Facility

FLOSONICS MEDICAL (R/A 1929803 ONTARIO CORP.)

1 recall(s) on record — most severe on record: Class III.

Key facts

1recalls · worst Class III

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3015139886
Establishment type	Manufacture Medical Device; Export Device to the United States But Perform No Other Operation on Device; Reprocess Single-Use Device
Location	325 Front St W Toronto Ontario, CA M5V 2Y1
Registration status	Active · expires 2026
Parent company	Flosonics Medical (R/A 1929803 Ontario Corp.) (owner-operator 10065763)
Brand names	FloPatch

Activity by year

Recalls (1)

Devices registered here (1)

Flowmeter, Blood, Cardiovascular
Product code DPW (opens in a new tab) · Class II · Cardiovascular · 21 CFR 870.2100

Recalls & enforcement

Class IIIOngoing2025-08-07
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.

All facilities operated by Flosonics Medical (R/A 1929803 Ontario Corp.)

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “FLOSONICS MEDICAL (R/A 1929803 ONTARIO CORP.) (FEI 3015139886) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3015139886-flosonics-medical-r-a-1929803-ontario-co/

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