Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray with film seal, packaged inside a paperboa
Summary
The FDA issued a Class II for Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray wi by Nestle-USA, Inc. (Corporate Office). Reason: Potential foreign material (wood-like material).
Details
Source
Food Recall
External ID
F-0683-2025
Action Date
2025-04-09
Status
Completed
Category
food
Product Description
Lean Cuisine Spinach Artichoke Ravioli, NET WT 9 OZ (255g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
Lot/Code Info: Batch: 4311595912, Best By: DEC2025; Batch: 5002595912, Best By: FEB2026; Batch: 5037595912, Best By: MAR2026; Batch: 5064595912, Best By: APR2026; Product Number: 12340870; Unit UPC: 013800558060; Case UPC: 00138005580770
Quantity Affected: 25485 cases
Reason for Recall
Potential foreign material (wood-like material)
Distribution
Distributors and retailers in the following states: AL, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NE, NH, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-17
Company
Arlington, VA
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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Nestle-USA, Inc. (Corporate Office) has 8 FDA actions in our database, including 8 recalls.
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 (Nestle-USA, Inc. (Corporate Office)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Nestle-USA, Inc. (Corporate Office) have FDA actions?
Nestle-USA, Inc. (Corporate Office) has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0683-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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