Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap.

The Maros Group, LLC has recalled Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap., according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on April 8, 2026 and was initiated on November 5, 2025. 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 Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap., with approximately 2 cases/12 bottles per case affected. The company behind the recall is The Maros Group, LLC, based in Phoenix, AZ. The FDA describes the product as: “Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap.”

Why was Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap. recalled?

According to the FDA, the stated reason for the recall is: “Undeclared milk.” 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 Prickly Pear Jelly. 9 oz (268 g) glass bottle with gold cap., compare it against the product description and identifying codes (lot code: 2250416 Sell by date: 042326 (April 23, 2026) 053026 (May 30, 2026) 061126 (June 11, 2026) Lot code: 2250616 Sell by Date: 061126 (June 11, 2026)) before using it.

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 The Maros Group, LLC or your local health authority.

About this recall

This recall was distributed in AZ. 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.