Nestle Toll House Chocolate Chip Tub Recalled for Rubber Pieces
Nestle Toll House Chocolate Chip Tub is being recalled due to the potential presence of food-grade rubber pieces.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves the potential presence of foreign material (food-grade rubber) without reported injuries or illnesses, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Gerber Products Company dba Nestle Infant Nutrition is recalling Nestle Toll House Chocolate Chip Tub (80oz), UPC 050000009343. The recall is issued because of the potential presence of food-grade rubber pieces in the product.
The recall covers 1,322,591 cases of the product. Distribution was limited to consignees in the US. The affected batch codes are 9192, 9206, 9221, 9224, 9235, 9241, 9242, 9252, 9263, 9264, 9270, and 9271. The batch code date breakdown indicates a year of 2019 and a Julian date of 189.
Consumers should check their pantries for the specific UPC and batch codes listed above. If the product is found, consumers should stop using it and follow instructions from the recalling firm or the FDA regarding disposal or return.
The recalled product
- Product
- Nestle Toll House Chocolate Chip Tub (80oz), UPC 050000009343
- Category
- Food — Baking / Chocolate Chips
- Hazard
- Affected units
- 1,322,591
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (12)
- BATCH CODE(S): 9192
- 9206
- 9221
- 9224
- 9235
- 9241
- 9242
- 9252
- 9263
- 9264
- 9270
- 9271 Batch Code date Breakdown: YDDD Y-Year (2019) JJJ: Julian date (189)
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 26 recalled by Gerber Products Company dba Nestle Infant Nutrition under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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