FloPatch FP120, REF: FP120-FOT01-005
Class I - Dangerous 🏥 Medical Devices
Recalled: August 7, 2025 Flosonics Medical (R/A 1929803 ONTARIO CORP.) Other Medical Devices
Nationwide
What Should You Do?
- Check if you have this product: UDI-DI: 10627987360148. Lot: 03250602
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Flosonics Medical (R/A 1929803 ONTARIO CORP.)
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
FloPatch FP120, REF: FP120-FOT01-005
Product Codes/Lot Numbers:
UDI-DI: 10627987360148. Lot: 03250602
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2517-2025