Why it was recalled
LA PASTA, INC has initiated a recall of Heinen's Potato Gnocchi 9 oz. , because of a undeclared milk allergen .
Product description
HEINEN'S Potato Gnocchi * Preservative Free * 9 oz. (225 g) in clear film plastic trays
Lot numbers, UPCs & expiration codes
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
The product was distributed to the following states IL and OH
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0909-2018
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Feb 21, 2018
- FDA report date
- Mar 14, 2018
- Quantity
- 208 cases
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- La Pasta, Inc.
Original FDA data
Every field from FDA enforcement report F-0909-2018, exactly as published.
Show all FDA fields
- City
- Silver Spring
- State
- MD
- Status
- Terminated
- Country
- United States
- Event ID
- 79322
- Address
- 2727 Pittman Dr
- Code information
- LOT#1119-1120 / 1121-1122 / 1132-1133 / 2016-2017 / 2027-2028 / 2034-2035 / 2038-2039 / 2130-2131 / 2139-2140 / 2221-2222 / 2231-2232.
- Postal code
- 20910-1807
- Report date
- Mar 14, 2018
- Product type
- Food
- Recall number
- F-0909-2018
- Classification
- Class I
- Recalling firm
- La Pasta, Inc.
- Product quantity
- 208 cases
- Termination date
- May 11, 2018
- Reason for recall
- LA PASTA, INC has initiated a recall of Heinen's Potato Gnocchi 9 oz. , because of a undeclared milk allergen .
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- HEINEN'S Potato Gnocchi * Preservative Free * 9 oz. (225 g) in clear film plastic trays
- Distribution pattern
- The product was distributed to the following states IL and OH
- Recall initiation date
- Feb 21, 2018
- Initial firm notification
- Center classification date
- Mar 8, 2018