RecallHawk
Class I Recall

IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corru

Oregon Potato Company LLC

Summary

The FDA issued a Class I for IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is pac by Oregon Potato Company LLC. Reason: Listeria monocytogenes.

Details

Source

Food Recall

External ID

H-0522-2026

Action Date

2026-03-04

Status

Ongoing

Category

food

Product Description

IQF Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corrugated 30lbs. case or packaged in polyethylene liner within a Gaylord 1400lbs. tote. Product was not sold to consumers from retail stores. Willamette Valley Fruit Company 2994 82nd Ave. NE Salem OR 97305

Lot/Code Info: Lot codes on 30 lbs. CASES: 2055 B2, 2065 B1, and 2065 B3. Lot codes on 1400 lbs. TOTES: 3305 A1 and 3305 B1. Expiration dates or best-by date: 2055 B2 expiration 7/23/2027 2065 B1 expiration 7/24/2027 2065 B3 expiration 7/24/2027 3305 A1 expiration 11/25/2027 3305 B1 expiration 11/25/2027

Quantity Affected: 55,689 lbs.

Reason for Recall

Listeria monocytogenes

Distribution

Distributed in MI, OR, WA, WI and in Canada.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-02-12

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Oregon Potato Company LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Oregon Potato Company LLC have FDA actions?

This is the only FDA action we have on record for Oregon Potato Company LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0522-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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