Cosmetic Recalls
Henkel Corp recalls Schwarzkopf Professional Extra Strong Mousse
Rocky Hill, CT -- Henkel Corporation (“Henkel”) is voluntarily recalling its Schwarzkopf Professional Osis Grip 6.76 fl. Oz/200 ml sold in the United States due to a potential packaging issue in which product could leak from the package under pressure, which creates a risk of explosion.
The Schwarzkopf Professional Osis Group 6.76 Oz/200ml comes in aluminum cans in 25 Lots with Batch Codes listed in article links above.
Drug and Medical Device Recalls
Fresenius Kabi recalls Fresenius Kabi Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL
FOR IMMEDIATE RELEASE – 8/4/2026 – LAKE ZURICH, Ill.— Fresenius Kabi, an operating company of the Fresenius Group, is voluntarily recalling one lot of Morphine Sulfate Injection USP, Simplist® 2 mg/1 mL due to a label mix-up. The MicroVault labeled as Morphine 2 mg/1 mL, may contain a Prefilled Syringe of Dilaudid 0.5 mg/0.5 mL. This recall is being conducted to the user level.
Use of a MicroVault labeled as Morphine Sulfate Injection 2 mg/mL containing a prefilled syringe of Dilaudid (hydromorphone HCl) 0.5 mg/0.5 mL has a reasonable probability of causing serious adverse health consequences, including life-threatening respiratory depression and death. Patients at greatest risk include individuals who do not use opioids on a regular basis, those with underlying respiratory disease, pediatric patients, and those who are also taking central nervous system (CNS) depressants. To date, no adverse event reports have been received for this lot number.
Fresenius Kabi recalls Fresenius Kabi Tyenne Injection 400 mg/20 mL vial
August 10, 2026 – LAKE ZURICH, Ill.— Fresenius Kabi, an operating company of the Fresenius Group, is recalling one lot of Tyenne® (tocilizumab-aazg) Injection 400 mg/20 mL (20 mg/mL)20 mL vials to the user level. An internal investigation at the firm found the product to contain glass particles.
Risk Statement:The administration of an injectable product containing glass particulates may cause local irritation, pain, or swelling at the infusion site, as well as inflammation of the veins. More seriously, glass particles can cause blockage and clotting in blood vessels, which can cut off blood flow to vital organs, lead to a life-threatening blood clot in the lungs (pulmonary embolism) and cause permanent organ damage or death.
Tyenne® (tocilizumab-aazg) Injection is indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis who have had an inadequate response to one or more disease-modifying antirheumatic drugs (DMARDs); adult patients with giant cell arteritis; patients 2 years of age and older with active polyarticular juvenile idiopathic arthritis; patients 2 years of age and older with active systemic juvenile idiopathic arthritis; adults and pediatric patients 2 years of age and older with chimeric antigen receptor (CAR) T cell-induced severe or life-threatening cytokine release syndrome; and certain hospitalized adult patients with COVID-19.
Medline Industries, LP recalls Medline, Teleflex Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits
On July 13, 2026, Medline Industries, LP initiated a nationwide recall of Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits. Medline received reports of sporadic failures involving the electrical connector of certain neonatal and infant heated wire breathing circuits. In affected circuits, the heated wire connector (pigtail) at the Neptune humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage. To date, reported events have occurred infrequently relative to the number of devices distributed, with the observed occurrence rate of 0.011% across the distributed population. Refer to the below photographs of the product and a defect that was reported to Medline.
The Neptune humidifier is designed with safety features that continually monitor the heated wire circuit and automatically discontinues power to the heated wires when electrical abnormalities are detected. When power to the heated wires is disconnected, respiratory gas flow to the patient continues. The disconnection of power is limited to the heated wire function.
Victory Medical Center Pharmacy recalls VMC Compounded Glutathione 200 mg/mL Multi-Dose Vials
FOR IMMEDIATE RELEASE – August 5, 2026 – Austin, Texas, Victory Medical Center Pharmacy is voluntarily recalling certain lots of Compounded Glutathione 200 mg/mL Multi-Dose Vials to the patient level. The product is being recalled because pharmacy testing identified elevated bacterial endotoxin levels
Risk Statement: There is reasonable probability that injectable products with elevated endotoxin levels could cause significant medical events including fevers, hypotension, inflammatory reactions, anaphylactic shock and death. To date, Victory Medical Center Pharmacy has received reports of adverse events including fever, chills, severe headache, nausea, vomiting, tachycardia, changes in blood pressure, body aches, and instances of injection site reactions.
Food and Beverage Recalls
Blank Slate Creamery recalls Blank Slate Creamery Vegan Non-Dairy Frozen Dessert Coconut Fudge Sandwiches
Blank Slate Creamery of Ann Arbor, MI is recalling its 4.5 oz. packaged VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, because it may contain undeclared egg. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
The VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICH was distributed in Ann Arbor and Brighton, MI at 3 store locations.
The product comes in a 4.5 ounce, clear plastic package marked with a best by dates 11/23/26 and 1/9/27.
No illnesses have been reported to date in connection with this issue.
Lexunder Inc. dba Food To Live recalls Food To Live Green Powder Products
Lexunder Inc Recalls Food to Live Brand Green Powder Products Because of Possible Health Risk
Lexunder Inc., doing business as Food To Live of Brooklyn, NY, is recalling Food to Live brand green powder products because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis, and arthritis.
The products were sold nationwide. They were sold online to consumers and businesses through foodtolive.com, foodinbulk.com, and other online marketplaces.
The recalled Food to Live branded products were sold in resealable stand-up pouches and bulk cases, weighing 33, 44, and 55 pounds.
Sun Noodle of Honolulu recalls Sun Noodle Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base
August 5, 2026 — Sun Noodle of Honolulu, Hawaii is voluntarily recalling 134 packages (15.4oz) of Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base, because the product may contain undeclared fish allergen. People who have an allergy or severe sensitivity to fish run the risk of a serious or life-threatening allergic reaction if they consume this product.
The recalled Sura Tanmen, lot #1226183, was distributed exclusively in the state of Hawaii through the following retail supermarkets and food distributors between July 9 and July 29, 2026, a list in the article linked above.
Taylor Fresh Foods recalls Trader Joe’s, Freshness Guaranteed and more Finished products (e.g. dips, salsa, guacamole and more) containing jalapeno
Taylor Fresh Foods Recalls Products Made with Jalapeno Peppers Because of Possible Health Risk
Salinas, Calif., August 9, 2026 – Upon notification that Coast Citrus Distributors is voluntarily recalling fresh jalapeños due to potential Salmonella contamination, Taylor Fresh Foods is recalling finished products containing jalapeños subject to this recall.
Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections, endocarditis, and arthritis.
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