Sun Opta Soy Bits Recall: Plastic Pieces in Roasted Soy Bits
Sun Opta recalls 1450 pounds of Soy Bits and 1400-1600 pounds of Soy Splits due to plastic pieces found in roasted soy bits. Consumers should check lot numbers 34217037 and 34217043.
Stop using this now
Pieces of plastic were found in roasted soy bits.
Contact the company
What happened, in plain English
Sun Opta is recalling organic, roasted soy bits and soy splits that contain plastic pieces. This hazard could cause choking or injury if ingested, so affected consumers should stop using the product immediately. Read more at govinfonow.com/recall/21931-sun-opta-soy-bits-recall-plastic-pieces-in-roasted-soy.
Source Summary by GovInfoNow · govinfonow.com/recall/21931-sun-opta-soy-bits-recall-plastic-pieces-in-roasted-soy · Updated October 8, 2026 · FDA enforcement record: FDA #F-2084-2017
Cite this page
“Sun Opta Soy Bits Recall: Plastic Pieces in Roasted Soy Bits.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21931-sun-opta-soy-bits-recall-plastic-pieces-in-roasted-soy. Based on FDA recall #F-2084-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2084-2017%22&limit=1).
Why it’s dangerous
Plastic pieces can be accidentally swallowed or inhaled, leading to choking or internal injuries. The hazard is present in the roasted soy bits and soy splits that were sold in specific lot numbers.
Who’s affected
Anyone who purchased Sun Opta's Soy Bits or Soy Splits with lot numbers 34217037 or 34217043. Children and individuals with small mouths are at higher risk due to the choking hazard.
How to tell if you have this one
Check the product label for lot numbers 34217037 or 34217043. The product is sold in individual Super Sacs and includes organic, roasted soy bits and soy splits.
- Brand
Sun Opta- Category
Food
What to do — step by step
Stop Using Now
Immediately stop using the recalled soy bits or soy splits if they have lot numbers 34217037 or 34217043.
Where it went and when
Where it was distributed
Distributed in Idaho and Minnesota.
FDA distribution: “ID and MN.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Idaho, Minnesota.
Recall timeline
FDA terminated this recall 14 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.
Similar recalls
Latest food recalls
Keep exploring
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-2084-2017 (March 23, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2084-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.