Nestle Nesquik Chocolate Flavor, chocolate beverage powder, New Wt 48.7 OZ. Product labeling…
Recalling firm: Nestle USA
Possible metal fragments
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: Aug 2, 2012.
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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
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Full FDA record and distribution details
Original product description
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***".
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| batch | 210458802G | Recalled product under following Batch number: 210458802G, 210558802G, 210758803G, 210658801g, 210658801G. Code Date Breakdown: 2-Year code (2012) 104-Julian code 5880-pl |
| batch | 210558802G | 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- |
| batch | 210658801g | alled 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 |
| batch | 210758803G | 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-lin |
Original FDA recall reason
Firm initiated recall due to potential contamination with metal fragments.
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.
Data updated September 16, 2026. View official FDA data ↗
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