NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed Turbo-Elite Laser Atherectomy Catheter is indicated for use in the treatment, including atherectomy, of infrainguinal stenoses and occlusions. This model is not cleared for marketing in the US.
FDA Recall Z-0024-2026 · Posted 2025-10-02
Recalling FirmNortheast Scientific Inc.
Recall StatusOpen, Classified
Product CodeQTF
Date Initiated2025-08-29
Product Quantity616 units
Reason for Recall
Potential for breaches in the sterile barrier packaging, compromising sterility assurance.
Firm Action
Northeast Scientific notified consignees via an "URGENT: Medical Device Recall Notification" letter dated 8/29/2025 and email. Consignees were instructed to immediately discontinue use of affected products, quarantine and return any unused affected units, and complete and return the enclosed Recall Response Form, even if you no longer have any affected product. If product were further distributed, consignees were instructed to notify those customers immediately and ensure they also discontinue use and return the devices.
Northeast Scientific will provide replacement product (if available) or credit for returned product. In addition, Northeast Scientific has initiated an investigation and is implementing corrective actions to prevent recurrence.
If you have any questions or concerns, please reach out to your Northeast Scientific Sales Representative or contact us at [email protected] or 203-756-2111.
Root Cause
Process control
Distribution Pattern
US Nationwide distribution to CA, FL, IL, KS, LA, MD, MI, MO, NC, NJ, NM, NV, NY, PA, TN, TX, VA.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.