Sokol and Co Solo Almond Paste Recall: Plastic and Metal Pieces Found
Sokol and Co recalls 6/7 LB Solo Almond Paste cans due to plastic and metal pieces found in product. Consumers should check lot number 16278 for affected items.
Lower-risk recall
Pieces of plastic and metal discovered within product.
Contact the company
What happened, in plain English
Sok: Sokol and Co is recalling 6/7 LB Solo Almond Paste cans because plastic and metal pieces were found inside the product. This could cause injury if the pieces are ingested. Read more at govinfonow.com/recall/22992-sokol-and-co-solo-almond-paste-recall-plastic-and-metal.
Source Summary by GovInfoNow · govinfonow.com/recall/22992-sokol-and-co-solo-almond-paste-recall-plastic-and-metal · Updated October 9, 2026 · FDA enforcement record: FDA #F-0427-2017
Cite this page
“Sokol and Co Solo Almond Paste Recall: Plastic and Metal Pieces Found.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/22992-sokol-and-co-solo-almond-paste-recall-plastic-and-metal. Based on FDA recall #F-0427-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0427-2017%22&limit=1).
Why it’s dangerous
The product contains plastic and metal pieces that could be ingested if the product is consumed. This poses a risk of injury, particularly for children who might accidentally swallow small pieces.
Who’s affected
Anyone who purchased the Solo Almond Paste cans with lot number 16278 from Sokol and Co. People who consume the product are most at risk of injury from ingesting plastic or metal pieces.
How to tell if you have this one
Check for Solo Almond Paste cans with a net weight of 42 lbs (19.09 kg) and lot number 16278. The product was sold by Sokol and Co.
- Brand
Sokol and Co- Category
Food
What to do — step by step
Check Product Lot Number
Look for the lot number 16278 on the can to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed in 3 states.
FDA distribution: “MA, MI, TX” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Massachusetts, Michigan, Texas.
Recall timeline
FDA terminated this recall 2.5 years 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-0427-2017 (October 21, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0427-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.