MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2002-11-05 for SPT-05172 IN CARDIAC CATH PACK DYNJV0193B * manufactured by Medline Industries, Inc..
[256445]
Reportedly the tips of the hemostat were sharp and an artery on a patient was allegedly punctured. Pressure was applied to the site and no further medical treatment was required.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1423395-2002-00005 |
MDR Report Key | 426790 |
Report Source | 05,07 |
Date Received | 2002-11-05 |
Date of Report | 2002-11-05 |
Date of Event | 2002-10-07 |
Date Mfgr Received | 2002-10-07 |
Device Manufacturer Date | 2002-06-01 |
Date Added to Maude | 2002-11-13 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | ANDREA HAFERKAMP |
Manufacturer Street | ONE MEDLINE PLACE |
Manufacturer City | MUNDELEIN IL 60060 |
Manufacturer Country | US |
Manufacturer Postal | 60060 |
Manufacturer Phone | 8478372759 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SPT-05172 IN CARDIAC CATH PACK |
Generic Name | HEMOSTAT FORCEPS IN CARDIAC CATH PACK |
Product Code | HRQ |
Date Received | 2002-11-05 |
Returned To Mfg | 2002-10-08 |
Model Number | DYNJV0193B |
Catalog Number | * |
Lot Number | 02FD1953 |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 415815 |
Manufacturer | MEDLINE INDUSTRIES, INC. |
Manufacturer Address | ONE MEDLINE PLACE MUNDELEIN IL 60060 US |
Baseline Brand Name | HEMOSTAT FORCEPS IN CARDIAC CATH PACK |
Baseline Model No | DYNJV0193B |
Baseline Device Family | PROV |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2002-11-05 |