Mehadrin Chocolate Leben
Recalled by UPSTATE NIAGARA COOPERATIVE
Food recall
UPSTATE NIAGARA COOPERATIVE
Class II — moderate
Using this product might cause a temporary or medically reversible health problem. The chance of serious harm is low.
UPSTATE NIAGARA COOPERATIVE has recalled Mehadrin Chocolate Leben, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on September 2, 2026 and was initiated on August 10, 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 Mehadrin Chocolate Leben, with approximately 3,975 cases affected. The company behind the recall is UPSTATE NIAGARA COOPERATIVE, based in Lancaster, NY. The FDA describes the product as: “Mehadrin Chocolate Leben; 6 OZ (170g) CUPS, UPC: 070784023144”
Why was Mehadrin Chocolate Leben recalled?
According to the FDA, the stated reason for the recall is: “Product may have been improperly pasteurized.”
What should you do?
If you think you may have bought Mehadrin Chocolate Leben, compare it against the product description and identifying codes (Lot code: 101426 L5 2W Use by date: 10/14/26) 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 UPSTATE NIAGARA COOPERATIVE or your local health authority.
About this recall
This recall was distributed in NY. 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.
Who this recall affects
This recall matters to anyone who bought Mehadrin Chocolate Leben. Even if you feel fine, it's worth checking what you have on hand rather than assuming you were missed.
Distribution listed in the notice: NJ.
How to check whether you have it
On packaged food, lot codes and best-by dates are usually printed in small date-coding ink on the side seam, the bottom of the package, or near the top seal — not on the front label. The UPC barcode is on the back or bottom.
Compare what you find against the identifying details in this recall: Lot code: 101426 L5 2W Use by date: 10/14/26
What to do if you already bought it
Do not eat the product, even if it looks and smells normal — contamination is usually invisible.
Return it to the store for a refund, or throw it away in a sealed bag so pets and wildlife can't reach it.
If it touched other food or surfaces, wash those surfaces and your hands with hot soapy water. When in doubt, contact UPSTATE NIAGARA COOPERATIVE or your local health department.
Full recall details
- Status
- Ongoing
- Date reported
- September 2, 2026
- Recall started
- August 10, 2026
- Distributed in
- NY
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 Mehadrin Chocolate Leben recalled?+
According to the FDA: Product may have been improperly pasteurized.
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 Mehadrin Chocolate Leben?+
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-1332-2026. Information last synced from the FDA on September 7, 2026.