Z-1860-2016Class II

Endoscope; ED-530XT Operation Manual 'Operation and Preparation' and 'Cleaning, Disinfection and Storage'

Name: Z-1860-2016 Endoscope; ED-530XT Operation Manual 'Operation and Preparation' and 'Cleaning, Disinfection and Storage'
Creator: Fujifilm Medical Systems U.S.A., Inc.
Published: 2015-12-23
License: https://open.fda.gov/license/

FUJIFILM Healthcare Americas Corporation / initiated 2015-12-23 / Terminated

FDA source

Fujifilm Medical Systems U.S.A., Inc. began a recall of Endoscope; ED-530XT Operation Manual 'Operation and Preparation' and 'Cleaning, Disinfection and Storage' on 2015-12-23. FDA classified it as Class II and gives the reason as "This correction is in response to publicized reports of multi-drug resistant bacteria on endoscopes used for Endoscopic Retrograde Cholangiopancreatogram (ERCP) procedures". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-1860-2016
Classification: Class II
Status: Terminated
Initiated: 2015-12-23
Posted: 2016-05-31
Terminated: 2018-01-18
Recalling firm: FUJIFILM Healthcare Americas Corporation
Product: Endoscope; ED-530XT Operation Manual 'Operation and Preparation' and 'Cleaning, Disinfection and Storage'
Product code: FDT Duodenoscope And Accessories, Flexible/Rigid
Reason for recall: This correction is in response to publicized reports of multi-drug resistant bacteria on endoscopes used for Endoscopic Retrograde Cholangiopancreatogram (ERCP) procedures.
FDA root cause: Other
Action: Fujifilm issued a urgent field correction/Tracking/Verification form on 12/23/2015.
Quantity in commerce: 1473 units
Distribution: Nationwide Distribution.
Product codes and lots: All distribution dates :3/2003-4/2016

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1860-2016
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1860-2016	Class II	Terminated	Voluntary: Firm initiated	2016-06-08	2016-05-31
Z-1861-2016	Class II	Terminated	Voluntary: Firm initiated	2016-06-08	2016-05-31
Z-1862-2016	Class II	Terminated	Voluntary: Firm initiated	2016-06-08	2016-05-31
Z-1863-2016	Class II	Terminated	Voluntary: Firm initiated	2016-06-08	2016-05-31
Z-1864-2016	Class II	Terminated	Voluntary: Firm initiated	2016-06-08	2016-05-31

Product code FDT

K042076Class IIFujinon G5 Duodenscopes; G5 Duodenoscopes, Ed-450Xt5, Ed-250Xt5Fujinon, Inc. / cleared 2004-11-18

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 2026-10-14, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)