CLASS I Food recall · Reported 13 Jan 2021 · FDA Enforcement Report
9" French Silk Base recalled by American Blue Ribbon Holdings
American Blue Ribbon Holdings is recalling 9" French Silk Base, distributed in 11 states. The recall was initiated on 22 Dec 2020 and the FDA has classified it as Class I.
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-0200-2021
- FDA event ID
- 87045
- Recalling firm
- American Blue Ribbon Holdings, Chaska, MN
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 22 Dec 2020
- FDA classified
- 7 Jan 2021
- Reported
- 13 Jan 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Tree Nuts
- Product category
- Other
Timeline
| 22 Dec 2020 | Recall initiated by company | |
| 7 Jan 2021 | Classified by FDA | +16 days |
| 13 Jan 2021 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Pecan
Product as listed by the FDA
9" French Silk Base, Item 7545, Count per case 6 Ea., Case Weight 12 lb. 3 oz. UPC 50796220075458. Keep Frozen.
Where it was distributed
Pies shipped to two distributors who shipped to Village Inn Restaurants located in the following states: AR, AZ, IA, IL, KS, MN, MO, ND, NE, OK, and WY.
ArkansasArizonaIowaIllinoisKansasMinnesotaMissouriNorth DakotaNebraskaOklahomaWyoming
Questions about this recall
Why was it recalled?
Undeclared Pecan
Which lots are affected?
Lot Code Printed on the side of the pie tin: CH20322CPS (Hour)(Minute) 7545 Case Label CH20326FSK
Where was it sold?
Pies shipped to two distributors who shipped to Village Inn Restaurants located in the following states: AR, AZ, IA, IL, KS, MN, MO, ND, NE, OK, and WY.
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 I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
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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