Check the Batch
Class ITerminated in FDA datasetRecall initiated Nov 8, 2012

Nesquik Chocolate Powder, 1) 6x40.7oz

Recalling firm: Nestle USA

Why it was recalled

Nestle is recalling Nesquik Chocolate Powder because certain lots of its ingredients, calcium carbonate, may be contaminated with Salmonella.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 23, 2013.

Check your package

Compare the exact product and package details with the label you have.

ProductNesquik Chocolate Powder, 1) 6x40.7oz, UPC 0 28000 68230 9. 2) 12x21.8oz, UPC 0 28000 68090 9. 3) 12x10.9oz, UPC 0 28000 67990 3.
Package size7oz
UPC028000679903, 028000680909, 028000682309

FDA code information

Production codes: 1) 2282574810 and 2282574820. 2)2278574810, 2278574820, 2279574810, 2279574820, 2284574820, 2284574830, 2285574810, 2285574820, 2287574820, 2289574810, 2289574820. 3) 2278574810.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Nesquik Chocolate Powder, 1) 6x40.7oz, UPC 0 28000 68230 9. 2) 12x21.8oz, UPC 0 28000 68090 9. 3) 12x10.9oz, UPC 0 28000 67990 3.

Extracted codes and context

TypeCode / valueContext
UPC0280006799037oz, UPC 0 28000 68230 9. 2) 12x21.8oz, UPC 0 28000 68090 9. 3) 12x10.9oz, UPC 0 28000 67990 3.
UPC028000680909Nesquik Chocolate Powder, 1) 6x40.7oz, UPC 0 28000 68230 9. 2) 12x21.8oz, UPC 0 28000 68090 9. 3) 12x10.9oz, UPC 0 28000 67990 3.
UPC028000682309Nesquik Chocolate Powder, 1) 6x40.7oz, UPC 0 28000 68230 9. 2) 12x21.8oz, UPC 0 28000 68090 9. 3) 12x10.9oz, UPC 0 28000 67990 3.

Original FDA recall reason

Nestle is recalling Nesquik Chocolate Powder because certain lots of its ingredients, calcium carbonate, may be contaminated with Salmonella.

Recall details

Recall number
F-0737-2013
Event ID
63672
FDA status
Terminated
Initiated
Nov 8, 2012
Reported
Dec 5, 2012
Classified
Nov 27, 2012
Terminated
Jan 23, 2013
Quantity
18,768 units total
Location
Glendale, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Nationwide in the US

FDA source record · F-0737-2013

Data updated September 16, 2026. View official FDA data ↗

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