Flosonics recalls FloPatch FP120 devices with a shipping label showing 2025-06-20 instead of 2026-06-: Check packaging for expiry date mismatch.
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.
Flosonics is recalling FloPatch FP120 medical devices because the shipping packaging shows an incorrect expiry date (2025-06-20 instead of 2026-06-20). This could lead to confusion about when the device expires, potentially affecting medical use.
The shipping packaging has a human-readable expiry date that incorrectly shows June 20, 2025 instead of June 20, 2026. This mismatch could cause users to think the device expires earlier than it actually does, potentially leading to improper use or safety concerns.
Users of FloPatch FP120 devices who purchased them with a shipping label showing 2025-06-20 instead of 2026-06-20. Patients using these devices for medical purposes are most at risk if they rely on the expiry date for device safety.
Check the shipping packaging for a date label that says 2025-06-20 instead of 2026-06-20. The product lot number is 03250602 and the UDI-DI is 10627987360148.
Look for a shipping label that shows 2025-06-20 instead of 2026-06-20.
The shipping packaging has an incorrect expiry date (2025-06-20 instead of 2026-06-20), which could lead to confusion about when the device expires.
Check the shipping packaging for a date label that says 2025-06-20 instead of 2026-06-20. The product lot number is 03250602 and the UDI-DI is 10627987360148.
The recall record does not specify a remedy, so no action is required beyond checking the expiry date on the packaging.
We’ve drafted a message you can send Flosonics to request your refund or repair — edit it as you like.
Subject: Recall Z-2517-2025 — Flosonics Flosonics Hello, I own a Flosonics that is covered by recall Z-2517-2025 from Flosonics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
