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Certain Chrysler MOPAR roof rack kits have pivot bolts that may not have been tightened properly during manufacturing. The roof rack crossbars can detach while driving, creating a hazard on the road.

Moderate·NHTSA·Sep 10, 2026

ZMC Group's light-up toys—including foam sticks, headbands, jelly rings, and balloon flowers—contain button cell batteries that children can easily access and swallow. Swallowing these batteries can cause serious internal chemical burns and death.

Serious·CPSC·Sep 10, 2026

These six-drawer wood dressers can tip over and trap children if not anchored to the wall. The dressers do not meet federal safety standards required for furniture that children could access.

Serious·CPSC·Sep 10, 2026

The engine rocker arm on certain 2025 and 2026 Triumph TF450 competition motorcycles can seize or stick, causing the exhaust valves to remain open or break. This can lead to sudden loss of engine performance and increased risk of a crash. Triumph has received 12 reports of this problem, including one injury.

Serious·CPSC·Sep 10, 2026·Triumph

These finger light toys contain button cell batteries that children can easily access and swallow. Swallowed button batteries can cause serious internal injuries, chemical burns, and death.

Serious·CPSC·Sep 10, 2026

Certain dual fuel ranges manufactured between March 2025 and July 2026 may be missing a cap on the gas test port. This missing cap can allow gas to leak, creating a risk of fire or explosion. No injuries have been reported so far.

Serious·CPSC·Sep 10, 2026

Prepared Hero fire spray canisters can deteriorate over time and rupture, potentially failing to work during a fire. The company has received nine reports of canisters exploding or deteriorating while in storage. The affected canisters are marked with date code "09/2024" on the base.

Serious·CPSC·Sep 10, 2026

These hair dryer brushes lack a safety device that prevents electrocution if they fall into water while plugged in. They can also overheat and cause burns. One unit was reported to overheat and melt.

Serious·CPSC·Sep 10, 2026

The zipper on Lontcs Busy Board toys contains lead levels that exceed the federal lead paint safety standard. Lead is toxic if swallowed by young children and can cause serious health problems. The toys were sold online through Amazon from May 2024 to July 2026.

Serious·CPSC·Sep 10, 2026

Sweet Cubby children's loungewear sets do not meet federal flammability standards for sleepwear. The two-piece sets (short-sleeved shirt and shorts) sold online can catch fire more easily than safe sleepwear, posing a risk of serious burn injury. About 12,461 sets were sold through SHEIN.com between June 2025 and May 2026.

Serious·CPSC·Sep 10, 2026

Junkins hair dryer brushes (model XR-8801) lack safety features that prevent electrocution if the device falls into water while plugged in. The product also poses a fire risk; there have been 10 reports of smoking or fire, though no injuries yet.

Serious·CPSC·Sep 10, 2026

Victgoal-branded bicycle helmets do not meet mandatory safety standards for retention, stability, and certification. The helmets may fail to protect a rider's head in a crash, creating a serious risk of injury or death. Only red size-small helmets manufactured in November 2025 are affected.

Serious·CPSC·Sep 10, 2026

The rolling ball on Ricky Joy Sour Crush candy bottles can detach and become a choking hazard. These small plastic bottles with liquid sour candy were sold individually and in multi-packs in blue, red, green, and pink flavors at major retailers and online from January 2023 through May 2026.

Serious·CPSC·Sep 10, 2026

Cardinal Health is recalling 12 procedure kits that include BD Urinary Catheter Trays with CliniClean Pericare Wipes. The wipes may be contaminated with a lubricant used during manufacturing. If a contaminated wipe is used on a patient, it may cause localized skin irritation, redness, or mild inflammation. No injuries have been reported.

Moderate·FDA·Sep 9, 202612 products

Fresenius Medical Care is recalling three dialysis acid concentrate products, GRANUFLO, NaturaLyte and Citrasate, after complaints of blue-green discoloration in the product. No injuries have been reported. The products were distributed nationwide in the US and in Mexico.

Moderate·FDA·Sep 9, 20263 products

Specific lots of B Braun's Discofix Four Way Stopcock extension sets have an incorrect expiration date printed on the carton shipper label. This labeling error could affect proper product tracking and usage verification.

Moderate·FDA·Sep 9, 2026

A software issue in the robotic controller of the Medos Velys Enabling Tech Robotic-Assist Station may cause the robotic arm to move unexpectedly during bone preparation or instrument positioning in orthopedic surgery. This affects 29 devices nationwide.

