Class IIITerminated in FDA datasetJun 27, 2012

Nestle Nesquik Chocolate Flavor, chocolate beverage powder, New Wt 48.7 OZ. Product labeling reads in part:"***Nestle Nesquick Chocolate FLAVOR*** NET WT***48.7OZ***

Recalling firm: Nestle USA

Why it was recalled

Firm initiated recall due to potential contamination with metal fragments.

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The exact product

Nestle Nesquik Chocolate Flavor, chocolate beverage powder, New Wt 48.7 OZ. Product labeling reads in part:"***Nestle Nesquick Chocolate FLAVOR*** NET WT***48.7OZ***DISTRIBUTED BY***NESTLE USA, INC., GLENDALE, CA 91203 USA***".

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Recalled product under following Batch number: 210458802G, 210558802G, 210758803G, 210658801g, 210658801G. Code Date Breakdown: 2-Year code (2012) 104-Julian code 5880-plant code 2-shift G-line designation

TypeCode / valueContext
batch210458802GRecalled product under following Batch number: 210458802G, 210558802G, 210758803G, 210658801g, 210658801G. Code Date Breakdown: 2-Year code (2012) 104-Julian code 5880-pl
batch210558802GRecalled product under following Batch number: 210458802G, 210558802G, 210758803G, 210658801g, 210658801G. Code Date Breakdown: 2-Year code (2012) 104-Julian code 5880-plant code 2-
batch210658801galled product under following Batch number: 210458802G, 210558802G, 210758803G, 210658801g, 210658801G. Code Date Breakdown: 2-Year code (2012) 104-Julian code 5880-plant code 2-shift G-line designatio
batch210758803GRecalled product under following Batch number: 210458802G, 210558802G, 210758803G, 210658801g, 210658801G. Code Date Breakdown: 2-Year code (2012) 104-Julian code 5880-plant code 2-shift G-lin

Recall details

Recall number
F-1811-2012
Event ID
54145
FDA status
Terminated
Initiated
Jun 27, 2012
Reported
Aug 8, 2012
Classified
Jul 27, 2012
Terminated
Aug 2, 2012
Quantity
405 cases at 6 per case
Location
Glendale, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Distributed to distributor and retail in US State of TX.

FDA source record · F-1811-2012

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

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.