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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.
More categories (17)
- 2026-10-15NHTSAPrevost Car (US) Inc.Prevost buses recalled for missing emergency exit label
Certain Prevost buses are missing the emergency exit operating instruction label on the entrance door. This label is required by federal safety standards and helps passengers evacuate safely in an emergency.
- 2026-10-15NHTSA-EquipmentVolvo Trucks North AmericaVolvo Trucks sleeper cabs recalled for loose structural bolts
Certain Volvo Trucks replacement sleeper cabs (VNL660 and VNL860 models) may have loose or missing structural bolts that attach the cab to the frame. If bolts are not properly secured, the sleeper cab may not protect occupants as intended during a crash.
- 2026-10-14FDA-DeviceIntellijoint Surgical, Inc.Class IIIntellijoint Surgical navigation systems recalled for battery fire risk
Intellijoint Surgical's orthopedic navigation workstations may contain a 15-inch MacBook Pro battery that is subject to an Apple recall. The battery may overheat and pose a fire safety risk during use in surgical settings.
- 2026-10-14FDA-DeviceSteris CorporationClass IISteris HexaVue Focus system recalled for patient data mismatch on prints
A software issue in Steris HexaVue Focus Integration System (version 2.0.18) can cause incorrect patient information to appear on manually printed surgical images. This mismatch could lead to documentation errors or clinical images being linked to the wrong patient record.
- 2026-10-14FDA-DeviceLeMaitre Vascular, Inc.Class IILeMaitre TufTex embolectomy catheter recalled for balloon failure risk
LeMaitre Vascular's TufTex Over-the-Wire Embolectomy Catheter (Catalog Number E1651-88, Lot XOT00002181) failed internal testing. The balloon components can fail when exposed to pull force during use, which could compromise the device's ability to remove blood clots safely.
- 2026-10-14FDA-DeviceMindray DS USA, Inc.Class III8 productsMindray patient monitors recalled for unclear alarm manuals
Mindray is recalling 8 patient and telemetry monitor product lines because some operator's manuals may be insufficient or unclear about certain physiological alarm functions. The FDA classified this as a Class III recall, and no injuries have been reported. About 275,000 units are affected across the included models.
- 2026-10-14FDA-DeviceCanon Medical System, USA, INC.Class IICanon Medical Alphenix recalled for tabletop shift risk
Bolts that secure the longitudinal movement mechanism on the Canon Medical Alphenix INFX-8000C/B5 imaging system may loosen over time. This can cause the patient tabletop to shift unexpectedly, leading to misalignment during imaging procedures and motion errors.
- 2026-10-14FDA-DevicePOLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLCClass IIPolymedco SEDIPLAST tubes recalled for cap detachment risk
Certain Polymedco SEDIPLAST blood collection tubes (models S-100 and S-1000) may have a defect that causes increased resistance when a pipette is inserted. This pressure buildup can cause the tube cap to detach or be forcibly ejected, potentially exposing lab workers and work areas to blood.
- 2026-10-14FDA-DeviceAVID Medical, Inc.Class II15 productsAVID Medical surgical kits recalled for possible lubricant contamination
AVID Medical is recalling 15 surgical kits and packs, including DaVinci and Shands Jacks products, because they may be contaminated with a lubricant used during manufacturing. The recalled kits were distributed nationwide, with the listed states including AZ, CA, FL, MD, NE, and TX. No injuries have been reported.
- 2026-10-14FDA-DeviceOnkos Surgical, Inc.Class II2 productsOnkos Surgical pelvic implant recalled for patient mix-up
One personalized pelvic implant was shipped to the wrong customer due to a distribution error. The device is designed specifically for individual patients and should not be used by anyone other than the intended recipient.
- 2026-10-14FDA-DeviceNihon Kohden America LLCClass IINihon Kohden nurse station recalled for cybersecurity vulnerability
Nihon Kohden's CNS-6200 Series Central Nurse Station has a cybersecurity flaw that could allow someone to disrupt the system. If exploited, the flaw could prevent nurses from seeing patient monitoring data and alarms across multiple beds in a hospital.
