SLR Food Distribution Inc. Recalls Wise Wife Brand Ground Cinnamon Due To Elevated Lead Levels
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SLR Food Distribution Inc. is voluntarily recalling Wise Wife Brand Ground Cinnamon after testing found elevated lead levels. The affected 110-gram containers were distributed in 14 states from September 2025 through June 2026; no illnesses have been reported. Consumers should not use the product and can discard it or return it for a full refund.

SLR Food Distribution Inc. is recalling Wise Wife Brand Ground Cinnamon because it may contain elevated levels of lead, according to a company announcement published by the U.S. Food and Drug Administration on October 29, 2026. The recall covers a specific 110-gram (3.88-ounce) container sold in 14 states; the company says no illnesses have been reported.

The affected product is packaged in a clear plastic container with a black screw-top cap. Consumers can identify it by the UPC 0688474302754, printed on the back label, and the “Best Before” date 4/25/2027. The FDA notice identifies the product as ground cinnamon under the Wise Wife brand.

According to the announcement, the recalled cinnamon was distributed to retail and grocery stores in Connecticut, Indiana, Kansas, Massachusetts, Michigan, Minnesota, North Carolina, Nebraska, New York, Ohio, Pennsylvania, Texas, Virginia and Wisconsin. Distribution took place between September 8, 2025, and June 28, 2026. The notice does not specify how many containers were distributed or how many may remain available to consumers.

SLR said the recall began after a sample collected and analyzed by The Connecticut Agricultural Experiment Station showed elevated lead levels. The company is asking customers to stop selling and distributing the product, remove it from store shelves, and place any remaining inventory on hold while following its recall instructions. Consumers are advised not to eat the cinnamon; they may discard it or return it to the place of purchase for a full refund.

At a glance
announcementWhen: Announced and published by the FDA on O…
The developmentSLR Food Distribution recalled Wise Wife ground cinnamon after a sample tested by a Connecticut agricultural laboratory showed elevated lead levels.

Lead Risk in a Common Pantry Spice

The recall matters because ground cinnamon is often used in small quantities across many foods and drinks, and lead exposure can occur without obvious immediate symptoms. The company’s announcement says exposure to very low levels over a short period may not cause noticeable symptoms, and that an increase in blood lead levels may be the only apparent sign. That statement is general health information in the recall notice; it does not establish that any particular consumer has been exposed or harmed.

The notice describes potential health effects as dependent on the amount and duration of exposure, as well as a person’s age and body weight. It warns that prolonged exposure in children can damage the central nervous system and may lead to learning disorders, developmental defects and other long-term problems. These risks explain why consumers should check the identifying details and stop using the product even if it looks and smells normal.

For shoppers, the UPC, package size and best-before date provide practical ways to distinguish the recalled item from other cinnamon products. The distribution list also gives retailers and households in the named states a reason to check cupboards and stock. The FDA page says it posts company recall announcements as a public service and does not endorse the company or product.

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How the Recall Was Identified

The company attributes the recall to a sample tested by The Connecticut Agricultural Experiment Station. The FDA notice reports the result as elevated lead levels but does not provide a numerical test result, the laboratory’s threshold, or additional details about the sampling and analysis. The available information therefore supports the reported recall reason, but not a more specific estimate of exposure from an individual container.

The announcement was made by SLR Food Distribution Inc. of Hicksville, New York, and posted by the FDA on October 29, 2026. The distribution period began more than a year before the announcement and ended on June 28, 2026. The FDA describes the item as a food-and-beverage product in the spices, flavors and salts category, and the action as a company recall.

At the time of the announcement, no illnesses had been reported. That is the company’s reported status in the notice, not a statement that exposure was impossible. The release does not identify a specific lot number; it identifies the affected product using its UPC, package weight and best-before date.

““No illnesses have been reported to date.””

— SLR Food Distribution Inc., in the company announcement published by the FDA

Test Results and Exposure Details

The notice does not state the measured lead concentration, how many samples were tested, or whether testing found the same level across different containers. It also gives no estimate of how many units were sold, how much product remains in stores or homes, or whether further batches or related products are being assessed. The information provided does not establish that every container carries the same amount of lead.

It is also unclear whether any consumers have sought medical evaluation after using the cinnamon. SLR reported no illnesses to date, but the notice does not give details about consumer complaints or describe any health investigation. It does not say whether the FDA has conducted separate testing or issued findings beyond publishing the company announcement.

People who are concerned about possible exposure can contact a health care provider for advice, especially if a child may have consumed the product repeatedly. The recall notice does not provide a specific medical testing recommendation or individual risk assessment.

Consumer Returns and Retailer Action

Consumers should first check whether their cinnamon matches all the identifying information: Wise Wife brand, ground cinnamon, 110 g (3.88 oz), UPC 0688474302754 and a best-before date of 4/25/2027. If it does, the company says not to consume it. The product may be discarded or returned to the place of purchase for a full refund.

Retailers and other customers holding stock are instructed to stop distribution and sale, remove affected containers from shelves, hold remaining inventory and follow SLR’s recall instructions. The announcement does not give a separate deadline for those actions or describe a public reporting process for stores.

Consumers with questions can contact SLR Food Distribution Inc. at 1-516-437-3782 or slrusaorder@gmail.com. The company lists its address as 495 West John St., Hicksville, NY 11801, and its business hours as Monday through Friday, 9 a.m. to 5 p.m. Eastern Time. The public notice does not specify whether additional testing results or updates are expected.

Key Questions

Which Wise Wife cinnamon product is included in the recall?

The recall covers Wise Wife Brand Ground Cinnamon in a 110 g (3.88 oz) clear plastic container with a black screw-top cap. Check for UPC 0688474302754 and a best-before date of 4/25/2027.

Where was the recalled cinnamon distributed?

SLR says it was distributed to retail and grocery stores in Connecticut, Indiana, Kansas, Massachusetts, Michigan, Minnesota, North Carolina, Nebraska, New York, Ohio, Pennsylvania, Texas, Virginia and Wisconsin, from September 8, 2025, through June 28, 2026.

What should I do if I have the recalled product?

Do not consume it. The company says consumers may discard the cinnamon or return it to the place of purchase for a full refund. Contact SLR at 1-516-437-3782 or slrusaorder@gmail.com with questions.

Have any illnesses been reported?

SLR’s announcement says no illnesses had been reported when the notice was issued. The announcement does not provide further information about consumer exposure or medical evaluations.

Why was the product recalled?

The recall was initiated after a sample collected and analyzed by The Connecticut Agricultural Experiment Station showed elevated lead levels, according to the company announcement. The notice does not publish the measured concentration.

Source: fda.gov

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