PlainRecalls
FDA Devices Moderate Class II Terminated

OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector

Reported: October 26, 2016 Initiated: June 23, 2016 #Z-0138-2017

Product Description

OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector

Reason for Recall

New warning requiring Users to conduct duodenoscope precleaning and manual cleaning even when using an Automated Endoscope Reprocessor (AER) that has instructions that may indicate a user could forego certain steps in precleaning and manual cleaning of the endoscopes.

Details

Units Affected
2, 686 units
Distribution
Distributed to: AK,AL,AR,AZ,CA,CO,CT,DC,DE,FL,GA,HI,IA,ID,IL,IN,KS,KY,LA,MA,MD,ME,MI,MN,MO,MS,MT,NC,ND,NE,NH,NJ,NM,NV,NY,OH,OK,OR,PA,RI,SC,TN,TX,UT,VA,VT,WA,WI,WV,WY
Location
Center Valley, PA

Frequently Asked Questions

What product was recalled?
OER-Pro Endoscope Reprocessor, Endoscope washer/disinfector. Recalled by Olympus Corporation of the Americas. Units affected: 2, 686 units.
Why was this product recalled?
New warning requiring Users to conduct duodenoscope precleaning and manual cleaning even when using an Automated Endoscope Reprocessor (AER) that has instructions that may indicate a user could forego certain steps in precleaning and manual cleaning of the endoscopes.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 26, 2016. Severity: Moderate. Recall number: Z-0138-2017.