Publix Artichoke Spinach Dip Recall: Glass Fragments Risk
Publix recalls 16oz artichoke spinach dip due to potential glass fragments. Consumers should check UPC 000-41415-15961 and use by date May 16.
Stop using this now
Product may contain glass fragments
Contact the company
What happened, in plain English
Publix is recalling artichoke and spinach dip that may contain glass fragments. This could cause injury if the dip is consumed. Consumers should stop using the product and check the UPC code. Read more at govinfonow.com/recall/21370-publix-artichoke-spinach-dip-recall-glass-fragments-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/21370-publix-artichoke-spinach-dip-recall-glass-fragments-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2386-2017
Cite this page
“Publix Artichoke Spinach Dip Recall: Glass Fragments Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21370-publix-artichoke-spinach-dip-recall-glass-fragments-risk. Based on FDA recall #F-2386-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2386-2017%22&limit=1).
Why it’s dangerous
The dip may contain glass fragments that could cause cuts or lacerations if ingested. This is a serious hazard because glass can be sharp and difficult to detect in food.
Who’s affected
Anyone who purchased the 16-ounce plastic clamshell dip from Publix Super Markets. Children and those with sensitive mouths are at higher risk of injury.
How to tell if you have this one
Look for the 16-ounce plastic clamshell dip with UPC 000-4:41415-15961. Check the use by date: May 16 A1 and May 16 C1.
- Brand
Publix- Category
Food
What to do — step by step
Stop Using Now
Immediately stop using the dip if it has the UPC 000-41415-15961 and use by date May 16.
Where it went and when
Where it was distributed
Distributed in 6 states.
FDA distribution: “Distributed to the following states: AL, FL, GA, NC, SC, TN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alabama, Florida, Georgia, North Carolina, South Carolina, Tennessee.
Recall timeline
FDA terminated this recall 5.1 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-2386-2017 (May 8, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2386-2017 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.