CLASS II Food recall · Reported 12 Dec 2018 · FDA Enforcement Report
Vanilla Whipped Icing Artifically Flavored Product Number recalled
Rich Products is recalling Vanilla Whipped Icing Artifically Flavored Product Number: 09076, distributed nationwide in the US. The recall was initiated on 8 Nov 2018 and the FDA has classified it as Class II.
Check your package
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-0680-2019
- FDA event ID
- 81564
- Recalling firm
- Rich Products, Buffalo, NY
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 8 Nov 2018
- FDA classified
- 30 Nov 2018
- Reported
- 12 Dec 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Other
Timeline
| 8 Nov 2018 | Recall initiated by company | |
| 30 Nov 2018 | Classified by FDA | +22 days |
| 12 Dec 2018 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Possible contamination with cleaning chemicals.
Product as listed by the FDA
VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 09076 / UPC: 10049800090764
Where it was distributed
Nationwide
Questions about this recall
Why was it recalled?
Possible contamination with cleaning chemicals.
Which lots are affected?
10/8/18 case code is Best If Used By 03/31/2020 12878281; 10/9/18 is Best If Used By 04/01/2020 12878282o; 10/10/18 is Best If Used By 04/02/2020 12878283o; 10/11/18 is Best If Used By 04/03/2020 1287284
Where was it sold?
Nationwide
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 II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
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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