LA PASTA Dairy-Free Mushroom Ravioli
Reason The product is labeled as gluten-free, but contains gluten.
HEINEN'S Potato Gnocchi * Preservative Free * recall
Recalled by La Pasta, Inc. · Silver Spring, MD, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
LA PASTA, INC has initiated a recall of Heinen's Potato Gnocchi 9 oz. , because of a undeclared milk allergen .
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
HEINEN'S Potato Gnocchi * Preservative Free * 9 oz. (225 g) in clear film plastic trays
Quantity: 208 cases
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#1119-1120 / 1121-1122 / 1132-1133 / 2016-2017 / 2027-2028 / 2034-2035 / 2038-2039 / 2130-2131 / 2139-2140 / 2221-2222 / 2231-2232.
Where it was sold
Illinois Ohio
FDA's distribution note: The product was distributed to the following states IL and OH
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 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
- La Pasta, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 21, 2018
- In FDA report of
- Mar 14, 2018
- Terminated
- May 11, 2018
- FDA recall number
- F-0909-2018 · event 79322
- Official record
- FDA enforcement report search