“Hu Chocolate-Covered Hunks Sour Goldenberries Recall: Undeclared Almonds.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14779-hu-chocolate-covered-hunks-sour-goldenberries-recall-undeclared-almonds. Based on FDA recall #F-0337-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0337-2021%22&limit=1).
Hu Products LLC voluntarily recalled chocolate-covered hunk sour goldenberries due to undeclared almonds, the FDA said on March 5, 2021. Consumers should check their products for affected lot codes.
How to tell if you have it
Brand: Hu
Product: CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES Net Wt. 4 oz (113g) in black bag
UPC: 00850180006510
Master Case GTIN: 10850180006517
Lot #: 202891
Best By: 08/2021
Sold in NV, IL, MD, NJ, TX, PA, OR, IA
The hazard
The product may contain undeclared almonds. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Hu Products has two other recalls on record since Oct. 2, 2020. Other recent recalls of similar products include Fran's PureBar Almondmilk Chocolate (Dec. 20, 2025), High Valley Orchard Chocolate Covered Raisins (June 24, 2026), and H-E-B Strawberry Yogurt Alternative (Dec. 17, 2025).
How to tell if you have this one
Check for the black bag packaging with a 4oz (113g) net weight. The affected lot number is 202891 and batch date is 08/2021.
Brand
Hu
Product
Hu***CHOCOLATE-COVERED HUNKS SOUR GOLDENBERRIES***Net Wt. 4 oz (113g); packaged in a black bag; Distributed by: Hu
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the lot number 202891 and batch date 08/2021 on the black bag packaging.
Where it went and when
Where it was distributed
Distributed in 8 states.
Listed by the agency
Not listed
FDA distribution: “NV, IL, MD, NJ, TX, IL, PA, OR, IA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Iowa, Maryland, Nevada, New Jersey, Oregon, Pennsylvania, Texas.
Recall timeline
FDA published this recall 12 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
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-0337-2021 (March 5, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0337-2021 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 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.