Lemon Pesto Sauce
Reason Lemon Pesto Sauce recalled because parmesan cheese is declared but milk is not declared on label.
Classic Pesto Sauce recall
Recalled by Salsa Dianne · Union, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Classic Pesto Sauce (with a twist) is recalled because Parmesan cheese is declared but milk is not declared on label.
Undeclared allergen: Milk
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Classic Pesto Sauce (with a twist), net wt. 4 oz. (113 g). Product is packaged in a round Styrofoam containers with translucent plastic lid. The UPC is 8 20103 77214 3. The product is labeled in parts: "***Classic Pesto (with a twist)***INGREDIENTS: Olive Oil, Brazil nuts, Garlic, Parmesan cheese, Basil, Onion***Made & Packaged by Dianne's Kitchen***Union, Oregon 97883***".
Quantity: firm did not provide
Food: Sauces, dips & dressings
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.
best if used (or frozen) by 4/30/2016
Where it was sold
Oregon
FDA's distribution note: distributed in Oregon
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. The risk from an undeclared allergen is to people allergic to milk; for anyone else the product is generally not a safety concern. 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
- Salsa Dianne
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 7, 2016
- In FDA report of
- May 18, 2016
- Terminated
- May 24, 2016
- FDA recall number
- F-1322-2016 · event 73803
- 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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