Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g) box UPC 0 15000 04608 8 and NET WT 1.5
Summary
The FDA issued a Class I for Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Banana NET WT 3.2 OZ (90g by Nestle-USA, Inc. (Corporate Office). Reason: Firm received complaints of infant choking..
Details
Source
Food Recall
External ID
F-0579-2025
Action Date
2025-03-05
Status
Terminated
Category
food
Product Description
Gerber 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 49413
Lot/Code Info: All lots
Quantity Affected: 34,652cs/5/1.59 oz boxes + 271,115cs/5/3.2 oz boxes
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, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI and Puerto Rico.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-31
Company
Arlington, VA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 20 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 I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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-0579-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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