Matiz Piparra Peppers are packaged in a clear glass jar
Reason A shard of glass being found in one of the jars.
Valencian Almonds FS Skinless recall
Recalled by Power Selles Imports dba Culinary Collective · Lynnwood, WA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential contamination with peanut while label does not declare peanut.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt. 352 oz./22 lb. (2 bags @ 11 lb.). UPC 5 901234 123457. Ingredients: Valencian Almonds, sunflower oil, sea salt and antioxidants (mixed tocopherols and rosemary extract to preserve freshness). IMPORTED BY CULINARY COLLECTIVE. May contain traces of peanuts, tree nuts, soy, milk, and milk derivatives.
Quantity: 78 cases
Food: Nuts & seeds
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.
Lot 38/41, Production date 9/23/21, best by date of 09/23/23.
Where it was sold
Colorado Montana New York Oregon
FDA's distribution note: Distributed in CO, MT, NY, and OR.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Power Selles Imports dba Culinary Collective
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 5, 2022
- In FDA report of
- May 18, 2022
- Terminated
- Jul 19, 2022
- FDA recall number
- F-1058-2022 · event 90145
- Official record
- FDA enforcement report search
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