CLASS I Food recall · Reported 8 Feb 2023 · FDA Enforcement Report
James Farm Frozen Red Raspberries recalled by Exportadora Copramar Ltda
Exportadora Copramar Ltda is recalling James Farm Frozen Red Raspberries, distributed in 8 states. The recall was initiated on 3 Dec 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-0319-2023
- FDA event ID
- 91262
- Recalling firm
- Exportadora Copramar Ltda, Linares, N/A
- Brand
- James
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 3 Dec 2022
- FDA classified
- 27 Jan 2023
- Reported
- 8 Feb 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Hepatitis A
- Product category
- Raspberries
Timeline
| 3 Dec 2022 | Recall initiated by company | |
| 27 Jan 2023 | Classified by FDA | +55 days |
| 8 Feb 2023 | 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
Product may be contaminated with Hepatitis A Virus.
Product as listed by the FDA
James Farm brand Frozen Red Raspberries; 2-5lb Bags; NET WT 10 LB (4.5 kg); KEEP FROZEN; IQF; Individually Quick Frozen; FOR FOOD SERVICE SALE ONLY; Distributed by: RD/JET, LLC; 15-24 132nd Street, College Point, NY 11356; Country of Origin: CHILE.
Where it was distributed
NY, NJ, CT, MA, RI, PA, M, VA, DE
ConnecticutDelawareMassachusettsNew JerseyNew YorkPennsylvaniaRhode IslandVirginia
Questions about this recall
Why was it recalled?
Product may be contaminated with Hepatitis A Virus.
Which lots are affected?
BEST IF USED BY JUN/14/2024 UPC: 76069501010 Lot Code: CO 22-165/CO 22-165-1
Where was it sold?
NY, NJ, CT, MA, RI, PA, M, VA, DE
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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