FDA Device Intelligence
Home › OLYMPUS MEDICAL SYSTEMS CORP. › THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type X

THUNDERBEAT 5 mm, 45 cm, Front-actuated Grip Type X

OLYMPUS MEDICAL SYSTEMS CORP. · Model TB-0545FCX · UDI-DI 04953170392160

LFLGEI Prescription
10
510(k) clearances
68,850
Adverse events (81 deaths)
109
Recalls
141
Facilities

Description

THUNDERBEAT 5mm, 45cm, Front-actuated Grip Type X

Recalls

DateFirmReason
2026-03-06Integra LifeSciences Corp. (NeuroSciences)Software issue that renders the touch screen unresponsive.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.
2025-10-22Olympus Corporation of the AmericasFirm is initiating a removal due to continued reports of adverse events.

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 docs
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.