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Recall Observatory FDA recall evidence

Device product

Duodenoscope and accessories, flexible/rigid - Product Usage: used with an Olympus video system center, light source, documentation equipment, monitor, Endo Therapy accessories (such as biopsy forceps), and other ancillary equipment for endoscopy and endoscopic surgery within the duodenum.

Z-1292-2021

January 28, 2021

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 87296
Status
Terminated
Classification
Class II
Quantity
1564 devices total (Domestic: 627 devices, Foreign: 937 devices)
Official record key
device-enforcement:Z-1292-2021

Official wording

Reason: Olympus Medical Systems Corporation (OMSC) has received complaints of mucosal injury associated with the forceps elevator region of the TJF-Q190V duodenoscope, including the distal cover (model MAJ- 2315).

Code information: Model: TJF-Q190V

Distribution pattern: Worldwide distribution - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NH, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY and the countries of Japan, Europe, Australia.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Olympus Medical Systems Corporation (OMSC) has received complaints of mucosal injury associated with the forceps elevator region of the TJF-Q190V duodenoscope, including the distal cover (model MAJ- 2315).