C&T Produce Wholesale Inc., doing business as L&V Food Supply, the importer of record, is recalling approximately 1,152 pounds of ineligible peppered frozen, dried Siluriformes, or catfish products, that were produced by an establishment in Vietnam that is not eligible to export catfish to the United States, according to a Department of Defense All Food and Drug Activity message sent Feb. 25.

ZB Importing LLC is voluntarily recalling certain lots of six varieties of Ulker Brand snack rolls, biscuits, and wafers due to undeclared wheat, egg and/or milk in the ingredient list according to a Department of Defense All Food and Drug Activity message sent Feb. 25.

Kayco is recalling their Glicks Dark Chocolate Conettos product because it may contain undeclared milk according to a Department of Defense All Food and Drug Activity message sent Feb. 25.

Kedake Inc. is recalling two-pound packages of Las Ollas Botana mix snacks, because they may contain undeclared sesame, soy, wheat, yellow no 5, yellow no 6 and red no 6, according to a Department of Defense All Food and Drug Activity message sent Feb. 24.

One Source Nutrition, Inc. is voluntarily recalling all lots of Vitality capsules, due to the potential presence of sildenafil and tadalafil which are ingredients in FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors, according to a Department of Defense All Food and Drug Activity message sent Feb. 24.

Gerber Products Company is initiating a recall and discontinuation of all batches of Gerber® Soothe N Chew® Teething Sticks, due to a potential choking hazard for babies and young children, according to a Department of Defense All Food and Drug Activity message sent Feb. 2.

Wismettac Asian Foods, Inc., is expanding its Jan. 17 recall of 2.46 oz packages of Shirakiku brand Curvee Puffs Corn Puff Snack curry flavor. The expansion now includes two additional flavors; sea salt and umami flavor and corn potage flavor, because they may contain undeclared milk, according to a Department of Defense All Food and Drug Activity message sent Jan. 29.

The Quaker Oats Company issued a recall of a limited number of two-pound boxes of Pearl Milling Company Original Pancake and Waffle Mix, because they may contain undeclared milk, according to a Department of Defense All Food and Drug Activity message sent Jan. 15.

The Department of Defense (DoD) initiated a recall of Dave's Killer Bread Amped-up protein bars due to the product containing hemp as the first ingredient, according to a DoD All Food and Drug Activity message sent Jan. 13.

Alcon Laboratories is voluntarily recalling one lot of Systane Lubricant Eye Drops Ultra PF, Single Vials On-the-Go, 25 count, due to the potential presence of foreign material which was determined to be fungal in nature, according to a Department of Defense All Food and Drug Activity message sent Jan. 7.

Frito-Lay issued a recall of a limited number of 13-ounce bags of Lay’s Classic potato chips, because they may contain undeclared milk, according to a Department of Defense All Food and Drug Activity message sent Dec. 18.

Russ Davis Wholesale of Wadena, Minnesota, is recalling multiple products out of an abundance of caution because they contain recalled cucumbers from Baloian Farms which may be contaminated with Salmonella, according to a Department of Defense All Food and Drug Activity message sent Dec. 6.

SunFed Produce, LLC (SunFed) is recalling all sizes of whole fresh American cucumbers because they may be contaminated with Salmonella, according to a DeCA internal recall notice from the Defense Commissary Agency’s food safety office sent Nov. 27.

Sugar Foods is voluntarily recalling Fresh Gourmet Santa Fe style tortilla strips, because they may contain wheat, an undeclared allergen, according to an internal recall notice sent Nov. 21.

Grimmway Farms has issued a recall of select organic whole carrots and organic baby carrots due to a possible contamination with Shiga toxin, producing Escherichia coli (E. Coli) O121:H19, according to an internal recall notice sent Nov. 16.