FloPatch FP120, REF: FP120-FOT01-005
Reported: September 10, 2025 Initiated: August 7, 2025 #Z-2517-2025
Product Description
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.
Details
- Recalling Firm
- Flosonics Medical (R/A 1929803 ONTARIO CORP.)
- Units Affected
- 9
- Distribution
- US Nationwide distribution in the state of California.
- Location
- Toronto, N/A
Frequently Asked Questions
What product was recalled? ▼
FloPatch FP120, REF: FP120-FOT01-005. Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.). Units affected: 9.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 10, 2025. Severity: Low. Recall number: Z-2517-2025.
Related Recalls
FDA Devices Moderate
Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA Convenience Kit - FXX VS0644.25-FXX 3.2…
Vortex Surgical Inc. · 2026-02-11
FDA Devices Moderate
COULTER DxH Diluent, REF 628017 COULTER DxH ECO Diluent REF C67250 For use as an isotonic buffered diluent in conju…
Beckman Coulter, Inc. · 2026-02-11
FDA Devices Moderate
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These inst…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 Product Description: These in…
Olympus Corporation of the Americas · 2026-02-11
FDA Devices Moderate
Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558 Software Version: Not Applicable Produc…
Fujirebio Diagnostics, Inc. · 2026-02-11