- 2026-10-14FDA-DeviceMedtronic MiniMed, Inc.Class IIMedtronic MiniMed Flex pump recalled for failed quality tests
Some MiniMed Flex insulin pumps were shipped without completing required quality verification tests. These pumps may have problems including failure to work at startup, moisture damage, slow charging, connection issues with glucose monitors or the app, missed occlusion alerts, weak alarm sounds, or inaccurate insulin delivery.
- 2026-10-14FDA-DeviceMedline Industries, LPClass II2 productsMedline bariatric rollators recalled for front wheel detachment risk
Medline is recalling two bariatric basic steel rollator walkers, 2,659 units in total. The front wheel assembly can disconnect from the frame, causing the front wheels to become loose or detach during use, which could lead to falls and serious injuries such as head trauma or fractures. No injuries have been reported, and the products were distributed nationwide in the US and to Canada.
- 2026-10-14FDA-DeviceStryker Sustainability SolutionsClass IIStryker BARD EP XT catheter recalled for sterile barrier breach
Stryker Sustainability Solutions is recalling a specific lot of BARD EP XT Decapolar Steerable diagnostic catheters (Reference 201007) used in heart rhythm procedures. Some units may have a compromised sterile barrier on the primary pouch packaging, which could allow contamination if the catheter is used. This poses a risk of particle buildup, infection, or blood clots.
- 2026-10-14FDA-DeviceBeckman Coulter Inc.Class II2 productsBeckman Coulter DxC 500i analyzers recalled for falsely elevated results risk
Beckman Coulter identified a software issue in its DxC 500i and DxC 500 AU Clinical Chemistry Analyzers used for testing plasma samples. After a user changes a test to non-default units and later activates a configuration change, the analyzer may revert to the default units without warning, which can lead to falsely elevated reported results. The recall covers 2 product groups with 6 modules and analyzers in total.
- 2026-10-14FDA-DeviceDRG International, Inc.Class IIDRG International Sperm Ab ELISA recalled for false negative results
DRG International's Sperm Ab ELISA test (model EIA-1826) may return false negative results, meaning it could fail to detect sperm antibodies when they are actually present. This affects lot 320K046 distributed worldwide, including the US and multiple countries in Europe and Asia.
- 2026-10-14FDA-DeviceSafeguard US Operating LLCClass IISafeguard US compression bandages recalled for degradation risk
Safeguard US compression bandages used in trauma kits and first aid bags may degrade over time, potentially allowing foreign material to enter a wound. This degradation could require additional wound cleaning and may increase the risk of infection or scar tissue formation.
- 2026-10-14FDA-DeviceLimitless Cryo Spa LLCClass IILimitless Cryo Spa Glypto device recalled, lacks FDA clearance
Limitless Cryo Spa LLC distributed Glypto cryo machines without obtaining required FDA 510(k) clearance. The devices were supplied to facilities nationwide. No injuries have been reported.
- 2026-10-14FDA-DeviceCardinal Health 200, LLCClass IIMedtronic Microstream intubation kits need updated instructions
Cardinal Health Presource Packs contain Medtronic Microstream components that may be difficult to disconnect from a patient's breathing tube. Medtronic has updated the instructions for these kits to address this issue. The difficulty could delay treatment or cause unintended removal of the tube, potentially leading to serious breathing complications.
- 2026-10-14FDA-DevicePHILIPS MEDICAL SYSTEMSClass IIPhilips Spectral CT recalled for software image and motion issues
Philips Medical Systems has recalled certain Spectral CT and Spectral CT 7500 RT imaging systems due to software problems. These issues may cause image artifacts, incorrect slice thickness, or unintended movement of the system during operation.
- 2026-10-14FDA-DeviceGRI Medical & Electronic Technology Co., Ltd.Class IIHALYARD laparoscopy packs recalled for undeclared latex catheter
HALYARD Laparoscopy Comprehensive Pack II (REF: 49332) was labeled as "latex free" but contained a latex urethral catheter. This mislabeling poses a risk to patients with latex allergies who may use the kit. The recall affects 396 kits with specific lot numbers distributed nationwide.
