Flosonics Medical (R/A 1929803 ONTARIO CORP.): Device Recall
Recall #Z-2517-2025 · 08/07/2025
Class III: Low Risk
Recall Details
- Recall Number
- Z-2517-2025
- Classification
- Class III
- Product Type
- Device
- Recalling Firm
- Flosonics Medical (R/A 1929803 ONTARIO CORP.)
- Status
- Ongoing
- Date Initiated
- 08/07/2025
- Location
- Toronto, N/A, Canada
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 9
Reason for Recall
Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it should read 2026-06-20.
Product Description
FloPatch FP120, REF: FP120-FOT01-005
Distribution Pattern
US Nationwide distribution in the state of California.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.