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Lee K of NY Issue Allergy Alert on Undeclared Allergen (Milk and Shrimp) in “Stewed Aged Kimchi w/Mackerel”

Lee K of NY INC of Flushing, NY, is recalling it’s 57-ounce packages of “Stewed Aged Kimchi w/ Mackerel” in…

Middlefield Original Cheese Co-Op Recalls Organic Gouda, Colored Cheddar, Mozzarella/Provolone, Pepper Jack, Swiss, Dilly Pickle Cheese and Monterey Jack Due to Possible Listeria Monocytogenes Contamination

Middlefield, OH 9/5/25 – The Middlefield Original Cheese Co-Op facility in Middlefield, OH is recalling one lot of Sunrise Creamery…

Tobacco Products

Tobacco comes in many forms, from cigars and cigarettes to smokeless tobacco and dissolvable nicotine products. FDA works to reduce…

Properly Store Nicotine Pouches to Prevent Accidental Exposure to Children and Pets

Nicotine pouches can be dangerous to children if they use, touch, chew on, or eat them. These small fiber pouches,…

Updated Release: Southwind Foods, LLC Recalls Frozen Shrimp Because of Possible Health Risk

Southwind Foods, LLC of Carson, California is voluntarily recalling a limited quantity of Frozen Shrimp, due to possible radionuclide (Cesium-137)…

Hans Kissle LLC Issues Allergy Alert on Undeclared Wheat (Allergen) in Hans Kissle Red Potato Bliss Salad

Haverhill, MA — Hans Kissle is voluntarily recalling 120 units of Hans Kissle Red Potato Bliss Salad due to undeclared…

Mobile Power Unit AC Power Cord Recall: Abbott Medical Removes AC Power Cord Associated with HeartMate Mobile Power Unit (MPU) Due to Potential Risk of the Cord Not Locking into Place

Abbott Medical is removing power cords associated with the HeartMate Mobile Power Unit due to a potential risk of the…

Breathing Circuit Set Recall: Hamilton Medical, Inc. Removes Coaxial Breathing Circuit Set Due to Possible Inner Blue Tube Cracks That May Impact Ventilation

Hamilton Medical is recalling certain coaxial breathing sets due to a defect that may cause cracks in the inner tube,…

Green Lumber Holding, LLC Issues Consumer Alert on Counterfeit Products Following FDA Findings

Costa Mesa, California August 28, 2025 – Green Lumber Holding, LLC (“Green Lumber”) is alerting consumers that counterfeit products misrepresented…

Manual Resuscitator Recall: Ambu Inc. Removes SPUR II Resuscitators Due to Blocked Manometer Port

A blocked manometer port on the Ambu SPUR II resuscitator may delay ventilation or cause barotrauma