Recall Register

Food, drugs, devices › Nestle-USA, Inc. (Corporate Office)

Food recall: Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER P

FDA enforcement event 96226 · Class I · initiated 31 Jan 2025 · status Terminated · terminated 22 Jul 2025

FoodVoluntary: Firm initiated2 product recordsArlington, VA

Nestle-USA, Inc. (Corporate Office) (Arlington, VA) initiated this food recall on 31 Jan 2025; FDA lists 2 product records under event 96226, classified Class I.

FDA defines Class I as a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death. 37% of the 569 food enforcement events initiated in 2025 carry the same class.

Status: Terminated, terminated 22 Jul 2025. Initiation: voluntary: firm initiated. Nestle-USA, Inc. (Corporate Office) has 5 enforcement events on this register, with a median of 1 product record per event.

Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.

Recalling firm

Nestle-USA, Inc. (Corporate Office), Arlington, VA.

Reason for recall

"Firm received complaints of infant choking."

Distribution

"The products were shipped to distribution centers in the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY,…"

Product records

Recall numberProductQuantityClassStatusReport date
F-0578-2025Gerber 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 49413314,398cs/5/3.2 oz boxesClass ITerminated5 Mar 2025
F-0579-2025Gerber 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 4941334,652cs/5/1.59 oz boxes + 271,115cs/5/3.2 oz boxesClass ITerminated5 Mar 2025

Context

37%of 2025 food events are Class I569 events that year
2product records in this eventfirm median: 1
5events on this register for the firm

Other enforcement events for Nestle-USA, Inc. (Corporate Office)

InitiatedProduct (first record)TypeClassRecords
17 Mar 2025Lean Cuisine Lemon Garlic Shrimp Stir Fry, NET WT 10 OZ (283g), in a plastic tray with film seal, packaged inside a papeFoodClass II3
10 Aug 2023Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with plastFoodClass II1
3 Nov 2022Nestle Toll House Edible Chocolate Chip Cookie Dough packaged in 15oz tubs - 4 tubs per caseFoodClass II1
12 Oct 2022"***Nestle***STUFFED***CHOCOLATE CHIP COOKIE DOUGH***4 JUMBO COOKIES***NET WT 8 OZ***"FoodClass II1

All 5 events for Nestle-USA, Inc. (Corporate Office)

Questions and answers

Why was this food recalled?

FDA's record gives the reason for recall as: "Firm received complaints of infant choking."

What does Class I mean?

FDA classifies recalls by relative degree of health hazard. Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

Where was the product distributed?

FDA's distribution pattern field reads: "The products were shipped to distribution centers in the following states: AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NV, NY,…"

Is the recall still ongoing?

FDA lists the status as Terminated; the termination date is 22 Jul 2025. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.

Where does this data come from?

openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.

Provenance

Source: openFDA food enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.