Schwan's Sea Salt Caramel Cashew Ice Cream Recall: Potential Glass Contamination
Schwan's recalls Sea Salt Caramel Cashew Ice Cream (206) due to potential glass contamination. Consumers should check product code for affected items.
Use caution until it’s fixed
One date of production of Schwan's Sea Salt Caramel Cashew Ice Cream is being due to potential glass contamination.
Contact the company
What happened, in plain English
Schwan's is recalling Sea Salt Caramel Cashew Ice Cream (product #206) because a batch may contain glass fragments. This could cause injury if the ice cream is consumed. Read more at govinfonow.com/recall/18080-schwan-s-sea-salt-caramel-cashew-ice-cream-recall-potential.
Source Summary by GovInfoNow · govinfonow.com/recall/18080-schwan-s-sea-salt-caramel-cashew-ice-cream-recall-potential · Updated October 5, 2026 · FDA enforcement record: FDA #F-0703-2019
Cite this page
“Schwan's Sea Salt Caramel Cashew Ice Cream Recall: Potential Glass Contamination.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/18080-schwan-s-sea-salt-caramel-cashew-ice-cream-recall-potential. Based on FDA recall #F-0703-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0703-2019%22&limit=1).
Why it’s dangerous
Glass fragments in the ice cream could cause cuts or lacerations if ingested. The contamination likely occurred during manufacturing, as the product was produced in a specific batch.
Who’s affected
Anyone who purchased Schwan's Sea Salt Caramel Cashew Ice Cream (product #206) with a production date code starting with '188211' is affected. Children and those with sensitive digestive systems are at higher risk.
How to tell if you have this one
Check the bottom of the carton for a product code starting with '188211' next to the large '206'. The affected product has a net weight of 56 ounces.
- Brand
Schwan's- Category
Food
What to do — step by step
Check Product Code
Look for a code starting with '188211' next to the large '206' on the bottom of the carton.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0703-2019 (November 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0703-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.