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B. Braun Medical Inc. is recalling three lots of 0.9% Sodium Chloride Injection (saline solution) used in hospitals and healthcare settings. The recalled product contains particles of zinc oxide that should not be present. Intravenous fluids contaminated with particulate matter can cause serious complications including blood clots and organ damage. No injuries have been reported so far.

Serious·FDA·Aug 27, 2026

Lipofit Extreme Fat Burner 2.0 (Lot 25M12F, expiration 09/2027) contains undeclared fluoxetine, a prescription antidepressant, in the daytime tablets and undeclared 2,4-dinitrophenol (DNP), a toxic pesticide, in the nighttime tablets. Neither ingredient is approved for use in dietary supplements, and DNP is not approved by the FDA for any use in humans.

Serious·FDA·Aug 27, 2026·Lipofit

Revival Animal Health recalled Breeder's Edge® and Shelter's Choice® Feline Milk Replacers because some batches contain low levels of potassium, copper, folic acid, choline, and/or vitamin B6. Young kittens depend entirely on milk replacer for nutrition, and these deficiencies can cause anemia, organ damage, and developmental problems within days or weeks.

Serious·FDA·Aug 26, 2026

Seven loaner MiniMed 670G insulin pumps were cleaned with chemically incompatible products that may have damaged the pump casing or keypad. This damage could allow moisture inside the pump and cause it to deliver incorrect insulin doses — either too much or too little — which can lead to serious blood sugar swings.

Serious·FDA·Aug 26, 20263 products

BMC Medical Co., Ltd. is reporting retroactive rework that was conducted on Luna G3 APAP devices at the 3B/React Health warehouse in 2024. This retroactive reporting involves approximately 20,160 units with specific serial numbers.

Serious·FDA·Aug 26, 2026·BMC Medical

Boston Scientific's ENROUTE Transcarotid Neuroprotection System Plus (a catheter used in certain vascular procedures) may experience separation or partial separation of the arterial sheath tip during use. The FDA has classified this as a Class I recall, the most serious type. Approximately 49,229 units with specific lot numbers are affected and were distributed worldwide.

Serious·FDA·Aug 26, 2026

Siemens is recalling two quinidine assay kits, the Syva EMIT 2000 and the Beckman Coulter Emit 2000, because certain lots may give falsely high quinidine measurements. Quinidine is a heart and antimalarial drug, so inaccurate results could lead to inappropriate treatment. The recall covers 75 units total and was distributed in California and Italy.

Serious·FDA·Aug 26, 20262 products

Certain lots of the Siemens Immulite 2000 Syphilis Screen diagnostic assay may incorrectly report low-level positive results as negative. This means some patients with syphilis could receive a false negative result, delaying diagnosis and treatment.

Serious·FDA·Aug 26, 20262 products

BD Needle Kits used for emergency intraosseous (IO) access may have an obturator (the needle's internal plunger) that locks to the needle hub and becomes difficult or impossible to remove after placement. This locking is caused by out-of-tolerance manufacturing dimensions. If the obturator cannot be removed, a new needle may need to be placed, potentially delaying treatment.

Serious·FDA·Aug 26, 2026

Get Fresh Produce Jalapeno Peppers in 2 lb. and 10 lb. boxes may be contaminated with Salmonella. The affected products were distributed in Illinois, Indiana, Michigan, and Wisconsin. No illnesses have been reported to date.

Serious·FDA·Aug 26, 2026

Dairyland Produce, LLC is recalling jalapeno peppers packaged in 5 lb. clear plastic bags due to potential Salmonella contamination. The affected peppers were distributed in Louisiana and Texas. Consumers who have purchased this product should not use it.

Serious·FDA·Aug 26, 2026

Whole Foods Market is recalling 10 refrigerated guacamole dips, salsas and a trio dip sold in its stores because the jalapeños used to make them may be contaminated with Salmonella. The products were sold in clear plastic containers in AR, IA, IL, IN, KY, LA, MI, MN, MO, OH, OK, TX and WI. No illnesses have been reported.

Serious·FDA·Aug 26, 202610 products

Lidl US is recalling Vitasia Asian Style Wok Spice Mix after a positive test for Salmonella bacteria. The affected product is the 1.58 oz (45g) package with lot number 155846 and best-if-used-by date of June 2028. This spice mix was sold in Washington DC, Delaware, Georgia, Maryland, North Carolina, New Jersey, New York, Pennsylvania, South Carolina, and Virginia.

Serious·FDA·Aug 26, 2026

Coast Citrus Distributors is recalling bulk jalapeno peppers packaged between July 1–31, 2026, due to potential Salmonella Javiana contamination. The peppers were distributed in bulk containers to wholesale distributors across the central and eastern United States, with further nationwide distribution for food processing. No retail packages or consumer illnesses have been identified.

