Sustainable Technologies
Provision · Model ST279-350-201 · UDI-DI 00810041638366
NUJ
Prescription
1
510(k) clearances
772
Adverse events (2 deaths)
20
Recalls
23
Facilities
Description
Serfas Energy Lateral RF Ablation Probe
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 |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.