Class IITerminatedVoluntary: Firm initiated
Shovel and Spoon LLC: food recall H-0307-2025
Shovel and Spoon LLC of Limington, ME recalled Middle East Coast brand Tahini Dip; NET WT: 6 OZ (170g); INGREDIENTS: TAHINI, ORGANIC LEMON JUICE, GARLIC, OLIVE OIL,… Reason: Product may be contaminated with spoilage organisms. The FDA listed it as Class II in its Enforcement Report dated Jul 30, 2025; distribution: Massachusetts, Maine, New Hampshire.
Record status as published: Terminated (terminated Feb 11, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Middle East Coast brand Tahini Dip; NET WT: 6 OZ (170g); INGREDIENTS: TAHINI, ORGANIC LEMON JUICE, GARLIC, OLIVE OIL, SEA SALT, ORGANIC TOASTED SESAME. CONTAINS SESAME; Locally Crafted by SHOVEL AND SPOON; UPC 8 60005 50281 3
- Product quantity
- 658 tubs
- Reason for recall
- Product may be contaminated with spoilage organisms.
- Codes, lots and dates on the package
- MECT1082 Best by: 6/26/25 MECT1083 Best By: 7/3/25
- Distribution pattern
- ME, NH, MA
- Recalling firm
- Shovel and Spoon LLC, Limington, ME
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jun 20, 2025 |
| Classified by the FDA | Jul 18, 2025 |
| Published in the Enforcement Report | Jul 30, 2025 |
| Terminated | Feb 11, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0307-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.