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Oregon Potato Company LLC recall - IQF frozen Blueberry (30lbs. cases and 1400 lbs. totes), product of…
FDA (enforcement) · March 4, 2026 · Class I
- Oregon Potato Company LLC recalled IQF frozen Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is… - an FDA enforcement event posted , classified Class I, covering 1 product entry.
- FDA-stated reason: Listeria monocytogenes
- Details as of ; the linked official notice is authoritative for lot codes, VINs, and remedies.
- Agency
- FDA
- Posted
- Initiated
- Classification
- Class I
- Status
- Terminated
- Recalling firm
- Oregon Potato Company LLC
- Source ID
- 98435
FDA Enforcement Report search →
How this recall compares
- Oregon Potato Company LLC has 4 recall events in the FDA (2012+) and USDA-FSIS (2014+) records tracked here; by posting date this is the 4th. The one before it: Oregon Potato Company recall - Rader Farms Organic Fresh Start Smoothie… ().
- It is one of 4 Listeria recall events FDA and USDA-FSIS posted in March 2026 (all Listeria recalls).
Other recalls from Oregon Potato Company LLC
| Posted | Agency | Recall | Class |
|---|---|---|---|
| FDA | Oregon Potato Company recall - Rader Farms Organic Fresh Start Smoothie Blueberry,… | Class I | |
| FDA | Oregon Potato Company recall - Frozen whole Red Raspberries; packed in a 12 oz.… | Class II | |
| FDA | Oregon Potato Company recall - IQF 1/4 x 1/4 Yellow Onion Dice, item number 102654, bulk… | Class I |
Matched by company name after removing suffixes such as Inc. and LLC; parent companies and subsidiaries are counted separately.
Product entries (1)
| Recall # | Product | Codes / lots | Distribution |
|---|---|---|---|
| H-0522-2026 | IQF frozen Blueberry (30lbs. cases and 1400 lbs. totes), product of USA. Product is packaged in polyethylene bag within a corrugated 30lbs. case or packaged… | Lot codes on 30 lbs. CASES: 2055 B2, 2065 B1, and 2065 B3. Lot codes on 1400 lbs. TOTES:… | Distributed in MI, OR, WA, WI and in Canada. |
FDA enforcement entries have no per-recall public URL - verify via the FDA Enforcement Report search using the firm name or a recall number above.
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