Serious·FDA·Aug 26, 2026

Publix is recalling four sizes of its store-brand organic frozen berries, including whole blueberries and whole mixed berries in 10 oz and 48 oz bags, because they may be contaminated with E. coli O145:H28. The products were sold in Alabama, Florida, Georgia, Kentucky, North Carolina, South Carolina, Tennessee, and Virginia, and no illnesses have been reported.

Serious·FDA·Aug 26, 20264 products

American Regent's Papaverine HCl Injection (60 mg/2 mL) has been found to contain particulate matter identified as glass and/or paraformaldehyde. The contamination affects one lot (25202, expiring 11/30/2026) distributed nationwide. This is a prescription injectable medication used to treat certain circulatory conditions.

Serious·FDA·Aug 26, 202612 products

Some Fresenius Kabi morphine sulfate prefilled syringes are labeled as morphine 2 mg/mL but actually contain Dilaudid (hydromorphone) 0.5 mg/0.5 mL. This labeling error could lead to patients receiving the wrong medication and dose. The affected lot is 6402820 with an expiration date of 12/2028.

Serious·FDA·Aug 26, 2026

Bell Sports is recalling certain Pit Boss motorcycle helmets, size medium, manufactured between January 1 and January 31, 2026. These helmets may lack proper impact protection and do not meet federal safety standards, which increases the risk of head injury in a crash.

Serious·NHTSA·Aug 26, 2026·Bell Sports, Inc.

Shanghai Ravioli Corporation recalled approximately 24,900 pounds of frozen Buffalo chicken ravioli and mozzarella sticks produced without federal inspection. The products, sold to foodservice locations in the Northeast, were marked with a false inspection number and may contain undeclared allergens, harmful bacteria, or other contaminants.

Serious·USDA·Aug 26, 2026·Benedetto's

Jaime's Foods ATX recalled Jaime's Spanish Village Jalapeno Ranch dressing because it contains eggs that were not listed on the label or allergen warning. The omission was discovered during an FDA inspection. People with egg allergies or sensitivities could have a serious or life-threatening allergic reaction if they consume this product.

Serious·FDA·Aug 25, 2026

The Better Bakehouse Snack Company recalled certain lots of Donutful Chocolate Dipped Vanilla Cake Donuts because they may contain milk that is not listed on the label. People with a milk allergy or severe sensitivity could have a serious allergic reaction if they eat this product.

Serious·FDA·Aug 25, 2026

Baxter is recalling two lots of 0.9% Sodium Chloride Injection (saline solution) used in hospitals and dialysis centers because fiberglass particles have been found in the solution. The affected lots were distributed to hospitals and medical suppliers in 14 states between July 31 and August 3, 2026. No injuries have been reported so far.

Serious·FDA·Aug 25, 2026

Baxter is recalling one lot of 70% Dextrose Injection used in hospitals and care facilities because stainless steel particles were found in the solution. If given intravenously, these particles could cause blood clots, block blood vessels, or damage organs. No patient injuries have been reported so far.

Serious·FDA·Aug 25, 2026

Certain 2026 Ford Maverick, F-150, and Bronco Sport vehicles have improperly tightened joints that may come loose. This can cause parts to detach, electrical failures, loss of vehicle control, or fire.

Serious·NHTSA·Aug 25, 2026

Certain 2026 Ford Explorer, Bronco, Bronco Sport, Mustang, and Ranger vehicles have engine pistons that may have been manufactured incorrectly. This defect can cause the pistons to fail, resulting in a sudden loss of engine power while driving, which increases the risk of a crash.

Serious·NHTSA·Aug 25, 2026

Certain 2024–2026 Ford Mustang vehicles have wiring harness ground connections in the engine compartment that may fracture. This can cause loss of engine power, headlights, windshield washers, air conditioning, or cooling fan function. Loss of power or headlights increases crash risk.

Serious·NHTSA·Aug 25, 2026

Rennline's lower control arm (part number S180) may have been made with incorrect dimensions, which can damage the vehicle's subframe. A damaged subframe can cause loss of steering control and increase crash risk.

Serious·NHTSA·Aug 24, 2026·Rennline Automotive

Fromm Family Foods is recalling two wet dog food products: Turkey Pâté and Diner Classics Milo's Meatloaf Pâté, sold in 12.2 oz. and 12.5 oz. cans with a Best By date of 032029. The recall is due to potential metal contamination discovered during production. If dogs eat metal, they can choke, vomit, lose appetite, or suffer cuts and blockages in the mouth or digestive tract.

Serious·FDA·Aug 21, 2026·Fromm

Certain 2025–2026 Kia EV9 vehicles have a wiring problem in the Occupant Detection System that may prevent the front passenger air bag from turning off when a child or child seat is present. If the air bag deploys in a crash, a child in the front seat could be seriously injured.

Serious·NHTSA·Aug 21, 2026·Kia America, Inc.

Certain 2027 Peterbilt 567, 579, and 589 trucks and Kenworth T680, T880, and W990 trucks may have a seat ventilation harness missing heat-shrink insulation. This can cause an electrical short circuit that increases the risk of fire.

Serious·NHTSA·Aug 21, 2026