Reported Jan 29, 2025 · Ongoing

Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm,…

Olympus Corporation of the Americas

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Olympus Corporation of the Americas · 3500 Corporate Pkwy · Center Valley, PA · 18034-8229

Is this the product you have?

  • Brand NameOlympus Thunderbeat Front-Actuated Grip
  • Type S Hand Instrument Product Name
    • THUNDERBEAT 5 mm
    • 20 cm
  • Front-actuated Grip Type S Model NumberTB-0520FCS
  • Catalog Number/Product CodeN5424110¿
  • Software VersionN/A
  • Product DescriptionThunderbeat instrument is a sterile, single use item which is intended to be used with the Ultrasonic Generator (USG-400), the Electrosurgical Generator (WSG-400), and the Thunderbeat Transducer, (TD-TB400)
Lot codes and dates
  • ModelTB-0520FCS
  • Catalog Number/Product CodeN5424110¿
  • UDI
    • 04953170383595
    • 04953170383592
  • LotsAll
Amount recalled
11,329 units (OUS ONLY)

This recall covers 11 products

The agency filed one notice per product. You are reading one of them; the other 10 are below.

Where it was sold

  • Nationwide
  • GA

Why it was recalled

The probe tips of the hand instruments are being damaged or breaking including pad damage and detachment.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.