Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl…
Recalled by 529 Commerce, LLC (Rooted in RARE)
Classification pending
The agency has not yet assigned a severity class to this recall. Classification usually follows the initial announcement by several weeks — check the official notice for the latest status.
529 Commerce, LLC (Rooted in RARE) has recalled Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl…, according to the U.S. Food and Drug Administration (FDA). The recall was announced on July 30, 2026. The FDA has not yet assigned it a severity classification — that usually follows the initial announcement by several weeks.
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 Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl…. The company behind the recall is 529 Commerce, LLC (Rooted in RARE). The FDA describes the product as: “Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) flexible foil pouches”
Why was Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl… recalled?
According to the FDA, the stated reason for the recall is: “Undeclared egg allergen. Aquafaba is normally a plant-based egg substitute, so shoppers buying it are often specifically avoiding eggs, including people with an egg allergy who could have a serious reaction.” 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 Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl…, compare it against the product description and identifying codes (Check the 4 oz (113 g) and 12 oz (340 g) foil pouches. If you have an egg allergy, do not use this product. Return it for a refund or discard it.) 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 529 Commerce, LLC (Rooted in RARE) or your local health authority.
About this recall
This recall was distributed in United States. 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 most to anyone with a food allergy or sensitivity to the ingredient that wasn't listed on the label. For everyone else this product is generally safe to eat — the danger is specific to people avoiding that ingredient, who had no way to know it was there.
Distribution listed in the notice: United States.
What undeclared ingredient or allergen actually means
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.
In this case, the concern applies specifically to Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl… from 529 Commerce, LLC (Rooted in RARE) — not to the wider category of products. Similar items from other brands aren't part of this recall.
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: Check the 4 oz (113 g) and 12 oz (340 g) foil pouches. If you have an egg allergy, do not use this product. Return it for a refund or discard it.
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 529 Commerce, LLC (Rooted in RARE) or your local health department.
Full recall details
- Status
- Ongoing
- Date reported
- July 30, 2026
- Distributed in
- United States
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 Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl… recalled?+
According to the FDA: Undeclared egg allergen.
How serious is this recall?+
Classification pending. The agency has not yet assigned a severity class to this recall. Classification usually follows the initial announcement by several weeks — check the official notice for the latest status.
What should I do if I have Rooted in RARE Aquafaba Powder in 4 oz (113 g) and 12 oz (340 g) fl…?+
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: FDA-PR-AQUAFABA-2026. Information last synced from the FDA on July 31, 2026.