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 |