Home › NORTH EAST SCIENTIFIC INC › NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter
NES Reprocessed 0.9mm RX Turbo Elite Laser Atherectomy Catheter
NORTH EAST SCIENTIFIC INC · Model R-410-154 · UDI-DI 00850044399062
QTF
Prescription
1
510(k) clearances
0
Adverse events
8
Recalls
1
Facilities
Description
The device is the Phillips 0.9mm RX Turbo Elite Laser Atherectomy catheter that is reprocessed by Northeast Scientific, Inc. (NES)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
| 2025-08-29 | Northeast Scientific Inc. | Potential for breaches in the sterile barrier packaging, compromising sterility assurance. |
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.