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NES Reprocessed Varicose Vein RF Catheter
NORTH EAST SCIENTIFIC INC · Model CF7-3-60 · UDI-DI 00850044399024
NUJ
Prescription
1
510(k) clearances
772
Adverse events (2 deaths)
20
Recalls
23
Facilities
Description
The NES Reprocessed Varicose Vein RF Catheter (Covidien Closurefast CF7-3-60) is intended for endovascular coagulation of blood vessels in patients with superficial vein reflux.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
| 2025-10-01 | Medline Industries, LP | Medline Renewal has determined that certain areas on the device have the potential to trap residual material, which may remain within the device and, in rare cases, become dislodge |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.