Rikki USA Hollandaise Sauce Recall: Mold Risk in Refrigerated Tubs
Rikki USA recalls refrigerated Hollandaise sauce tubs with mold risk. Products sold as Sallere Classic Sauces and Butters from 2016. Consumers should check labels for lot #1640288.
Lower-risk recall
Hollandaise Sauce was recalled due to presence of mold.
Contact the company
What happened, in plain English
Rikki USA recalled refrigerated Hollandaise sauce tubs due to mold growth. This poses a health risk as mold can cause illness if consumed. Affected products were sold with specific labels and lot numbers. Read more at govinfonow.com/recall/23065-rikki-usa-hollandaise-sauce-recall-mold-risk-in-refrigerated-tubs.
Source Summary by GovInfoNow · govinfonow.com/recall/23065-rikki-usa-hollandaise-sauce-recall-mold-risk-in-refrigerated-tubs · Updated October 9, 2026 · FDA enforcement record: FDA #F-0377-2017
Cite this page
“Rikki USA Hollandaise Sauce Recall: Mold Risk in Refrigerated Tubs.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23065-rikki-usa-hollandaise-sauce-recall-mold-risk-in-refrigerated-tubs. Based on FDA recall #F-0377-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0377-2017%22&limit=1).
Why it’s dangerous
Mold growth in refrigerated Hollandaise sauce can lead to potential health issues if consumed. The sauce was sold in plastic tubs with a net weight of 7 ounces and a best-by date of November 22, 2016.
Who’s affected
Households using refrigerated Hollandaise sauce tubs labeled with lot #1640288 are affected. Those who have consumed the product may face health risks from mold exposure.
How to tell if you have this one
Check for plastic tubs labeled with 'HOLLANDAISE SAUCE' and lot number 1640288. Products were sold as Sallere Classic Sauces and Butters with a best-by date of November 22, 2016.
- Brand
Rikki USA- Category
Food
What to do — step by step
Check Product Label
Look for the lot number 1640288 on the plastic tub label.
Where it went and when
Where it was distributed
Distributed in Maryland and Oregon.
FDA distribution: “distributed in MD and OR.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Maryland, Oregon.
Recall timeline
FDA terminated this recall 34 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- FDA terminated the recall
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
Questions people ask
Is this product safe to eat?
The recall states mold was present, so the product is not safe to consume.
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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-0377-2017 (October 5, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0377-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.