Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 g) UPC 4 056489 34380 6. Frozen product.
Summary
The FDA issued a Class II for Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 g) UPC 4 056489 34380 6. Fro by Frozen Food Development Inc. Reason: Possible contamination of Listeria monocytogenes in frozen chopped spinach..
Details
Source
Food Recall
External ID
F-0735-2022
Action Date
2022-02-23
Status
Terminated
Category
food
Product Description
Steamable by Lidl Chopped Spinach NET WT 12 OZ (340 g) UPC 4 056489 34380 6. Frozen product.
Lot/Code Info: R17742 Best Buy Date 9/10/23 and R17963 Best Buy Date 9/10/23
Quantity Affected: Unknown
Reason for Recall
Possible contamination of Listeria monocytogenes in frozen chopped spinach.
Distribution
Distributed to Lidl stores VA, MD, NC, SC, GA, NJ, NY, and PA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-19
Company
Rheems, PA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Frozen Food Development Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Frozen Food Development Inc have FDA actions?
This is the only FDA action we have on record for Frozen Food Development Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0735-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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