Recalls You Should Know About Week of October 7, 2018


We’ve rounded up a list of recalls issued by the US Food and Drug Administration (FDA) and the US Department of Agriculture (USDA) from this past week.

We’ve rounded up a list of recalls issued by the US Food and Drug Administration (FDA) and the US Department of Agriculture (USDA) from this past week.

Ladyfingers Catering, LLC Issues Recall for Country Ham Rolls Potentially Contaminated with Listeria monoctyogenes

Ladyfingers Caterers is voluntarily recalling its Signature Shaved Country Ham Rolls as a result of the Johnston County Hams recall. The rolls were made with ham produced by Johnston County Hams, which recently initiated a recall of its ham products due to possible contamination with Listeria monocytogenes.

The product was distributed between April 3, 2017 through October 3, 2018 to retail stores in California, District of Columbia, Delaware, North Carolina, New York, South Carolina and Virginia.

There has been one reported illness for this recall.

For more information about this recall, check out the recall statement.

Bazzini LLC, Recalls Pistachio Products Linked to Salmonella Contamination

Bazzini LLC of Allentown, PA out of an abundance of caution, is recalling 4,000 pounds of Roasted and Salted Colossal Natural, Super Colossal Natural and Rams Head Natural In Shell Pistachios received from one of its suppliers because it has the potential to be contaminated with Salmonella.

The affected product was distributed through retail sale, direct delivery, and mail order in New York, New Jersey, Vermont, Massachusetts, Washington DC, and Virginia.

No other products are affected by this recall.

To learn more about the affected product, check out the news release.

Eight and Company LLC (Sprayology) Recalls Homeopathic Aqueous-Based Products With Potential Microbial Contamination

Eight and Company LLC, d/b/a Sprayology is voluntarily recalling all lots within expiry from 10/18-7/22 of its aqueous-based homeopathic product line for human use. All products manufactured by the contract manufacturer, King Bio, have been recalled due to possible microbial contamination.

Eight and Company LLC, d/b/a Sprayology has not to date received any reports of adverse events related to this recall.

The products are for assorted symptom relief can be identified by the main label on the bottle and by the expiration date printed on the backside of the label. Each product recalled is an individual 1.38 oz. oral spray in white bottle manufactured at the King Bio, Inc. facility in Asheville, NC. Product was distributed nationwide via wholesale, retail and online sales.

To read more about this recall check out the company’s statement.

Malone’s Fine Sausage Inc, Recalls Products Potentially Contaminated with Listeria monocytogenes

Malone’s Fine Sausage Inc., a Milwaukee, Wis. establishment, is recalling approximately 26,323 pounds of ready-to-eat pork head cheese product that may be adulterated with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The ready-to-eat pork head cheese items were produced on various dates from Aug. 27, 2018 through Oct. 5, 2018.

The products subject to recall bear establishment number “EST. 15702” inside the USDA mark of inspection. These items were shipped to retail locations in Illinois, Michigan and Wisconsin and were also sold via internet catalog sales.

The problem was discovered on Oct. 9, 2018 by FSIS inspection program personnel while verifying the disposition of product that FSIS tested positive for Listeria monocytogenes.

To learn about the recalled products, check out the USDA’s announcement.

Liveyon, LLC Recalls Regen Series Products Due to Possible Adverse Reactions

Liveyon, LLC (“Liveyon”) is a distributor of stem cell products manufactured by Genetech, Inc. (“Genetech”), a laboratory located in San Diego, CA. Liveyon marketed and distributed these products under the trade name ReGen Series.

Liveyon has voluntarily recalled all ReGen Series® products due to reported possible adverse reactions.

The Center for Biologics Evaluation and Research (CBER), a division of the Food & Drug Administration (FDA), which oversees human cells and tissue-based products, contacted Liveyon on Thursday, September 28, 2018. CBER stated concerns related to the products manufactured by Genetech and informed Liveyon of reported possible adverse reactions due to the use of the ReGen Series product.

Liveyon immediately suspended shipment of all product pending an inquiry by CBER into the source of the adverse reactions. In addition, Liveyon voluntarily recalled any Genetech products it may have distributed.

Liveyon will resume distribution of the new product line effective Monday, October 8, 2018.

To learn more about this recall, consult the company’s statement.

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