Lower riskFood recall · FDA · Published April 19, 2019
Glorybee Raw California Orange Blossom Honey Recall: Unapproved Fumagillin Residue
Glorybee recalls 18oz jars of Raw California Orange Blossom Honey due to unapproved fumagillin antibiotic residue found in FDA samples. Consumers should avoid using this product.
“Glorybee Raw California Orange Blossom Honey Recall: Unapproved Fumagillin Residue.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17559-glorybee-raw-california-orange-blossom-honey-recall-unapproved-fumagillin-residue. Based on FDA recall #F-1349-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1349-2019%22&limit=1).
Glorybee Natural Sweeteners, Inc. voluntarily recalled Item #13898 Raw California Orange Blossom Honey due to unapproved fumagillin residue, according to the FDA on April 19, 2019.
How to tell if you have it
Brand: Glorybee
Product: Item #13898 Raw California Orange Blossom Honey
Packaging: 18 oz jar with gold metal lid
Retail Jar UPC: 0 30042 00305 9
Lot codes: MG0117488, MG0129500
Units affected: 3162 jars
The hazard
Two random FDA samples tested for unapproved fumagillin, an antibiotic drug, residue. The recall is classified as Class III.
Context
GovInfoNow's records show other recent recalls include Bee Well Honey (2026-03-20), 52USA Popping Boba (2026-04-13), and Dakota Honey Spreadable Spun Honey (2026-04-04).
How to tell if you have this one
Look for 18oz jars with gold metal lids and the UPC 0 30042 00305 9 or 0 30042 00338 7. The product label reads 'Raw Honey California ORANGE BLOSSOM' with no best by date.
Brand
Glorybee
Product
Item #13898 Raw California Orange Blossom Honey, packaged in an 18 oz jar with gold metal lid. Retail Jar UPC: 0 30042
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Product
Discard any recalled honey jars immediately to avoid potential health risks.
Where it went and when
Where it was distributed
Distributed in 9 states.
Listed by the agency
Not listed
FDA distribution: “distributed in CA, CO, FL, GA, IL, NY, OR, TX, and WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Florida, Georgia, Illinois, New York, Oregon, Texas, Washington.
Recall timeline
FDA terminated this recall 2 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 #F-1349-2019 (April 19, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1349-2019 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.