Colorado recalls

Sold nationwide. 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·Wantefully

Sold nationwide. 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·SQT

Sold nationwide. 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·Sweet Cubby

Sold nationwide. 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·Junkins

Sold nationwide. 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·Keben

Sold nationwide. 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·Ricky Joy

Sold nationwide. 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, 2026·Cardinal Health12 products

Sold nationwide. 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, 2026·Fresenius Medical Care3 products

Sold nationwide. 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·B. Braun

Sold nationwide. 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

Sold nationwide. 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, 2026·Fresenius Medical Care4 products

Sold nationwide. 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, 2026·Boston Scientific3 products

Sold nationwide. 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, 2026·Medline13 products

Sold nationwide. 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, 2026·Baxter2 products

Sold nationwide. 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

Sold nationwide. 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, 2026·Medline16 products

Sold nationwide. 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·Diagnostica Stago

Sold nationwide. 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, 2026·AVID Medical3 products

Sold nationwide. 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, 2026·Philips4 products

Sold nationwide. Savor Seasonings LLC's bulk Organic Cheddar Type Seasoning tested positive for milk allergen that was not listed on the label. The affected product is packaged in 50-lb bags and distributed in Canada. This poses a serious risk to people with milk allergies.

Serious·FDA·Sep 9, 2026·Savor Seasonings

Sold nationwide. The Hampton Grocer's Lacnola Small Batch Lactation Granola (8 oz pouches) may be contaminated with Salmonella. Two specific lot codes are affected: HGLC-102125 (expires 21 Oct 2026) and HGLC-021326 (expires 13 Feb 2027).

Serious·FDA·Sep 9, 2026·The Hampton Grocer

Sold nationwide. Optimal Balance Pharmacy's Glutathione 200 mg/mL injectable solution failed quality testing and was found to contain bacterial endotoxin levels above safe limits. This contamination poses a risk of serious infection or systemic reaction when injected. The affected lot (LG342009076) was distributed nationwide.

Serious·FDA·Sep 9, 2026·Optimal Balance Pharmacy

Sold nationwide. Baxter Healthcare Corporation is recalling 0.9% Sodium Chloride Injection USP in 500 mL VIAFLEX plastic containers because some bags contain fiberglass particles. The affected lots are Y495523 and Y495523A, expiring October 31, 2027. No injuries have been reported.

Serious·FDA·Sep 9, 2026·Baxter

Sold nationwide. American Health Packaging distributed buprenorphine sublingual tablets with incorrect labeling. The affected medication is a prescription opioid used to treat pain and opioid use disorder. A label mix-up could result in dosing errors if patients or healthcare providers rely on incorrect information.

Moderate·FDA·Sep 9, 2026·American Health Packaging

Sold nationwide. Mylan Pharmaceuticals is recalling Prasugrel 10mg tablets (Lot #3225272, expiring September 30, 2026) because they failed dissolution testing during 18-month stability studies. This means the tablets may not break down and release the medication as intended in the body. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Mylan

Sold nationwide. Sage Products is recalling specific lots of 2% Chlorhexidine Gluconate non-sterile cloths due to potential cross-contamination with other products during manufacturing. The affected cloths may not meet safety and quality standards. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Sage Products

Sold nationwide. Teva Pharmaceuticals discovered that some bottles of trazodone 50 mg tablets contain foreign tablets or capsules mixed in with the correct medication. The issue affects one lot (1394026) with an expiration date of February 2028. No injuries have been reported.

Moderate·FDA·Sep 9, 2026·Teva

Sold nationwide. Supernus Pharmaceuticals is recalling one lot of Trokendi XR (topiramate) 50 mg extended-release capsules because the medication did not dissolve as designed. When a medication fails to dissolve properly, the body may not absorb the full dose, potentially reducing its effectiveness.

Moderate·FDA·Sep 9, 2026·Supernus

Sold nationwide. Mylan Pharmaceuticals is recalling specific lots of Mycophenolate Mofetil for injection (500 mg/vial) because the medication failed to meet dissolution specifications—meaning the drug may not dissolve properly in the body. This could affect how well the medicine works. The recall affects two lots distributed nationwide.

Moderate·FDA·Sep 9, 2026·Mylan

The FDA recall covers two Broadway Joe's pain creams containing CBD and hempseed oil, sold in 2 oz and 4 oz jars. The recall was made because of possible contamination of a raw material, found through manufacturing quality issues. The products were distributed in Colorado, and no injuries have been reported.

Moderate·FDA·Sep 9, 2026·Lexia2 products