Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Video Bronchoscope Recalled by Pentax of America Inc Due to This field action serves to retrospectively document the...

Date: January 11, 2011
Company: Pentax of America Inc
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Pentax of America Inc directly.

Affected Products

Video Bronchoscope

Quantity: 1,349 - (Total - US) and 352 (Total - OUS)

Why Was This Recalled?

This field action serves to retrospectively document the actions that were taken by Pentax to correct the loose suction arms on eleven (11) models of endoscopes and to notify FDA of these actions taken in 2010-2011.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Pentax of America Inc

Pentax of America Inc has 28 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report