Lotsa Pasta International Food Shop Fresh Basil Infused Olive Oil
Reason Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.
Lotsa Pasta International Food Shop Roasted Garlic Infused Olive Oil recall
Recalled by Hale inc · Louisville, KY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Potential to be contaminated with Clostridium botulinum. Products manufactured without an approved process filed.
Pathogen: Botulism
Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Lotsa Pasta International Food Shop Roasted Garlic Infused Olive Oil, Net Wt. 12 oz. (375ml), packaged in a glass bottle, UPC 736211448415, packed 12 bottles per case
Quantity: 54 bottles (TOTAL)
Food: Pasta, rice & grains
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
No codes applied
Where it was sold
Kentucky
FDA's distribution note: KY
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Hale inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 9, 2025
- In FDA report of
- Dec 10, 2025
- Terminated
- May 7, 2026
- FDA recall number
- H-0240-2026 · event 97901
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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