Icelandic Provisions Recalls Vanilla Skyr Cups Due to Coconut Mislabeling
Icelandic Provisions Inc. is recalling Vanilla Skyr cups that may contain coconut skyr yogurt. The recall addresses a labeling error regarding the product flavor.
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 involves a labeling error (coconut mislabeled as vanilla). While coconut is a common allergen, the source text does not explicitly state that the product failed to declare coconut as an allergen, only that the flavor was mislabeled. This fits the criteria for minor labeling errors or low-risk contamination.
Plain-English summary
Icelandic Provisions Inc. is recalling 1,884 cases (22,608 cups) of Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068. The recall is being conducted because cups containing coconut skyr yogurt may have been mislabeled as vanilla skyr yogurt.
The affected product has a code of AUG022018. The product was distributed in New York, New Jersey, Massachusetts, Texas, Maryland, Connecticut, New Hampshire, Maine, and Washington.
Consumers who purchased this product should check their inventory for the specific UPC and code. If the product matches the description, consumers should stop using it and contact the manufacturer for further instructions.
The recalled product
- Product
- Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC: 854074006068
- Manufacturer
- Icelandic Provisions Inc.
- Category
- Food — Dairy / Yogurt
- Hazard
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 (1)
- AUG022018
Distribution
Related recalls
Same hazard · mis labeling
See all →- HighByron White Herbal Supplement Recalled for Undeclared Walnut Allergen
FDA (Food) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02