Class II · Moderate risk Terminated
Rancheros sold under brand Heather's Choice
Reason Heather's Choice Rancheros is being recalled because the firm operated without a permit and lack a HACCP plan.
Salmon Chowder sold under brand Heather's Choice recall
Recalled by Heather's Choice · Anchorage, AK, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Heather's Choice Salmon Chowder is being recalled because the firm operated without a permit and lack a HACCP plan. This product also contains undeclared coconut.
Undeclared allergen: Fish
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
Salmon Chowder, sold under brand Heather's Choice. The product is labeled in parts: "***Salmon Chowder***HEATHER'S CHOICE***meals for adventuring***ingredients: salmon + peas + carrots + potatoes+ coconut milk powder***directions: cover food with hot water + let sit for 15 minutes***".
Quantity: 13 units
Food: Seafood & fish
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.
Expiration date: September 2015
Where it was sold
FDA's distribution note: sold interstate via internet sale from the website: http://www.heatherschoice.com
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 fish; 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
- Heather's Choice
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 1, 2014
- In FDA report of
- Nov 5, 2014
- Terminated
- Nov 25, 2014
- FDA recall number
- F-0097-2015 · event 69407
- 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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