United States
TerminatedClass II
Flow Beverages Inc., 33 Lakeview CT., Verona, VA, 24482 is initiating a recall of Flow Alkaline Spring Water - Organic lemon & ginger flavored water, 500 ml 12 units per case, Lots 2023AUG29 V5 and 2023AUG29 V5 because of four (4) customer complaints of alleged adverse reactions following the consumption of Flow organic lemon + ginger flavored water, 16.9 fl oz. (500 ml),
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Flow Alkaline Spring Water - Organic lemon & ginger flavored water. 500 ml unit . Tetra Pak paper carton. | Not published in this source record | 854 cases of 12 units (total) | Lot 2023AUG29 V5 2023AUG29 V5 UPC 628055429449 628055429425 |
This recall shares FDA event ID 89628 with 1 other product entry in Public Health Trace.
FDA Recall United States TerminatedTerminated: March 8, 2024Historical recordClass II
Responsible company: Flow Beverages Inc.
FDA Recall United States TerminatedTerminated: March 8, 2024Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Massachusetts | 1 |
| Pennsylvania | 1 |
| New Jersey | 1 |
| Maine | 1 |
| New Hampshire | 1 |
| Vermont | 1 |
| Maryland | 1 |
| Virginia | 1 |
| Illinois | 1 |
| Missouri | 1 |
| Delaware | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
This record is preserved as published by FDA, as of March 8, 2024.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
Reconnecting to the server…
We lost the connection to the server.
Your session has expired.
