Taylor Farms Fruit & Cheese Recall: Wood Slivers Risk
Taylor Farms recalls 6oz fruit & cheese products due to potential wood slivers in the product. Consumers should stop using affected items to avoid injury.
Use caution until it’s fixed
The firm was notified that an ingredient used to manufacture the recalled product may contain wood slivers.
Contact the company
What happened, in plain English
Taylor Farms is recalling 6-ounce fruit and cheese products that may contain wood slivers. This could cause injury if the slivers cut the user during consumption. Read more at govinfonow.com/recall/20408-taylor-farms-fruit-cheese-recall-wood-slivers-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/20408-taylor-farms-fruit-cheese-recall-wood-slivers-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0022-2018
Cite this page
“Taylor Farms Fruit & Cheese Recall: Wood Slivers Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20408-taylor-farms-fruit-cheese-recall-wood-slivers-risk. Based on FDA recall #F-0022-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0022-2018%22&limit=1).
Why it’s dangerous
Wood slivers can be present in the product during manufacturing. If the slivers are ingested, they could cause cuts or injuries to the mouth or throat.
Who’s affected
Anyone who purchased Taylor Farms Wawa Fruit & Cheese products with the specific lot numbers listed in the recall. People who eat the product are most at risk of injury from wood slivers.
How to tell if you have this one
Check for the product name 'Wawa Fruit & Cheese', 6oz (170g) in a rigid plastic clamshell container. Look for lot numbers TFNJ244 through TFNJ264 with sell-by dates from September 6-26, 2017.
- Brand
Taylor Farms- Category
Food
What to do — step by step
Stop Using Product
Immediately stop using any recalled Wawa Fruit & Cheese products that may contain wood slivers.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “Product is distributed to Pennsylvania, New Jersey, Delaware, Maryland, and Virginia, Florida.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Delaware, Florida, Maryland, New Jersey, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 3.9 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-0022-2018 (September 21, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0022-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.