CLASS II Food recall · Reported 31 Aug 2022 · FDA Enforcement Report
Goat Cheese, Fresh Goat Cheese, Wasabi and logs recalled by Capriole
Capriole is recalling Goat Cheese, Fresh Goat Cheese, Wasabi and logs, distributed in Illinois, Indiana, Kentucky. The recall was initiated on 28 Jul 2022 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-1579-2022
- FDA event ID
- 90706
- Recalling firm
- Capriole, Greenville, IN
- Brand
- Goat
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 28 Jul 2022
- FDA classified
- 24 Aug 2022
- Reported
- 31 Aug 2022
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Allergens
- Product category
- Cheese
Timeline
| 28 Jul 2022 | Recall initiated by company | |
| 24 Aug 2022 | Classified by FDA | +27 days |
| 31 Aug 2022 | 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
Undeclared ingredients including blue #1 and yellow#5
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
Capriole Goat Cheese, Fresh Goat Cheese, Wasabi 5 pound and 8oz logs
Where it was distributed
KY, IL, IN
Questions about this recall
Why was it recalled?
Undeclared ingredients including blue #1 and yellow#5
Which lots are affected?
224140 227050 222150 226250 229060 228160
Where was it sold?
KY, IL, IN
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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