Nestle Coffee-Mate Creamer Recalled for Manufacturing Error Causing Acidity
Nestle Professional is recalling specific lots of Coffee-Mate Original Liquid Creamer Singles due to a manufacturing error that causes the product to become acidic.
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, but the source text describes a manufacturing error causing acidity without reporting any illnesses, injuries, or specific high-risk pathogens, fitting the criteria for a moderate severity voluntary recall.
Plain-English summary
Nestle Professional is recalling 520 cases of Nestle Coffee-Mate Coffee Creamer, Original Flavor, packaged in 3/8 fl oz single-serve tubs. The recall was initiated on October 9, 2012, due to a manufacturing error that causes the creamer to become acidic.
The affected product is distributed in California. The 50-count boxes have a UPC code of 50000-351107, a production code of 214651186 with a timestamp from 2:30 to 3:34, and a best-by date of March 2013.
Consumers should check their inventory for these specific codes and dates. The source text does not provide specific instructions for disposal or return, but the recall is driven by a quality defect rather than a reported pathogen or injury.
The recalled product
- Product
- Nestle Coffee-Mate Coffee Creamer, Original Flavor, packaged as 3/8 fl oz single serve tubs.50 single serve tubs are packaged in a self dispensing fiberboard box. Four fiberboard boxes are packaged in a case.
- Manufacturer
- Nestle Professional
- Category
- Food — Dairy / Creamer
- Affected units
- 520
Distribution
Distributed in 1 state:
Related recalls
Same hazard · manufacturing error
See all →- HighTRIGEN proximal humeral nails are missing their distal holes
FDA (Devices) · 2026-06-24
- HighStraumann angled custom abutments made from wrong bar material
FDA (Devices) · 2026-04-01
- HighStraumann custom abutments made from wrong bar material after mix-up
FDA (Devices) · 2026-04-01
- HighMedtronic tissue stabilizer recalled after tubing was assembled in reverse
FDA (Devices) · 2026-03-04
- HighDASH COVID and flu tests may give a false negative result
FDA (Devices) · 2025-08-13