Oregon recalls

Sold nationwide. Siemens is recalling four ACUSON ultrasound imaging systems: ACUSON Orgin, ACUSON Orgin ICE, ACUSON Sequoia and ACUSON Sequoia Select. A software issue may cause the Color Doppler setting to activate unintentionally. That setting has not received FDA clearance, and the activation could cause the system to crash or become unresponsive. The recall was distributed in the US states of CA, CT, KY, NC and TX and in Germany, Italy and India.

Moderate·FDA·Nov 6, 2026·Siemens4 products

Sold nationwide. TransMedics is recalling three OCS Liver System products: Liver Perfusion Sets (model 3200), Liver Solution Infusion Sets (model 3457), and Solution Delivery Cassettes (model 1467). The cassettes were assembled with syringes made with an atypical lubricant, which may cause sub-par performance and has the potential to cause leaks. The recall covers 1,179 perfusion sets, 90 infusion sets and 55 cassettes, distributed nationwide in Nebraska and to Italy, and no injuries have been reported.

Moderate·FDA·Nov 6, 2026·TransMedics3 products

Sold nationwide. Medtronic Xomed recalled two ear ventilation tube products, the Sheehy Ventilation Tube 5PK Button 1.27 FLPL and the Bobbin Ventilation Tube 5PK 1.14 FLPL, because the tubes were not subjected to the required sterilization process. After implantation, this could cause infection and inflammation, potentially leading to temporary hearing impairment, ear fluid discharge, and the need for antibiotics. The notice reports no injuries.

Moderate·FDA·Nov 6, 2026·Medtronic Xomed2 products

Sold nationwide. TransMedics recalled three OCS products: the OCS Heart Perfusion Set (Model 1200), the OCS Liver Perfusion Set (Model 3200), and the OCS Heart Instrumentation Tool Set (Model 1401). The FDA says the device kits were incorrectly assembled and include incorrect components. The recall was distributed nationwide in the US (NE, AZ, CA, FL, GA, IL, MA, MI, MN, NC, NJ, OH, TX, UT, WA) and in Australia, France, Italy and Taiwan. No injuries have been reported.

Moderate·FDA·Nov 6, 2026·TransMedics3 products

Sold nationwide. This recall covers 46 TransMedics OCS Liver Perfusion Sets (model 3200), which were incorrectly assembled and contain incorrect accessories. The sets were distributed in 12 states, and no injuries have been reported.

Moderate·FDA·Nov 6, 2026·TransMedics

Sold nationwide. TransMedics is recalling three OCS organ perfusion sets used for organ transport: the OCS Heart Perfusion Set (Model 1200, software rev 3), the OCS Liver Perfusion Set (Model 3200, software rev 3), and the OCS Lung Mission Critical Plus Perfusion Set (Model 2200, software rev 1). The perfusion module in these sets may have an unprogrammed Front End Board, which can stop the system from getting past startup and cause it to show the error "Unsupported Perfusion Module Present." The notice says the product was distributed worldwide, including nationwide in the US in several states and in Serbia, and reports no injuries.

Moderate·FDA·Nov 6, 2026·TransMedics3 products

Sold nationwide. Vesco Medical is recalling 7 Vesco Q products: the Vesco Q Enteral Feeding Pump (model VED-701) and six Vesco Q feed sets (models VED-050, VED-051, VED-052, VED-053, VED-054 and VED-059). The pump may deliver enteral fluids outside its labeled accuracy of plus or minus 5%, so feeds may be over- or under-delivered compared with the prescribed dose. The agency says this could cause temporary or medically reversible effects, with a remote chance of serious harm. No injuries have been reported.

Moderate·FDA·Nov 6, 2026·Vesco Medical7 products

Sold nationwide. Four Siemens ARTIS imaging systems are in this recall: ARTIS icono biplane, ARTIS icono ceiling, ARTIS icono floor and ARTIS pheno. The systems may not carry out movement control commands as intended, and may show the message "Limited stand/table movement, SC." The affected units are in California, Kentucky, New York and Texas, and no injuries have been reported.

