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Flow Beverages Inc. Recall: 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),

United States

TerminatedClass II

Company
Flow Beverages Inc.
Product
Flow Alkaline Spring Water - Organic lemon & ginger flavored…
Recall date
February 17, 2022
Terminated
March 8, 2024
Source
FDA

Reason for recall

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),

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
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

Distribution

  • The product was distributed to the following States: MA
  • PA
  • AI
  • NJ
  • ME
  • NH
  • VT
  • MD
  • VA
  • IL
  • MO
  • DE

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0897-2022
Event ID
89628
Status
Terminated
Classification
Class II
Company
Flow Beverages Inc.
Product description
Flow Alkaline Spring Water - Organic lemon & ginger flavored water. 500 ml unit . Tetra Pak paper carton.
Quantity
854 cases of 12 units (total)
Reason
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),
Recall initiation date
February 17, 2022
Report date
March 30, 2022
Classification date
Not published in this source record
Termination date
March 8, 2024
Distribution pattern
The product was distributed to the following States: MA, PA, AI, NJ,ME, NH, VT,MD, VA,IL,MO,DE
UPC, lot, and code information
Lot 2023AUG29 V5 2023AUG29 V5 UPC 628055429449 628055429425
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Other products recalled under this same event

This recall shares FDA event ID 89628 with 1 other product entry in Public Health Trace.

FDA Recall United States Terminated Historical recordClass II

Flow Beverages Inc.

Product
Flow Alkaline Spring Water - Organic lemon & ginger flavored…
Published
March 30, 2022
Distribution
The product was distributed to the follo…

View recall →

Responsible company: Flow Beverages Inc.

Other recalls from Flow Beverages Inc.

FDA Recall United States Terminated Historical recordClass II

Flow Beverages Inc.

Product
Flow Alkaline Spring Water - Organic lemon & ginger flavored…
Published
March 30, 2022
Distribution
The product was distributed to the follo…

View recall →

Distribution map

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.

Distribution map
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.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

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.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

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.