FDA recall, , Moderate risk
Pure Palm Medjool Dates
Pure Palm dates- Medjool Dates are mislabeled as Coconut Date Bites.
Recall ended Jun 30, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
PURE PALM C/O DVD of Coachella, California, recalled Pure Palm dates- Medjool Dates because the product is mislabeled as Coconut Date Bites. The label is predominantly green with white lettering in a clear plastic clamshell container, and the product is coconut covered, while the label is for regular date bites.
The recall began on April 1, 2026, and was added to the FDA's Enforcement Report on April 8, 2026. The product was distributed to a single Direct Account with multiple locations across Delaware, Pennsylvania, New Jersey, Maryland, and New York. The FDA classified the recall on April 29, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is yours affected?
Match the UPC and lot code listed under your product.
A UPC is the number printed under a barcode.
Pure Palm dates- Medjool Dates
- UPC
- 852160007005
- Lot code
- PP0576D1
Recall details
- Company began the recall
- Sold in
Product was distributed to a single Direct Account with multiple locations across several East Coast states including (Delaware, Pennsylvania, New Jersey, Maryland, New York)
- Company
- PURE PALM C/O DVDCoachella, California
- Hazard
- Labeling error
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98718
- Recall number
- H-0681-2026
- Quantity recalled
- 50 cases
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Listed on Recall Canary
Classified by FDA
Recall ended
Archived
Summary updated
