CLASS II Food recall · Reported 9 Dec 2015 · FDA Enforcement Report
Doria Authentic Italian Goodness, Amaretti Biscuits recalled by Bauli
Bauli is recalling Doria Authentic Italian Goodness, Amaretti Biscuits, distributed in New York. The recall was initiated on 27 Oct 2015 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-0340-2016
- FDA event ID
- 72526
- Recalling firm
- Bauli, Castel D' Azzano
- Brand
- Doria Authentic
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 27 Oct 2015
- FDA classified
- 2 Dec 2015
- Reported
- 9 Dec 2015
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Product category
- Citrus
Timeline
| 27 Oct 2015 | Recall initiated by company | |
| 2 Dec 2015 | Classified by FDA | +36 days |
| 9 Dec 2015 | Published 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
Bauli S.p.A. has initiated a recall due to high levels of Aflatoxin B1
Product as listed by the FDA
Doria AUTHENTIC ITALIAN GOODNESS, Amaretti BISCUITS, Net Wt. 8.81 oz (250g), UPC 799540801696, BAULI S.p.A Via Verdi, 31 37060 Castel d'Azzano (VR) Stabilimento di Via Pontebbana, 32 Orsago (Treviso) Italia. PRODUCT OF ITALY
Where it was distributed
NY
Questions about this recall
Why was it recalled?
Bauli S.p.A. has initiated a recall due to high levels of Aflatoxin B1
Which lots are affected?
Lot codes: LD79 & LD80
Where was it sold?
NY
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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