Nutri-Dyn Calcium D-Glucarate Plus Recall: Mislabeling Risk
Nutri-Dyn recalls 60-capsule calcium glucarate supplement due to mislabeled bottles from Lot 160876. Consumers may have the product with UPC 7 13757-09611 9.
Lower-risk recall
During production of St. John's Wort, Lot 160876, a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus
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What happened, in plain English
Nutri-Dyn is recalling a specific calcium glucarate supplement because some bottles were mislabeled during production. This means some people might have the wrong product that could cause confusion about what they're taking. Read more at govinfonow.com/recall/21349-nutri-dyn-calcium-d-glucarate-plus-recall-mislabeling-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/21349-nutri-dyn-calcium-d-glucarate-plus-recall-mislabeling-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2423-2017
Cite this page
“Nutri-Dyn Calcium D-Glucarate Plus Recall: Mislabeling Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21349-nutri-dyn-calcium-d-glucarate-plus-recall-mislabeling-risk. Based on FDA recall #F-2423-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2423-2017%22&limit=1).
Why it’s dangerous
During production, some bottles of this supplement were mistakenly labeled as Calcium D-Glucarate Plus when they were actually St. John's Wort. This mislabeling could lead to confusion about which product someone is taking, potentially causing them to consume the wrong supplement.
Who’s affected
People who bought the Nutri-Dyn Calcium D-Glucarate Plus supplement with UPC 7 13757-09611 9 and lot number 160876 from October 2016 are affected. Those most at risk are individuals who take dietary supplements without checking labels carefully.
How to tell if you have this one
Check for the UPC code 7 13757-09611 9 and lot number 160876 on the bottle. The product was manufactured in October 2016.
- Brand
Nutri-Dyn- Product
Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 7 13757-09611 9 and lot number 160876 on the bottle to confirm if it's part of the recall.
Where it went and when
Where it was distributed
Distributed in 24 states, and outside the U.S.
FDA distribution: “US: AZ, CA, CO,, FL, IA, ID, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NV, NY, OH, PA SC, SC, TX, WI, WY. OUS: ISRAEL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Colorado, Florida, Idaho, Iowa, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska, Nevada, New Jersey, New York, North Carolina, North Dakota, Ohio, Pennsylvania, South Carolina, Texas, Wisconsin, Wyoming.
Recall timeline
FDA terminated this recall 4 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product dangerous to take?
No, the recall is due to mislabeling, not a safety hazard. The product itself is safe but could be confused with another supplement.
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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 #F-2423-2017 (May 12, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2423-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.