Harris Teeter Mama Biscotti Mini Biscotti Recall: Undeclared Almonds Allergen
Harris Teeter recalls Mama Biscotti Mini Biscotti, Triple Chocolate with undeclared almonds. Consumers should check UPC 7203670827 and lot 17338 for affected items.
Lower-risk recall
Undeclared allergen: Almonds
Contact the company
What happened, in plain English
Harris Teeter is recalling Mama Biscotti Mini Biscotti, Triple Chocolate due to undeclared almonds. This poses a risk for people with almond allergies. The recall affects specific lot numbers and UPC codes. Read more at govinfonow.com/recall/19894-harris-teeter-mama-biscotti-mini-biscotti-recall-undeclared-almonds-allergen.
Source Summary by GovInfoNow · govinfonow.com/recall/19894-harris-teeter-mama-biscotti-mini-biscotti-recall-undeclared-almonds-allergen · Updated October 7, 2026 · FDA enforcement record: FDA #F-0521-2018
Cite this page
“Harris Teeter Mama Biscotti Mini Biscotti Recall: Undeclared Almonds Allergen.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19894-harris-teeter-mama-biscotti-mini-biscotti-recall-undeclared-almonds-allergen. Based on FDA recall #F-0521-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0521-2018%22&limit=1).
Why it’s dangerous
The product contains undeclared almonds, which can cause allergic reactions in sensitive individuals. This is a food safety issue for people with almond allergies.
Who’s affected
People with almond allergies are at risk. This recall affects Harris Teeter's Mama Biscotti Mini Biscotti, Triple Chocolate with specific UPC and lot numbers.
How to tell if you have this one
Check for the UPC 7203670827 and lot number 17338 on the packaging. The product is sold under Harris Teeter's HT Traders brand.
- Brand
Harris Teeter- Product
Harris Teeter's HT Traders Mama Biscotti Mini Biscotti, Triple Chocolate, UPC: 7203670827- Category
Food
What to do — step by step
Check Product Label
Look for the UPC 7203670827 and lot number 17338 on the packaging.
Where it went and when
Where it was distributed
Distributed in 6 states and D.C..
FDA distribution: “DE, FL, MD, NC, SC, VA and Washington, DC.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Delaware, District of Columbia, Florida, Maryland, North Carolina, South Carolina, Virginia.
Recall timeline
FDA terminated this recall 35 days 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-0521-2018 (December 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0521-2018 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.