Reported Sep 22, 2025 · Announced

Olympus Corporation recalls Olympus ViziShot 2 FLEX (19G) EBUS -TBNA needles due to Device Components May Detach During Procedures

Olympus Corporation

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

What you should do

Stop using the product and follow the return or refund instructions in the firm's announcement.

Is this the product you have?

  • ViziShot 2
  • FLEX (19G) EBUS -TBNA needles BrandOlympus. Medical Devices

Why it was recalled

Device Components May Detach During Procedures

The agency has not ranked the risk yet — treat the notice as a caution.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Olympus Corporation recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration

Read the FDA (recalls & safety alerts) notice

Data as of Sep 19, 5:56 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.