📍Recalling firmGrato Holdings, Inc.201 Apple Blvd · Woodbine, IA 51579-1503
✎ GovInfoNow plain-language explainer
Grato Holdings, Inc. is recalling B-Force Homeopathic 1 Fl Oz (30 mL) bottles distributed by BioActive Nutritional, Inc. The product was recalled because it was labeled as 'superpotent.' This specific recall involves 1,480 bottles distributed in Florida. Read more at govinfonow.com/recall/36115-b-force-homeopathic-recall-superpotent-labeling-error.
“B-Force Homeopathic Recall: Superpotent Labeling Error.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/36115-b-force-homeopathic-recall-superpotent-labeling-error. Based on FDA recall #D-0653-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0653-2021%22&limit=1).
The FDA announced on June 18, 2021, that Grato Holdings, Inc. voluntarily recalled B-Force Homeopathic bottles due to superpotent labeling errors. The recall affects 1,480 units distributed in Florida.
The product is labeled as homeopathic but contains superpotent levels of active ingredients. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show Grato Holdings, Inc. has issued eight other recalls since December 22, 2015. Recent brand recalls include an Energique Mineral Magic product recalled on May 3, 2024, for microbial contamination risk and a V-FORCE Homeopathic product recalled on October 30, 2023, for incorrect active ingredient formulation. Other recent recalls of similar products include a Gasco Isopropyl Alcohol 70% recall (May 29, 2026) and an Xyvona (Levorphanol) 2mg Tablet recall (May 22, 2026).
How to tell if you have this one
Look for B-Force Homeopathic in a 1 Fl Oz (30 mL) bottle with NDC 43857-0576-1 and Lot number Z61917. These items were distributed by BioActive Nutritional, Inc. in Melbourne, FL.
Brand
B-Force
Category
Drug
Where it went and when
Where it was distributed
Distributed in Florida.
Listed by the agency
Not listed
FDA distribution: “FL” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida.
Recall timeline
FDA terminated this recall 16 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0653-2021 (June 18, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0653-2021 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 10, 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.