PlainRecalls
ModerateClass IITerminated

FDA Food recall · Reported November 2, 2016

Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Recall #
F-0255-2017
Affected scope
8,232 bottles
Initiated
August 8, 2016
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Pharmatech LLC recalled Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary su… - a moderate-severity action.

Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary su… was recalled by Pharmatech LLC in November 2, 2016. Reason: Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia …. Check the official notice for the remedy. Verify recall #F-0255-2017 with the FDA Food before acting.

The recall

Pharmatech LLC issued this moderate-severity FDA Food recall-Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia ….

Moderate
severity level
Class II
classification
November 2, 2016
reported

Sourced from official FDA Food enforcement records. Verify recall #F-0255-2017 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This recall's affected scope, documented in the Recall Profile below, stays within a single-region or limited-distribution footprint. Distribution scope (see Distribution below) 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, 5 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.

Dietary Supplements recalls over time

Where this recall sits in its category - 2,014 dietary supplements recalls on record

0100200300400 20072010201320162019202220252026 21
Severity1906864652High severity (most serious)Moderate severityLow severity
Where this agency-classified recall sits among FDA Class I/II/III notices

Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. 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.

Product description

Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

Reason for recall

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

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-0255-2017
Date reported November 2, 2016
Date initiated August 8, 2016
Recalling firm Pharmatech LLC
Firm location Davie, FL
Affected scope 8,232 bottles
Distribution FL, MI, MS, and OH.

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-0255-2017) 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?
Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.. Recalled by Pharmatech LLC. Units affected: 8,232 bottles.
Why was this product recalled?
Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.
Which agency issued this recall?
This recall was issued by the FDA Food on November 2, 2016. Severity: Moderate. Recall number: F-0255-2017.
Where was the recalled product distributed?
Distribution: FL, MI, MS, and OH..
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.

Nationwide recalls with similar severity or category timing

Food and dietary-supplement notices outside this firm and state, matched by severity timing and product category.

Compare this recall with Goody King Magnetic Building Cubes and Blocks Recalled Due … → · All Dietary Supplements recalls

This recall: FDA Food, reported November 2, 2016. Severity classes follow each agency's own taxonomy; related-recall context is computed across the full archive.

Methodology · Corrections · Archive as of August 2026