CLASS I Food recall · Reported 16 Nov 2022 · FDA Enforcement Report
Bombolo Biscotti, Assorted Italian Cookies recalled by sotto i trulli
sotto i trulli is recalling Bombolo Biscotti, Assorted Italian Cookies. The recall was initiated on 19 Oct 2022 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-0136-2023
- FDA event ID
- 91046
- Recalling firm
- sotto i trulli, Sarasota, FL
- Brand
- Bombolo Biscotti
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 19 Oct 2022
- FDA classified
- 8 Nov 2022
- Reported
- 16 Nov 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Allergens
- Product category
- Cookies
Timeline
| 19 Oct 2022 | Recall initiated by company | |
| 8 Nov 2022 | Classified by FDA | +20 days |
| 16 Nov 2022 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared allergen: Walnuts
Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.
Product as listed by the FDA
Bombolo Biscotti, Assorted Italian Cookies, Net WT. 16 oz (454g)
Where it was distributed
Domestic distribution only.
Questions about this recall
Why was it recalled?
Undeclared allergen: Walnuts
Which lots are affected?
LOT #092222, Exp. Date 04/05/2023
Where was it sold?
Domestic distribution only.
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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