Moderate·FDA·Sep 9, 2026·Medos

Fresenius Medical Care is recalling four 5008X blood tubing set models because the connection between the Arterial Alpha Clip and the main line or pump segment may leak blood during treatment. A leak could cause blood loss and low blood volume. No injuries have been reported.

Moderate·FDA·Sep 9, 20264 products

Boston Scientific is recalling server software that supports its LUX-Dx, LUX-Dx II, and LUX-Dx II+ insertable cardiac monitors. The recall covers three products, one for each region: US, EU, and ANZ. The software can delay notifications of AF Burden Alerts, which are alerts about atrial fibrillation, and a delayed alert may delay clinical review or treatment. No injuries have been reported.

Moderate·FDA·Sep 9, 20263 products

Medline is recalling 13 convenience kits that contain BD ChloraPrep Clear 1mL applicators from specific lots. The applicator packaging may have an open or incomplete seal, so the applicator could be contaminated. Contaminated applicators can cause skin or soft tissue infections, or more serious infections, and no injuries have been reported.

Moderate·FDA·Sep 9, 202613 products

Baxter is recalling two Novum IQ syringe pump models, totaling about 14,605 units. During a Volume/Time (VOT) multi-syringe infusion, a software issue may occur if a syringe runs empty and is replaced while the Volume To Be Infused (VTBI) is still remaining. No injuries have been reported.

Moderate·FDA·Sep 9, 20262 products

Johnson & Johnson is sending updated surgical instructions for HEALON EndoCoat PRO and HEALON DUET PRO II viscoelastic products used in cataract surgery. The new instructions emphasize that if resistance is felt when inserting the cannula, surgeons should stop, withdraw the cannula, and reassess insertion conditions rather than forcing it—to avoid potential injury to the cornea, iris, or Descemet's membrane (a delicate eye structure).

Moderate·FDA·Sep 9, 2026·Johnson & Johnson Surgical Vision

Medline is recalling 16 convenience kit products that contain BD ChloraPrep Clear or FREPP Clear antiseptic applicators. Wrinkles in the paper lidding may extend to the seal, which could break the sterile packaging and allow microbial contamination. No injuries have been reported.

Moderate·FDA·Sep 9, 202616 products

Diagnostica Stago identified a positive drift in quality control (QC) values in one lot of STA Staclot Protein S reagent within the product's stated 4-hour stability period. This drift could affect the accuracy of test results performed during that window. The issue affects reagent Lot 273074 distributed nationwide.

Moderate·FDA·Sep 9, 2026

Medicom is recalling specific lots of Ritmed Neurological Sponges (non-sterile models 55992C to 55998C) because their endotoxin levels may vary unexpectedly. AVID Medical is recalling three groups of Halyard medical convenience kits that contain these sponges, about 28,800 kits in total. No injuries have been reported.

Moderate·FDA·Sep 9, 20263 products

Philips is recalling four CT scanner product lines, covering 4 product groups, because an unintended radiation issue could affect how the equipment performs. The recall covers Philips Brilliance, IQon Spectral CT, Ingenuity CT, and Brilliance CT 64 systems distributed in the US and US territories. No injuries have been reported.

Moderate·FDA·Sep 9, 20264 products

Fayus Inc. recalled OLA-OLA Pounded Yam (Iyan) products in 2 lb, 4 lb, 5 lb, and 10 lb bags because some packages contain undeclared milk. The product was mislabeled during packaging for different markets. This poses a serious risk to people with milk allergies or sensitivities.

Serious·FDA·Sep 9, 2026

Frankie's Organic Plant-Based Puffs Vegan Cheddar (4 oz bags) tested positive for milk, which is not listed on the package label. This poses a serious risk to people with milk allergies or those avoiding dairy. The affected product was distributed to retailers in Washington, Florida, South Carolina, and select independent stores.

Serious·FDA·Sep 9, 2026

Ukrop's Homestyle Foods is recalling two sizes of Ukrop's Bread Pudding with Vanilla Sauce, a 13.8 oz single-serve product and a 4 lb kit, because they may contain small metal fragments. The products were shipped to stores in Kentucky, North Carolina, Virginia and West Virginia. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Ukrop's2 products

Wonton Specialist Inc. is recalling six products sold as pan fried noodles, wonton noodles, lo mein noodles, cooked noodles, wonton skins and dumpling skins. The products contain FD&C Red No. 40, a synthetic food dye, but the dye is not listed on the label. The products were distributed in New York, New Jersey and Pennsylvania, and no injuries have been reported.

FDA·Sep 9, 20266 products