Nestle-USA, Inc. (Corporate Office) FDA recall records

The FDA has published 8 food recall enforcement records naming Nestle-USA, Inc. (Corporate Office) between 2022 and 2025, covering 5 separate recall events. The firm is recorded in Virginia. Data last updated 2 September 2026.

Records of 29,386
8
Share of all recalls
0%
Class I of 8
2
Reported between
2022 to 2025

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 8 records cover 5 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

2 of these records are Class I, 6 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

What was recalled for

A single record can name more than one hazard, so these counts overlap.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 8 records.
ReportedProductFirmReasonClass
2025-04-09Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a paperboard carton; 10 consumer units per caseNestle-USA, Inc. (Corporate Office)Potential foreign material (wood-like material)Class II
2025-04-09Lean 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 caseNestle-USA, Inc. (Corporate Office)Potential foreign material (wood-like material)Class II
2025-04-09Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per caseNestle-USA, Inc. (Corporate Office)Potential foreign material (wood-like material)Class II
2025-03-05Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.59 oz box UPC 0 15000 01015 7 GERBER PRODUCTS CO., FREMONT, MI 49413Nestle-USA, Inc. (Corporate Office)Firm received complaints of infant choking.Class I
2025-03-05Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER PRODUCTS CO., FREMONT, MI 49413Nestle-USA, Inc. (Corporate Office)Firm received complaints of infant choking.Class I
2023-09-13Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with plastic overwrap, 12 packages per case, Keep RefrigeratedNestle-USA, Inc. (Corporate Office)Potential presence of wood fragments.Class II
2022-12-14Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per caseNestle-USA, Inc. (Corporate Office)Potential of foreign material within product.Class II
2022-10-26"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"Nestle-USA, Inc. (Corporate Office)Consumer complaints reported presence of white pieces of plastic in cookie product.Class II

Questions

How many FDA recalls has Nestle-USA, Inc. (Corporate Office) had?
The FDA has published 8 food recall enforcement records naming Nestle-USA, Inc. (Corporate Office) between 2022 and 2025. Those records cover 5 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.