La Flor ground COMINO recall
Recalled by La Flor Products Co., Inc. · Hauppauge, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may contain undeclared peanut protein.
Undeclared allergen: Peanut
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
La Flor ground COMINO, 1) NET WT. 2 OZ, 2) NET WT 6 OZ (170.1g), 3) NET WT. 5 LBS. Packed By La Flor Products Co., Inc., Hauppauge, NY 11788 Tel 631-851-9601. http://www.laflor.com
Quantity: 1401 Total cases (1103 cases/12 units/2 oz, 258 cases/12 units/6 oz, 40 cases/4 units/5 lb)
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 # RLF800, Expiration Dates for the following Products: 1) 5/13/18 & 7/14/18, Product 2) 5/14/18 and Product 3) 6/16/18.
Where it was sold
Connecticut Massachusetts New Jersey New York Pennsylvania Rhode Island Washington
FDA's distribution note: CT, NY, NJ, RI, PA, Washington D.C. & MA
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. The risk from an undeclared allergen is to people allergic to peanut; 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
- La Flor Products Co., Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jan 12, 2015
- In FDA report of
- Feb 18, 2015
- Terminated
- Jun 8, 2018
- FDA recall number
- F-1039-2015 · event 70211
- Official record
- FDA enforcement report search