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Recall Observatory FDA recall evidence

Device product

Olympus CHF-CB30S Choledoscope Intended Use: The device was designed to be used with an Olympus TV camera system, light source, TV monitor, endo-therapy accessories and other ancillary equipment for endoscopic diagnosis and treatment within the biliary tract (common bile duct, cystic duct, and hepatic duct).

Z-0119-2021

August 31, 2020

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 86367
Status
Terminated
Classification
Class II
Quantity
193 devices distributed in the U.S. 548 devices distributed globally.
Official record key
device-enforcement:Z-0119-2021

Official wording

Reason: The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the device has been associated with breakage of the insertion section and protrusion of metal parts, as well as breakage and displacement of the rubber on the bending section during surgical procedures.

Code information: All lot codes..

Distribution pattern: US Nationwide Distribution in states of: AK, AZ, CA, FL, GA, IL, LA, MA, ME, MI, MN, MS, NC, NM, NJ, NY, OR, SC, TN, WA, and WI; and International to: Japan.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The CHF-CB30S Device did not have a 510(k) clearance. Additionally, the device has been associated with breakage of the insertion section and protrusion of metal parts, as well as breakage and displacement of the rubber on the bending section during surgical procedures.