Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported January 8, 2014
Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding brand, Item # 1881-060.
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
The recall
Kirkman Group Inc. issued this moderate-severity FDA Food recall — Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol.
- Moderate
- severity level
- Class II
- classification
- January 8, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1353-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1353-2014) was formally reported on January 8, 2014, with the manufacturer initiating the action on November 15, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Kirkman Group Inc. is listed as the recalling firm, operating out of Lake Oswego, OR. Federal records list the affected scope as 6099 bottles (5489 bottles in US and 610 outside the US).
The documented reason for this recall is: Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol Distribution data in the federal record shows the product reached: distributed worldwide. 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, 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 — 711 dietary supplements recalls on record
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.
Affected scope
6099 bottles (5489 bottles in US and 610 outside the US)
Related Recalls
6
5 from same agency
Product description
Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding brand, Item # 1881-060.
Reason for recall
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1353-2014 |
| Date reported | January 8, 2014 |
| Date initiated | November 15, 2013 |
| Recalling firm | Kirkman Group Inc. |
| Firm location | Lake Oswego, OR |
| Affected scope | 6099 bottles (5489 bottles in US and 610 outside the US) |
| Distribution | distributed worldwide |
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-1353-2014) 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? ▼
Biofilm Defense, Kirkman brand, Item # 0881-060 and 5881-060 Biofilm Defense, Pure Compounding brand, Item # 1881-060.. Recalled by Kirkman Group Inc.. Units affected: 6099 bottles (5489 bottles in US and 610 outside the US).
Why was this product recalled? ▼
Firm is recalling dietary supplements containing a raw material which may contain >0.3 ppb chloramphenicol
Which agency issued this recall? ▼
This recall was issued by the FDA Food on January 8, 2014. Severity: Moderate. Recall number: F-1353-2014.
Where was the recalled product distributed? ▼
Distribution: distributed worldwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1353-2014) 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.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported January 8, 2014.
- 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.