WTI DV All Natural 35lb Food Recall: Wood Pieces Found
WTI recalls DV All Natural 35lb food due to wood pieces found in some lots. Consumers should check lot numbers and contact WTI for details.
Lower-risk recall
Foreign matter, wood pieces, were found in the product.
Contact the company
What happened, in plain English
WTI is recalling its DV All Natural 35-pound food product because wood pieces were found in some batches. This could cause injury if eaten, so affected consumers should stop using the product. Read more at govinfonow.com/recall/23475-wti-dv-all-natural-35lb-food-recall-wood-pieces-found.
Source Summary by GovInfoNow · govinfonow.com/recall/23475-wti-dv-all-natural-35lb-food-recall-wood-pieces-found · Updated October 9, 2026 · FDA enforcement record: FDA #F-2100-2016
Cite this page
“WTI DV All Natural 35lb Food Recall: Wood Pieces Found.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23475-wti-dv-all-natural-35lb-food-recall-wood-pieces-found. Based on FDA recall #F-2100-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2100-2016%22&limit=1).
Why it’s dangerous
Wood pieces can be accidentally ingested when eating the food, which may cause injury. The hazard is not life-threatening but could cause minor harm if swallowed.
Who’s affected
Anyone who purchased WTI DV All Natural 35lb food with lot numbers JF-005747 through JF-005799. People who eat the product are at risk of injury from ingesting wood pieces.
How to tell if you have this one
Check the lot numbers on the product label: JF-005747, JF-005748, JF-005751, JF-005752, JF-005758, JF-005776, JF-005778, JF-005787, JF-005795, or JF-005799.
- Brand
WTI- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers on the label: JF-005747, JF-005748, JF-005751, JF-005752, JF-005758, JF-005776, JF-005778, JF-005787, JF-005795, or JF-005799.
Stop Using Product
If the product has a recalled lot number, stop using it immediately to avoid potential injury from ingesting wood pieces.
Where it went and when
Where it was distributed
Distributed in Illinois, and outside the U.S.
FDA distribution: “IL and Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA terminated this recall 10 months 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-2100-2016 (August 10, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2100-2016 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.