McShare's Premark HS Vitamin RDA Premix Recall: Soy Not Declared on Label
McShare's Inc recalls Premark HS Vitamin RDA Premix (50 lbs) due to soy not being declared on label. This may pose a risk for people with soy allergies. Consumers should check their product labels and contact the company for details.
Lower-risk recall
Product manufactured with an ingredient that contains low levels of soy; soy is not declared on product label.
Contact the company
What happened, in plain English
McShare's Inc is recalling Premark HS Vitamin RDA Premix (50 lbs) because it contains soy that isn't listed on the label. This could be a problem for people with soy allergies who might react to the hidden soy. Read more at govinfonow.com/recall/22006-mcshare-s-premark-hs-vitamin-rda-premix-recall-soy-not.
Source Summary by GovInfoNow · govinfonow.com/recall/22006-mcshare-s-premark-hs-vitamin-rda-premix-recall-soy-not · Updated October 8, 2026 · FDA enforcement record: FDA #F-1863-2017
Cite this page
“McShare's Premark HS Vitamin RDA Premix Recall: Soy Not Declared on Label.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22006-mcshare-s-premark-hs-vitamin-rda-premix-recall-soy-not. Based on FDA recall #F-1863-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1863-2017%22&limit=1).
Why it’s dangerous
The product contains soy that isn't declared on the label. This means people with soy allergies could potentially react to the soy if they consume it. The risk is low because the soy is present in small amounts and not intended for human consumption.
Who’s affected
People who have soy allergies are most at risk from this recall. The product is sold to farmers and livestock feed businesses.
How to tell if you have this one
Check for the product name 'Premark HS Vitamin RDA Premix', net weight 50 lbs, and item number 136375. The lot number is HSRDA-290616-50 with an expiration date of June 29, 2017.
- Brand
McShare's- Category
Food
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class III- Status
Terminated- Distribution
Product was distributed for further manufacturing to customers in MO and TX.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| F-1862-2017 | iXL Advanced Performance Matrix, Nutritional Premix, Net Wt. 50 lbs., Item No. 136375.; Lot numbers and Expiration dates: IXL-180516-20, 5/18/2017 IXL-180516-21, 5/18/2017 IXL-210117-50, 1/21/2018 | 3600 lbs. |
| F-1863-2017 | Premark HS Vitamin RDA Premix, Net Wt. 50 lbs., Item No. 136375.; Lot number and Expiration date: HSRDA-290616-50, 6/29/17 | 700 lbs |
What to do — step by step
Check Product Label
Look for the product name, net weight, and item number on the label to confirm if it's the recalled item.
Where it went and when
Where it was distributed
Distributed in Missouri and Texas.
FDA distribution: “Product was distributed for further manufacturing to customers in MO and TX.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Missouri, Texas.
Recall timeline
FDA terminated this recall 41 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- 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-1863-2017 (March 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1863-2017 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.