Olympus Corporation of the Americas recalls

Olympus Corporation of the Americas has 415 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 2 Sep 2026. 324 are still ongoing. 140 were reported in the last 12 months.

Total recalls415since 2015
Last 12 months140reported
Class I4411% of total
Ongoing324latest 2 Sep 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 44 11%Class II 369 89%Class III 2 0%

Why olympus corporation of the americas is recalled

By year

Ongoing olympus corporation of the americas recalls

324 active

All olympus corporation of the americas recalls, newest first

415 total
ReportedClassRecallCompanyReasonWhere
DeviceCLASS IIPowerseal (in diameter) (long), Curved Jaw Sealer & Divider recalledOlympus Corporation of the AmericasLabeling ErrorsNationwide
DeviceCLASS IIOlympus 4K UHD LCD Monitor recalled by Olympus Corporation of theOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOlympus High Flow Insufflation Unit - UHI recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOlympus Toomey Evacuator 50cc with Adaptor recalledOlympus Corporation of the AmericasSterilityNationwide
DeviceCLASS IIOlympus Glass Body for 194 Ellik Evacuator recalledOlympus Corporation of the AmericasSterilityNationwide
DeviceCLASS IIOlympus Toomey Evacuator 30cc with Adaptor recalledOlympus Corporation of the AmericasSterilityNationwide
DeviceCLASS IIOlympus Ellik Evacuator Includes Glass Body recalledOlympus Corporation of the AmericasSterilityNationwide
DeviceCLASS IIOlympus Single Use Distal Cover recalled by Olympus Corporation of theOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOlympus Thunderbeat II Shears w/Ultrasonic Mode recalledOlympus Corporation of the AmericasOtherPA
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOlympus Thunderbeat II Shears w/Ultrasonic Mode recalledOlympus Corporation of the AmericasOtherPA
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOlympus Thunderbeat II Shears w/Ultrasonic Mode recalledOlympus Corporation of the AmericasOtherPA
DeviceCLASS IIOer-elite Endoscope Reprocessor Connecting Tubes recalledOlympus Corporation of the AmericasOtherNationwide
DeviceCLASS IIOlympus Thunderbeat II Shears w/Ultrasonic Mode recalledOlympus Corporation of the AmericasOtherPA
DeviceCLASS IISoltive Pro Laser System Tfl-sls recalled by Olympus Corporation of theOlympus Corporation of the AmericasDevice MalfunctionNationwide
DeviceCLASS IISoltive Premium Laser System Tfl-pls recalledOlympus Corporation of the AmericasDevice MalfunctionNationwide
DeviceCLASS IIHALO PKS Cutting Forceps recalled by Olympus Corporation of theOlympus Corporation of the AmericasDevice MalfunctionNationwide
DeviceCLASS IIOlympus PKS Cutting Forceps PKS Cutting Forceps recalledOlympus Corporation of the AmericasDevice MalfunctionNationwide
DeviceCLASS IIEverest Bipolar Cutting Forceps recalled by Olympus Corporation of theOlympus Corporation of the AmericasDevice MalfunctionNationwide
DeviceCLASS IIEverest Bipolar Cutting Forceps recalled by Olympus Corporation of theOlympus Corporation of the AmericasDevice MalfunctionNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.