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These wooden dressers can tip over and trap children if not securely anchored to the wall. The dressers do not meet federal safety standards for clothing storage furniture. No injuries have been reported.

Serious·CPSC·Sep 3, 2026

GE is recalling four Portrait Core Services software products because a software issue may cause a loss of patient monitoring at the Hub and Central Viewer. After the update, alarm settings may also reset to factory defaults and no longer match the settings configured for each patient or care area. No injuries have been reported.

Serious·FDA·Sep 2, 20264 products

IMRIS is recalling 2 operating room table models, the ORT200 and ORT300, with 19 affected units. A mechanical failure in the linear actuator and rotational lock can stop the table from switching between locked and unlocked, which could allow unintended rotation during a procedure. No injuries have been reported.

Serious·FDA·Sep 2, 2026·IMRIS2 products

Medline is recalling three neonatal and infant heated wire breathing circuit products, about 417,000 units in total. The heated wire connector at the humidifier can fail and show discoloration, melting, smoke, or a burning odor. Failure could cause breathing problems in infants, and no injuries have been reported.

Serious·FDA·Sep 2, 20263 products

Jaime's Foods ATX Jalapeno Ranch dressing in 16 oz. glass jars may contain egg, which is not declared on the label. People with egg allergies could have a serious reaction if they consume this product. The recall affects 102 cases distributed in Texas.

Serious·FDA·Sep 2, 2026

bettergoods brand Pistachio Nut Butter (6.7 oz jars) may be contaminated with Salmonella. The affected product has lot number LB028ACP04 with an expiration date of January 28, 2027, and was distributed across 19 states.

Serious·FDA·Sep 2, 2026

Dreyer's is recalling six Outshine fruit bar products because they may contain pieces of glass. The recall covers Strawberry, Watermelon, Grape, Tangerine and Black Cherry 6-count packs, plus a 24-count variety pack of Strawberry, Pineapple, Grape and Tangerine bars. No injuries have been reported.

Serious·FDA·Sep 2, 2026·Outshine6 products

ZMB Enterprises' Addall XR Shot 1 liquid dietary supplement contains three undeclared ingredients that are banned or restricted by the FDA: 1,4-DMAA, Phenylethylamine, and Phenibut. The product was sold online between July and December 2025.

Serious·FDA·Sep 2, 2026

Sirna & Sons Produce has recalled 1-pound bags of jalapeño peppers that may be contaminated with Salmonella Javiana. The affected product was packed on July 13 or July 23, 2026, and distributed to food service locations in Ohio and Pennsylvania.

Serious·FDA·Sep 2, 2026

Khong Guan is recalling two sizes of its glutinous rice balls with black sesame filling, 14.1 oz (400 g) each, because they may contain peanuts that are not listed on the label. The recall covers two UPC products, both made in China and sold in AZ, CA, CO, HI, NJ, OR, TX and WA. No illnesses have been reported.

Serious·FDA·Sep 2, 20262 products

Sun Noodle's Sura Tanmen Hot and Sour Flavor ramen noodle kit contains a soba sauce packet with fish (bonito, sardine, and mackerel), but the package label does not disclose these fish allergens. This poses a risk to people with fish allergies. About 140 packages were distributed in Hawaii.

Serious·FDA·Sep 2, 2026·Sura

B. Braun Medical has recalled Lactated Ringer's Injection USP in 1000 mL EXCEL containers due to the presence of particulate matter. The affected lot is J4H077 with an expiration date of November 30, 2026. About 23,688 bags were distributed nationwide.

Serious·FDA·Sep 2, 2026

Fresenius Kabi USA discovered that Tyenne (tocilizumab-aazg) Injection vials may contain glass particles. The contamination was found during an internal investigation. The affected lot is 16UI07, which expires August 31, 2028.

Serious·FDA·Sep 2, 2026

A software error in the battery management system of certain 2026 Toyota C-HR electric vehicles can cause the battery to overcharge under specific driving conditions. This overcharge can shut down the drive system, leaving the vehicle without power and increasing crash risk.

Serious·NHTSA·Sep 2, 2026

Certain 2026–2027 Storyteller Overland MODE and 2026 GXV HILTS vehicles have a printed circuit board in the rooftop ventilation fan that may overheat during use. An overheated circuit board can cause a fire.

Serious·NHTSA·Sep 1, 2026·Storyteller Overland

The furnace exhaust in certain 2027 Forest River Vibe recreational trailers may not be correctly attached to the outside flue. This can allow carbon monoxide to build up inside the trailer cabin, creating a risk of poisoning.

Serious·NHTSA·Sep 1, 2026

Certain 2021–2023 Jeep Grand Cherokee, Grand Cherokee L, and Grand Cherokee 4XE models may have rear coil springs that were incorrectly installed. These springs can detach while the vehicle is driving, which increases the risk of losing control and crashing.

Serious·NHTSA·Sep 1, 2026

A cracked brake pedal position sensor can cause the electronic stability control system to stop working in certain 2025–2026 Chrysler Voyager, Chrysler Pacifica, and 2026 Voyager Plug-In Hybrid vehicles. Without stability control, the risk of losing vehicle control and crashing increases.

Serious·NHTSA·Sep 1, 2026

Certain 2026 Tesla Model Y vehicles have front suspension lateral link fasteners that may not have been properly tightened. If a lateral link loosens or separates, it can shift wheel alignment and cause loss of vehicle control, increasing crash risk.

Serious·NHTSA·Sep 1, 2026·Tesla, Inc.

Crystal Temptations Chocolatey Eyeballs contain milk that is not listed on the label. People with a milk allergy or sensitivity could have a serious allergic reaction if they eat these candies. No illnesses have been reported so far.

Serious·FDA·Aug 31, 2026

Certain 2026–2027 Tiffin Wayfarer motorhomes may have propane tanks that are loose in their mounting brackets and lack a remote shut-off valve. A loose tank could detach while driving and become a road hazard, and a tank without a shut-off valve increases fire risk.

Serious·NHTSA·Aug 31, 2026·Tiffin Motorhomes, Inc.

Northwest Naturals has recalled two frozen raw pet food products because they may be contaminated with Salmonella and/or Listeria monocytogenes. The affected products are the Frozen Chicken Recipe (cat food, 2 lb. bags) and Frozen Raw Diet for Dogs Chicken Recipe (6 lb. bags) in specific lots. No illnesses have been reported so far.

Serious·FDA·Aug 29, 2026

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