PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported April 5, 2017

KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce

Elevated patulin levels.

Recall #
F-1805-2017
Affected scope
80 BIB and 88 cases of 2 oz immunity shots (total for all products)
Initiated
February 24, 2017
Verify with FDA Food →
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Freshbev LLC recalled KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce — a moderate-severity action.

KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce was recalled by Freshbev LLC in April 5, 2017. Reason: Elevated patulin levels.. Check the official notice for the remedy. Verify recall #F-1805-2017 with the FDA Food before acting.

The recall

Freshbev LLC issued this moderate-severity FDA Food recall — Elevated patulin levels..

Moderate
severity level
Class II
classification
April 5, 2017
reported

Sourced from official FDA Food enforcement records. Verify recall #F-1805-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-1805-2017) was formally reported on April 5, 2017, with the manufacturer initiating the action on February 24, 2017. It is classified under Moderate severity (Class II), with a current status of Terminated. Freshbev LLC is listed as the recalling firm, operating out of New Haven, CT. Federal records list the affected scope as 80 BIB and 88 cases of 2 oz immunity shots (total for all products).

The documented reason for this recall is: Elevated patulin levels. Distribution data in the federal record shows the product reached: CT, FL, CO, NY, NV. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Food recalls over time

Where this recall sits in its category — 25,414 food recalls on record

-1,00001,0002,0003,000 20052008201120142017202020232026 436

Where this recall sits in the database

Severity2366872097High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 100,165 recalls in the database, 23,668 are high severity, 72,097 moderate, and 4,400 low. This recall is classified moderate severity.

Counts reflect market size and reporting activity, not inherent danger — we do not rank products by risk from raw recall volume.

Severity

Moderate

Affected scope

80 BIB and 88 cases of 2 oz immunity shots (total for all products)

Related Recalls

6

6 from same agency

Product description

KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce

Reason for recall

Elevated patulin levels.

Recall Profile

Structured summary of the FDA Food recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Moderate (Class II)
Status Terminated
Recall number F-1805-2017
Date reported April 5, 2017
Date initiated February 24, 2017
Recalling firm Freshbev LLC
Firm location New Haven, CT
Affected scope 80 BIB and 88 cases of 2 oz immunity shots (total for all products)
Distribution CT, FL, CO, NY, NV

Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (F-1805-2017) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Food before acting — recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
KEEP REFIGERATED, DEEP BEET Blend 5 Gal, Ripe Liquid Produce. Recalled by Freshbev LLC. Units affected: 80 BIB and 88 cases of 2 oz immunity shots (total for all products).
Why was this product recalled?
Elevated patulin levels.
Which agency issued this recall?
This recall was issued by the FDA Food on April 5, 2017. Severity: Moderate. Recall number: F-1805-2017.
Where was the recalled product distributed?
Distribution: CT, FL, CO, NY, NV.
How do I check if my product is affected by a recall?
Check the product description and recall number (F-1805-2017) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product?
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

Nearby Recalls in This Category

Other recalls in the same product category — useful for spotting patterns across the same defect class or manufacturer.

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Data Sources

Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported April 5, 2017.

  • Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
  • Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
  • Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)

Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records — no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of June 2026.