Pyrola Joint Formula Recall: Undeclared Diclofenac Risk
GC Natural Nutrition recalls Pyrola Advanced Joint Formula capsules due to undeclared diclofenac and chlorpheniramine. Check your bottle UPC.
Stop using this now
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared diclofenac, a prescription non-steroidal anti-inflammatory drug, and chlorpheniramine, an over-the-counter antihistimine, making this an unapproved drug.
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What happened, in plain English
GC Natural Nutrition, Inc. is recalling Pyrola Advanced Joint Formula capsules because they contain undeclared prescription drug diclofenac and antihistamine chlorpheniramine. This makes the product an unapproved drug that poses health risks to consumers who are unaware of these ingredients. The recall covers all lots distributed nationwide. Read more at govinfonow.com/recall/44176-gc-natural-nutrition-inc-recalls-pyrola-advanced-joint-formula-capsules.
Source Summary by GovInfoNow · govinfonow.com/recall/44176-gc-natural-nutrition-inc-recalls-pyrola-advanced-joint-formula-capsules · Updated October 12, 2026 · FDA enforcement record: FDA #D-1330-2015
Cite this page
“Pyrola Joint Formula Recall: Undeclared Diclofenac Risk.” GovInfoNow, updated October 12, 2026. https://govinfonow.com/recall/44176-gc-natural-nutrition-inc-recalls-pyrola-advanced-joint-formula-capsules. Based on FDA recall #D-1330-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1330-2015%22&limit=1).
Why it’s dangerous
The product contains undeclared diclofenac, a prescription non-steroidal anti-inflammatory drug (NSAID), and chlorpheniramine, an over-the-counter antihistamine. These undeclared ingredients can cause serious adverse reactions, allergic responses, or dangerous drug interactions in users who did not intend to take them.
Who’s affected
Consumers who purchased Pyrola Advanced Joint Formula capsules, specifically those with the UPC 7 11746 00075 8, are affected. Individuals sensitive to NSAIDs or antihistamines, or those taking other medications that could interact with diclofenac, are at particular risk.
How to tell if you have this one
Look for a 60-count bottle of Pyrola Advanced Joint Formula capsules manufactured by GC Natural Nutrition, Inc., located in Fullerton, CA. The specific UPC code is 7 11746 00075 8. The recall applies to all lots.
- Brand
Pyrola- Product
PYROLA Advanced Joint Formula capsules, 60-count bottle, G & C Natural Nutrition Inc., Fullerton, CA 92833, UPC 7 11746- Category
Drug
What to do — step by step
Stop taking the product
Cease consumption of Pyrola Advanced Joint Formula capsules immediately due to the presence of undeclared prescription and over-the-counter drugs.
Check your bottle UPC
Verify if you have the recalled item by checking for UPC 7 11746 00075 8 on the packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-1330-2015 (June 12, 2015) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1330-2015 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 12, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.