- 2026-10-14FDA-DeviceQUANTUM OPS IncClass IIQUANTUM OPS Beach Chair positioner recalled for weld defect
QUANTUM OPS ADAPTABLE Beach Chair surgical positioners contain an inadequate weld in the patient head positioning system (BC-0105 subcomponent). This manufacturing defect could potentially affect the stability and safety of the device during surgical procedures. The defect was identified in specific lot numbers distributed in California and Texas.
- 2026-10-14FDA-DeviceSteris CorporationClass II6 productsSteris VERIFY biological indicators recalled for spore shelf-life issue
Steris is recalling six VERIFY biological indicator and challenge pack products used to monitor steam sterilization cycles. The spore population in these products may fall below its minimum shelf-life specification, so an indicator could show no growth even when a steam cycle did not achieve the intended spore reduction. No injuries have been reported.
- 2026-10-14FDA-DeviceMedical Action Industries, Inc. 306Class IIIMedical Action Industries urine collection kit recalled for labeling error
A data-entry error caused one lot of Medical Action Industries' urinary clean-catch collection kits to be labeled with an expiration date of March 31, 2027, when the correct date is February 28, 2027. This means the kits could be used beyond their intended shelf life, potentially affecting test reliability.
- 2026-10-14FDA-FoodJ K Patisserie & Bakery LLCClass II3 productsJ K Patisserie baked goods recalled for undeclared soy
J K Patisserie & Bakery is recalling 3 baked goods sold in cardboard boxes in New York and New Jersey: Lemon Blueberry Loaf, Chocolate Chip Cookies, and Croissants. The ingredient lists include soybean oil and soy lecithin, but soy is not listed in the allergen statement, so people with soy allergies could be at risk without knowing it. No injuries have been reported.
- 2026-10-14FDA-FoodSaint Francis Apizza LLCClass II4 productsSaint Francis Apizza frozen pizzas recalled for undeclared soy
Saint Francis Apizza is recalling four 17 oz. frozen pizzas sold in Kentucky and Ohio because they contain soybean oil and soy lecithin that are not listed on the label. People with soy allergies could react if they eat them. No illnesses or injuries have been reported.
- 2026-10-14FDA-FoodSWEET SENSIClass IISweet Sensi gum drops recalled for bacterial contamination
Sweet Sensi Elevated Edibles Hybrid Gum Drops in Passion Guava Kush flavor (Batch #1811) have been found to contain Staphylococcus aureus bacteria. The affected products are sold in 10-count and 30-count pouches nationwide.
- 2026-10-14FDA-FoodA&P CREATIONSClass I2 productsX10 and biQ-FEL supplements recalled for undeclared sildenafil and tadalafil
A&P Creations is recalling two products that contain sildenafil and tadalafil, prescription ingredients not listed on the label. The products are X10 Natural Enhancement Supplement, distributed by Natur Fuel, and biQ-FEL, distributed by Biofel. About 1,283 retail units of X10 and 3,116 bottles of biQ-FEL were distributed nationwide. No injuries have been reported.
- 2026-10-14FDA-FoodQUESO PALMITA GP LLCClass IIQueso Palmita cheese pie recalled for undeclared milk
Queso Palmita Pastel de Queso (Cheese Pie) contains milk that is not declared on the label. The product was distributed in Texas. People with milk allergies or sensitivities who consume this product could have a serious allergic reaction.
- 2026-10-14FDA-FoodGIAS FOOD INC.Class Ibettergoods Lemon Alfredo Fettuccine recalled for Listeria risk
bettergoods Lemon Alfredo Fettuccine pasta, distributed by Walmart, has been recalled because it may be contaminated with Listeria monocytogenes, a bacterium that can cause serious infection. The affected product is packed in a yellow sealed bag with a best-by date of September 21, 2027.