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NES Reprocessed RF Stylet (RFS)

NORTH EAST SCIENTIFIC INC · Model R-RFS2-6-12 · UDI-DI 00850044399031

NUJ Prescription
1
510(k) clearances
773
Adverse events (2 deaths)
20
Recalls
22
Facilities

Recalls

DateFirmReason
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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
2025-10-01Medline Industries, LPMedline 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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Data 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.