Moderate·FDA·Nov 6, 2026·Siemens4 products

Sold nationwide. Some TCD radiofrequency electrodes may have small cut marks on the Tyvek side of the sterile pouch. If the sterile barrier is compromised and the devices are used, microbial or other foreign material could enter patient tissue, which may lead to infection, pain, inflammation, allergic reaction, or the need for more medical or surgical treatment. No injuries have been reported.

Moderate·FDA·Nov 6, 2026·Boston Scientific

Sold nationwide. Philips Medical Systems Nederland B.V. is recalling Allura Xper systems running software releases R8.1.x or R8.2.x that are configured with a FlexVision monitor. The software issue may cause the FlexVision software application to become unresponsive during clinical use.

Moderate·FDA·Nov 6, 2026·Philips

Sold nationwide. Zynex Medical M-Wave muscle stimulators may deliver constant electrical impulses to all four electrodes at once, instead of alternating between them as designed. This may cause muscle fatigue. The recall covers model 701200 with firmware 4.3 and was distributed nationwide. No injuries have been reported.

Moderate·FDA·Nov 6, 2026·Altivera Medical

Sold nationwide. Siemens is recalling two Atellica CH reagents: Atellica CH HDL Cholesterol (HDLC) and Atellica CH Total Protein_2 (TP_2). Reagent probe carryover on the Atellica CH and Atellica CI analyzers may cause falsely elevated Hemoglobin A1c results and falsely depressed Direct Bilirubin 2 results, which may affect patient samples, quality control, and calibrator results. No injuries have been reported, and the products were distributed in the US and many other countries.

Moderate·FDA·Nov 6, 2026·Siemens2 products

Sold nationwide. Medtronic is recalling 3 related products used to program and check Medtronic cardiac implantable devices: the CareLink SmartSync Device Manager App (M01A02), the Programmer 24970A, and the RF Head 24967 Patient Connector and RF Head 24967 EUR MKT. Bluetooth disconnections may occur between the device manager software and its accessories, and during a SmartSync patient session this may lead to undesirable or incomplete parameter programming that could cause harm. No injuries have been reported.

Moderate·FDA·Nov 6, 2026·Medtronic3 products

Sold nationwide. W L Gore & Associates is recalling certain GORE VIABAHN Endoprosthesis devices with Heparin or PROPATEN Bioactive Surface. The devices were made on equipment that was not operating with valid parameters, which may cause the distal tip to separate. The notice reports no injuries.

Moderate·FDA·Nov 6, 2026·Gore

Sold nationwide. USDA's Food Safety and Inspection Service is issuing a public health alert for frozen meat and poultry products that contain sesame, which is not listed on the labels. The beef product also contains Worcestershire sauce with anchovy (fish), which is not declared either. The products were produced Oct. 15, Oct. 16 and Oct. 27, 2026, and the agency has no confirmed reports of reactions.

Moderate·USDA·Nov 6, 2026·Lowlands House

Sold nationwide. ORL Labs is recalling six ORL Organic Oral Care kids' and adult toothpaste and mouthwash products sold nationwide. The FDA's sampling found progesterone, estradiol, or DHEA (a hormone) in the products, which the company says is due to cross-contamination. No injuries have been reported.

Moderate·FDA·Nov 6, 2026·ORL Labs6 products

Sold nationwide. Luminex updated the Instructions for Use for the LIAISON PLEX Gram-Negative Blood Culture Assay to say that repeat testing is recommended whenever a positive family-level-only result is obtained. FDA says the issue may contribute to incorrect or delayed diagnosis of bloodstream infection. No injuries have been reported.

Moderate·FDA·Nov 5, 2026·Luminex

Sold nationwide. The shelf label on a Halyard Arthroscopy Pack was printed as "Extremity" instead of "Arthroscopy Pack." The recall covers 17 kits, and the notice reports no injuries.

Moderate·FDA·Nov 5, 2026·AVID Medical

Sold nationwide. Huvepharma Inc is recalling Sulmet Soluble Powder (sodium sulfamethazine), an antibacterial for animal use only, because the pouches have incorrect expiration dates printed on them. The recall covers lot YSL057, which shows an expiration date of JUL2028, and was distributed nationwide in the U.S. The notice reports no injuries.

