The OLYMPUS MEDICAL SYSTEMS CORP. OER-PRO and OER-ELITE endoscope reprocessors (model/catalogue numbers OER-PRO and OER-ELITE; affected units identified by lot/serial numbers consisting of more than 10 numbers — contact the manufacturer for specifics) are affected. Olympus received notification of a fire-related incident involving the OER-PRO and is reminding users to follow the warnings, cautions and inspections in all Olympus endoscope reprocessor operation manuals. Contact the manufacturer for additional information.
What's being recalled
Companies: Olympus Medical Systems Corp., 2951 Ishikawa-Cho, Hachioji-Shi, Tokyo-To, Japan, 192-8507.
How to identify it
Affected products: OER-PRO Endoscope Reprocessor; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: OER-PRO
Affected products: Endoscope Reprocessor; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: OER-ELITE
The hazard
Olympus received notification of a fire-related incident involving the OER-PRO. Olympus is providing warnings/cautions reminders associated with all Olympus endoscope reprocessors and reminding users to follow the warnings/cautions and inspections outlined in all Olympus endoscope reprocessor operation manuals.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)