MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-06 for VISISTAT 35W 6/BOX 528235 manufactured by Teleflex Medical.
[182433499]
(b)(4). The device has not been returned for investigation. Teleflex will continue to monitor and trend related events.
Patient Sequence No: 1, Text Type: N, H10
[182433500]
It was reported that the staples will not close properly.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3003898360-2020-00275 |
MDR Report Key | 9800566 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2020-03-06 |
Date of Report | 2020-02-17 |
Date of Event | 2020-02-13 |
Date Mfgr Received | 2020-02-17 |
Date Added to Maude | 2020-03-06 |
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 | EFFIE JEFFERSON |
Manufacturer Street | 3015 CARRINGTON MILL BLVD |
Manufacturer City | MORRISVILLE 27560 |
Manufacturer Country | US |
Manufacturer Postal | 27560 |
Manufacturer Phone | 9194332672 |
Manufacturer G1 | TELEFLEX MEDICAL |
Manufacturer Street | RANCHO EL DESCANSO |
Manufacturer City | TECATE 21478 |
Manufacturer Country | MX |
Manufacturer Postal Code | 21478 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VISISTAT 35W 6/BOX |
Generic Name | STAPLE, REMOVABLE (SKIN) |
Product Code | GDT |
Date Received | 2020-03-06 |
Catalog Number | 528235 |
Lot Number | 73C190074 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | TELEFLEX MEDICAL |
Manufacturer Address | MORRISVILLE NC |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-06 |