Z-1007-2019Class II

Olympus GF-UCT180 Ultrasound Gastrovideoscope -

Name: Z-1007-2019 Olympus GF-UCT180 Ultrasound Gastrovideoscope -
Creator: Olympus Corporation of the Americas
Published: 2018-12-17
License: https://open.fda.gov/license/

OLYMPUS Corporation of the Americas / initiated 2018-12-17 / Terminated

FDA source

Olympus Corporation of the Americas began a recall of Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the... on 2018-12-17. FDA classified it as Class II and gives the reason as "The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1007-2019
Classification: Class II
Status: Terminated
Initiated: 2018-12-17
Posted: 2019-03-12
Terminated: 2020-11-18
Recalling firm: OLYMPUS Corporation of the Americas
Product: Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
Product code: IYN System, Imaging, Pulsed Doppler, Ultrasonic
Reason for recall: The adhesive used in the repair of the endoscope was incorrectly prepared. It is unknown what affect the nonconforming adhesive mixture would have on the durability or effectiveness of the gluing operation for the endoscope repair.
FDA root cause: Under Investigation by firm
Action: Customers were contacted via telephone on 12/17/18. Customers were also sent notification letters on 1/2/19.
Quantity in commerce: 1
Distribution: US Nationwide distribution in the states of CT, IL, MN, MO, and NC.
Product codes and lots: Serial Number 7621683

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1007-2019
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1007-2019	Class II	Terminated	Voluntary: Firm initiated	2019-03-20	2019-03-12
Z-1008-2019	Class II	Terminated	Voluntary: Firm initiated	2019-03-20	2019-03-12
Z-1009-2019	Class II	Terminated	Voluntary: Firm initiated	2019-03-20	2019-03-12
Z-1010-2019	Class II	Terminated	Voluntary: Firm initiated	2019-03-20	2019-03-12

Product code IYN

K093395Class IIOlympus Gf Type Uc180, Olympus Gf Type Uct180 Evis Exera II Ulatrasound GastrovideoscopeOlympus Medical Systems Corporation / cleared 2010-06-17

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)