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FDA
September 8, 2025
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…
FDA
September 5, 2025
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…
FDA
September 2, 2025
Tobacco Products
Tobacco comes in many forms, from cigars and cigarettes to smokeless tobacco and dissolvable nicotine products. FDA works to reduce…
FDA
September 2, 2025
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,…
FDA
August 29, 2025
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)…
FDA
August 29, 2025
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…
FDA
August 28, 2025
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…
FDA
August 28, 2025
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,…
FDA
August 28, 2025
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…
FDA
August 28, 2025
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
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