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CUSA® NXT
INTEGRA LIFESCIENCES (IRELAND) LIMITED · Model 1532024 · UDI-DI 10381780040255
LFL
Prescription
1
510(k) clearances
68,850
Adverse events (81 deaths)
109
Recalls
141
Facilities
Description
MRI Tubing Kit Extension:The Selector tubing connects the handpiece to the IV fluid and connects the handpiece to the suction canister on the CUSA® Selector / CUSA NXT console.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-06 | Integra LifeSciences Corp. (NeuroSciences) | Software issue that renders the touch screen unresponsive. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
| 2025-10-22 | Olympus Corporation of the Americas | Firm is initiating a removal due to continued reports of adverse events. |
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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.