inside the patient's mid-thigh. Customer states cannot see it on x-ray. There was a one-hour delay reported.
Patient Sequence No: 1, Text Type: D, B5
[7806773]
Device has not been returned for evaluation, therefore, no determination could be made for the reported device failure.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1216828-2006-00049 |
MDR Report Key | 788383 |
Report Source | 06,07 |
Date Received | 2006-11-16 |
Date of Report | 2006-11-14 |
Date of Event | 2006-10-16 |
Date Facility Aware | 2006-10-16 |
Report Date | 2006-11-14 |
Date Mfgr Received | 2006-10-16 |
Device Manufacturer Date | 2006-03-01 |
Date Added to Maude | 2006-12-04 |
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 | DONNA LANTEIGNE |
Manufacturer Street | 150 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal | 01810 |
Manufacturer Phone | 9787491576 |
Manufacturer G1 | SMITH & NEPHEW, INC. |
Manufacturer Street | 160 DASCOMB ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal Code | 01810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TCI- TUMESCENT CATHETER INVERSION SYSTEM |
Generic Name | * |
Product Code | GAJ |
Date Received | 2006-11-16 |
Model Number | 7210023 |
Catalog Number | * |
Lot Number | 60830728 |
ID Number | * |
Device Expiration Date | 2008-12-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | 7 MO |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 776095 |
Manufacturer | SMITH & NEPHEW INC. - ENDOSCOPY DIVISION |
Manufacturer Address | * ANDOVER MA * US |
Baseline Brand Name | TCI TUMESCENT CATHETER INVERSION SYSTEM |
Baseline Generic Name | * |
Baseline Model No | 7210023 |
Baseline Catalog No | * |
Baseline ID | * |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2006-11-16 |