MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2002-08-13 for CODMAN DISPOSABLE VEIN STRIPPER 63-4031 manufactured by Codman & Shurtleff, Inc..
[261455]
The olive portion of the vein stripper became dislodged from cable during stripping of a vein. An add'l incision was required to remove the separated olive portion.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1226348-2002-00153 |
MDR Report Key | 409856 |
Report Source | 05,06 |
Date Received | 2002-08-13 |
Date of Report | 2002-07-22 |
Date of Event | 2002-07-22 |
Date Mfgr Received | 2002-07-22 |
Device Manufacturer Date | 2001-07-01 |
Date Added to Maude | 2002-08-14 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | MATTHEW KING |
Manufacturer Street | 325 PARAMOUNT DRIVE |
Manufacturer City | RAYNHAM MA 02767 |
Manufacturer Country | US |
Manufacturer Postal | 02767 |
Manufacturer Phone | 5088283106 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CODMAN DISPOSABLE VEIN STRIPPER |
Generic Name | STRIPPER, VEIN, DISPOSABLE |
Product Code | GAJ |
Date Received | 2002-08-13 |
Returned To Mfg | 2002-08-12 |
Model Number | NA |
Catalog Number | 63-4031 |
Lot Number | GT487 |
ID Number | NA |
Device Expiration Date | 2006-07-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 398869 |
Manufacturer | CODMAN & SHURTLEFF, INC. |
Manufacturer Address | 325 PARAMOUNT DRIVE RAYNHAM MA 02324 US |
Baseline Brand Name | CODMAN DISPOSABLE VEIN STRIPPER |
Baseline Generic Name | STRIPPER, VEIN, DISPOSABLE |
Baseline Model No | NA |
Baseline Catalog No | 63-4031 |
Baseline ID | NA |
Baseline Device Family | CODMAN DISPOSABLE VEIN STRIPPER |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 60 |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | Y |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2002-08-13 |