FloPatch FP120 — Class III medical device recall Z-2517-2025
Ongoing recall by Flosonics Medical (R/A 1929803 ONTARIO CORP.), reported 2025-09-10, distributed nationwide. Flowmeter patch as a human readable expiry date on the outer shipping packaging that reads 2025-06-20 when it
| Recall number | Z-2517-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Flosonics Medical (R/A 1929803 ONTARIO CORP.), Toronto, N/A, Canada |
| Recall initiated | 2025-08-07 |
| Classified | 2025-09-04 |
| Reported by FDA | 2025-09-10 |
| Distributed | Nationwide (US) |
| Quantity | 9 |
| UPC / GTIN / UDI-DI | 10627987360148 |
| Lot numbers | 03250602 |
| Model numbers | FP120-FOT01-005 |
Product
FloPatch FP120, REF: FP120-FOT01-005
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2517-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.