FDA·Nov 5, 2026·Sulmet

Sold nationwide. Neogen is recalling two horse powders, UNIPRIM Powder for Horses and Apple Flavored UNIPRIM Powder for Horses, both containing trimethoprim and sulfadiazine in 400-gram containers. The recall is due to a defective container closure. The FDA has classified it as Class II.

Moderate·FDA·Nov 5, 2026·UNIPRIM2 products

WinCo Foods LLC is recalling its 16 oz Hoagie Rolls because they contain sesame, which is not listed on the label. The rolls were sold in CA, ID, MT, NV, OR, UT, and WA, and the FDA has classified this as a Class I recall.

Serious·FDA·Nov 5, 2026·WinCo Foods

Ethel's Bakery, LLC is recalling 6 oz Ethel's Gluten Free Turtle Dandy Dessert Bars because of a product mix-up. The label lists ingredients that are not in the product, and the Nutrition Facts are inaccurate.

FDA·Nov 5, 2026·Ethel's Gluten Free

Sold nationwide. American Regent notified BluePoint Laboratories of potential glass particle contamination in a batch of cyanocobalamin injection, USP, 1,000 mcg/mL, sold in 25-vial cartons. The recall covers lot 24394A, expiration 10-31-2026, with about 4,097 cartons distributed nationwide. No injuries have been reported.

Moderate·FDA·Nov 5, 2026·American Health Packaging

Sold nationwide. Magnets in these magnetic building cubes can become loose if the cubes break or open, posing a magnet ingestion hazard to children. Swallowed magnets can attract each other or metal objects and become lodged in the digestive system, which can cause intestinal perforations, twisting or blockage, blood poisoning, and death. No injuries have been reported.

Serious·CPSC·Nov 5, 2026·Magnetopia

Sold nationwide. The speed-adjusting module included with these youth ATVs can let the vehicle's speed be raised above the maximum for children 6 and older, posing a risk of serious injury or death from a crash. About 117 units were sold online at Walmart.com, Powersportsmax.com, Xprousa.com, Amazon.com and eBay.com from July through September 2025 for between $680 and $980. No injuries have been reported.

Serious·CPSC·Nov 5, 2026·U.S. Titan

Sold nationwide. Sanven Technology Ltd. is recalling about 1,950 Vevor-branded 20-inch and 24-inch BMX bicycles, models SS24001 and SS24002. The bicycles lack a chain guard, so loose clothing can get caught in the chain drive, posing a risk of serious injury or death from a crash. The bicycles also do not meet labeling requirements.

Serious·CPSC·Nov 5, 2026·Sanven Technology

Sold nationwide. Baby Brezza Enterprises is recalling about 29,000 SuperFast Sterilizer Dryers sold in the U.S., plus about 4,500 sold in Canada. The units can overheat when plugged in and operating, which may cause burns if the surface is handled. The firm has received 32 reports of overheating or melting plastic housing, and no injuries have been reported.

Moderate·CPSC·Nov 5, 2026·Baby Brezza

Sold nationwide. Kikea Store is recalling X-VESOLJE nursing pillows, model NP001, because they violate mandatory safety standards for nursing pillows. The pillows can obstruct an infant's breathing, posing a serious risk of injury or death from suffocation. No injuries have been reported.

Serious·CPSC·Nov 5, 2026·Kikea Store

Sold nationwide. A screw on the recalled ice axes can loosen during use, causing the handle or pick to detach. The agency says this poses a risk of serious injury or death from a fall. No injuries have been reported.

Serious·CPSC·Nov 5, 2026·C.A.M.P

Sold nationwide. The oven doors can unexpectedly close when bumped, posing a burn hazard to people retrieving hot food. Gourmia has received 57 reports of doors closing unexpectedly when retrieving food, resulting in 40 incidents of burns to hands or wrists. About 175,951 ovens were sold at Target stores nationwide and on Target.com from October 2021 through June 2026 for about $150.

Moderate·CPSC·Nov 5, 2026·Gourmia