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Food FDA Class II Completed Foreign material

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

Nestle-USA, Inc. (Corporate Office) Published Apr 9, 2025

Risk level

Class II

May cause a temporary or reversible health problem; slight chance of serious harm.

Severity score 50/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Nestle-USA, Inc. (Corporate Office) or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Potential foreign material (wood-like material)

Hazards

Wood · primary

Affected products (1)

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

25485 cases

UPC: 013800558060, 00138005580770
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

Affected areas

AlabamaArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIllinoisIndianaIowaKansasKentuckyLouisianaMaineMarylandMassachusettsMichiganMinnesotaMissouriNebraskaNew HampshireNew YorkNorth CarolinaNorth DakotaOhioOklahomaOregonPennsylvaniaSouth CarolinaTennesseeTexasUtahVermontVirginiaWashingtonWisconsin

Timeline

  1. Initiated
    Mar 17, 2025
  2. Published
    Apr 9, 2025
Recall number
F-0683-2025
Agency
U.S. Food and Drug Administration
Country
US

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.