Oer-pro And Oer-elite Endoscope Reprocessor
Recall Summary OER-PRO and OER-Elite Endoscope Reprocessor devices are being recalled because they are not performing as intended. This recall affects devices distributed across Canada. The FDA has classified this as a Class I recall, which is the most serious classification level.
- Product
- OER-PRO and OER-Elite Endoscope Reprocessor
- Reason
- Performance
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-01-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/f70954cb-8604-4725-a508-fa0ccecd1ba6