CLASS II Food recall · Reported 17 Oct 2018 · FDA Enforcement Report
Signature Reserve Bourbon Maple Blondie Ice Cream recalled by Albertsons
Albertsons is recalling Signature Reserve Bourbon Maple Blondie Ice Cream, distributed in Oregon, Washington. The recall was initiated on 26 Sep 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-0019-2019
- FDA event ID
- 81125
- Recalling firm
- Albertsons, Boise, ID
- Brand
- Signature Reserve
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 26 Sep 2018
- FDA classified
- 5 Oct 2018
- Reported
- 17 Oct 2018
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Allergens
- Product category
- Ice Cream & Frozen Desserts
Timeline
| 26 Sep 2018 | Recall initiated by company | |
| 5 Oct 2018 | Classified by FDA | +9 days |
| 17 Oct 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
Undeclared allergen; tree nuts.
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
Signature Reserve Bourbon Maple Blondie Ice Cream 14 FL OZ UPC 2113009912
Where it was distributed
U.S. distribution to the following: OR and WA No foreign distribution.
Stores named: Albertsons
Questions about this recall
Why was it recalled?
Undeclared allergen; tree nuts.
Which lots are affected?
BB Aug 12, 19 Plt 04-116 (6)
Where was it sold?
U.S. distribution to the following: OR and WA No foreign distribution.
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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