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U.S. Department of Health and Human Services

Class 2 Device Recall EVIS EXERA Duodenovideoscope OLYMPUS TJF Type 190V

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 Class 2 Device Recall EVIS EXERA Duodenovideoscope OLYMPUS TJF Type 190Vsee related information
Date Initiated by FirmJanuary 28, 2021
Create DateMarch 22, 2021
Recall Status1 Terminated 3 on March 13, 2024
Recall NumberZ-1292-2021
Recall Event ID 87296
510(K)NumberK193182 
Product Classification Duodenoscope and accessories, flexible/rigid - Product Code FDT
ProductDuodenoscope 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.
Code Information Model: TJF-Q190V
Recalling Firm/
Manufacturer		 Olympus Corporation of the Americas
3500 Corporate Pkwy
PO Box 610
Center Valley PA 18034-0610
For Additional Information ContactLaura Storms
484-896-5688
Manufacturer Reason
for Recall		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).
FDA Determined
Cause 2		Under Investigation by firm
ActionOn 2/5/2021, Olympus issued Urgent Device Correction notices to customers via letter informing them Olympus has identified an increase in the number of complaints from customers reporting that mucosal tissue was found within the single-use distal cover, MAJ-2315, after withdrawing the TJF-Q190V duodenoscope from the patient. In the reported complaints, the user facilities have reported mucosal injuries in the esophagus, stomach, and duodenum. Olympus is thoroughly investigating the root cause or causes of these reported events. This notice included information that may reduce the potential occurrence of similar incidents.
Quantity in Commerce1564 devices total (Domestic: 627 devices, Foreign: 937 devices)
DistributionWorldwide 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.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = FDT
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