CLASS III Food recall · Reported 9 Nov 2016 · FDA Enforcement Report

Hollandaise Sauce, sold as Sallere Classic Sauces recalled by Rikki USA

Rikki USA is recalling Hollandaise Sauce, sold as Sallere Classic Sauces and Butters, refrigerated product, distributed in Maryland, Oregon. The recall was initiated on 5 Oct 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot # 1640288. Best by: 11-22-2016
Quantity recalled125 cases (or 750/7 oz. tubs total)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0377-2017
FDA event ID
75390
Recalling firm
Rikki USA, Redmond, WA
Classification
Class III
Status
Terminated
Recall initiated
5 Oct 2016
FDA classified
2 Nov 2016
Reported
9 Nov 2016
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Mold
Product category
Sauces & Condiments

Timeline

5 Oct 2016Recall initiated by company
2 Nov 2016Classified by FDA+28 days
9 Nov 2016Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Hollandaise Sauce was recalled due to presence of mold.

Product as listed by the FDA

Hollandaise Sauce, sold as Sallere Classic Sauces and Butters, refrigerated product. Each plastic tub has a net wt 7 oz. The label is read in parts: "***HOLLANDAISE SAUSE***Use on chicken, seafood and vegetables***.

Where it was distributed

distributed in MD and OR.

MarylandOregon

Questions about this recall

Why was it recalled?

Hollandaise Sauce was recalled due to presence of mold.

Which lots are affected?

Lot # 1640288. Best by: 11-22-2016

Where was it sold?

distributed in MD and OR.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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