Reported Sep 10, 2025 · Ongoing

FloPatch FP120, REF: FP120-FOT01-005

Flosonics Medical (R/A 1929803 ONTARIO CORP.)

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Flosonics Medical (R/A 1929803 ONTARIO CORP.) · Fourth Floor, Oneeleven · Toronto, N/A · N/A

Is this the product you have?

  • FloPatch FP120
  • REFFP120-FOT01-005
Lot codes and dates
  • UDI-DI10627987360148
  • Lot03250602
Amount recalled
9

Where it was sold

  • Nationwide
  • CA

Why it was recalled

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.

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:21 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.