Label is predominantly green with white lettering in a clear plasti…
Recalled by PURE PALM C/O DVD
Food recall
PURE PALM C/O DVD
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
PURE PALM C/O DVD has recalled Label is predominantly green with white lettering in a clear plasti…, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 22, 2026 and was initiated on April 1, 2026. It is classified as a Class II recall, which means using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers Label is predominantly green with white lettering in a clear plasti…, with approximately 50 cases affected. The company behind the recall is PURE PALM C/O DVD, based in Coachella, CA. The FDA describes the product as: “Label is predominantly green with white lettering in a clear plastic clamshell container. Pure Palm dates- Medjool Dates Net Wt. 16OZ UPC: 852160007005”
Why was Label is predominantly green with white lettering in a clear plasti… recalled?
According to the FDA, the stated reason for the recall is: “mislabeled Coconut Date Bites. (product is coconut covered, label is for regular date bites).” In plain terms, this recall relates to an undeclared ingredient or allergen.
An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.
What should you do?
If you think you may have bought Label is predominantly green with white lettering in a clear plasti…, compare it against the product description and identifying codes (LOT CODE PP0576D1 BEST BY:02/26/2027) before using it. This recall is currently listed as ongoing.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact PURE PALM C/O DVD or your local health authority.
About this recall
This recall was distributed in CA. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Ongoing
- Date reported
- April 22, 2026
- Recall started
- April 1, 2026
- Distributed in
- CA
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was Label is predominantly green with white lettering in a clear plasti… recalled?+
According to the FDA: mislabeled Coconut Date Bites.
How serious is this recall?+
Class II — moderate. Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
What should I do if I have Label is predominantly green with white lettering in a clear plasti…?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0681-2026. Information last synced from the FDA on July 5, 2026.