CLASS I Food recall · Reported 3 May 2023 · FDA Enforcement Report
3610100 Blackberry IQF recalled by Patagonia Food
Patagonia Food is recalling 3610100 Blackberry IQF, distributed in California, Nebraska, Nevada, Oregon, Texas, Washington. The recall was initiated on 17 Mar 2023 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-0760-2023
- FDA event ID
- 91941
- Recalling firm
- Patagonia Food, San Luis Obispo, CA
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 17 Mar 2023
- FDA classified
- 24 Apr 2023
- Reported
- 3 May 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Hepatitis A
- Product category
- Fish
Timeline
| 17 Mar 2023 | Recall initiated by company | |
| 24 Apr 2023 | Classified by FDA | +38 days |
| 3 May 2023 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Possible Hepatitis A in blackberries
Product as listed by the FDA
Patagonia Foods 3610100 Blackberry IQF Product of Mexico Net Wt. 30 LBS. (13.61 kg) Production/Lot Code 20422 Distributed By: Patagonia Foods, LLC. San Luis Obispo, CA 93401 patagoniafoods.com
Where it was distributed
U.S. distribution to the following: CA, OR, NE, TX, WA, NV No foreign distribution.
Questions about this recall
Why was it recalled?
Possible Hepatitis A in blackberries
Which lots are affected?
Lot Code: 20422
Where was it sold?
U.S. distribution to the following: CA, OR, NE, TX, WA, NV 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 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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