Northeast Scientific Inc. recalls
Every recall we track for Northeast Scientific Inc. — 9 in all, from 2021–2025 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Northeast Scientific Inc. peaked in 2025 (8); 9 since 2017.
All FDA recall records for Northeast Scientific Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 1 | 0 | 1 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 8 | 0 | 8 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Northeast Scientific Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Northeast Scientific Inc. recalls
2 shown- Lower riskMedical device
Northeast Scientific Inc. recalls NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed
Northeast Scientific recalls NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter (Model R-417-156) due to potential sterile packaging breaches. Affected units sold with expiration dates before August 29, 2026.
Northeast ScientificAug 29, 2025 - Lower riskMedical device
Northeast Scientific Inc. recalls NES Reprocessed Visions PV .035 IVUS Catheter, Sterile. For use in the evaluation of vascular morphology in blood
Northeast Scientific recalls specific lots of reprocessed IVUS catheters due to unsafe reprocessing cycles. This device is used for blood vessel imaging and may cause harm if reprocessed beyond the approved limit.
Northeast ScientificApr 26, 2021
Northeast Scientific Inc. recall questions
How many recalls has Northeast Scientific Inc. had?
9 recalls from Northeast Scientific Inc. are on record with U.S. safety agencies, from 2021–2025.
What is the most recent Northeast Scientific Inc. recall?
Northeast Scientific Inc. recalls NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter. Model Number: R-417-156. The NES Reprocessed, dated Aug 29, 2025. Every Northeast Scientific Inc. recall is listed on this page, newest first.
What should I do if I have a recalled Northeast Scientific Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Northeast Scientific Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.