Archive
704 recalls were announced in September 2024.
Of the 704 recalls this month scored against our rubric, 1% are Critical, 14% are Severe.
Which agencies issued them
Nova Bus is recalling certain 2022-2023 LFS buses because a software error may cause the Vehicle Control Unit to crash, disconnecting the high voltage batteries and causing a loss of drive power.
Bombardier is recalling 2017-2019 Can-Am Spyder RT and F3 motorcycles because the engine output shaft may break, causing a loss of drive power and increasing crash risk.
Audi is recalling certain 2022-2024 e-tron GT and RS e-tron GT vehicles because the high-voltage battery may experience a short circuit within the battery module, increasing fire risk.
Mercedes-Benz is recalling 2021-2022 GLE 350 and GLE 450 vehicles because an incorrectly routed wiring harness may prevent front air bags from deploying properly.
Volkswagen is recalling certain 2024 Atlas and Atlas Cross Sport vehicles because the brake master cylinder may have an incorrect secondary piston spring retainer that can block the brake fluid port.
Pork Dynasty Inc. is recalling approximately 469 pounds of ready-to-eat fried pork skin products because they contain soy, a known allergen, that is not declared on the label.
Chrysler is recalling certain 2020-2024 Wrangler 4XE and 2022-2024 Grand Cherokee 4XE vehicles because the high voltage battery may fail internally and cause a fire while parked or driving.
Chrysler is recalling specific Mopar Hybrid Service Kit Battery Packs because they may fail internally and cause a fire. Owners should park outside and not recharge until repaired.
Forest River is recalling 2024-2025 Viking and Clipper travel trailers because roof rack hardware may not be properly tightened, posing a road hazard risk.
Royal Enfield is recalling certain 2023 Himalayan, Classic 350, Meteor 350, Hunter 350, Super Meteor 650, Int 650 and Continental GT 650 motorcycles whose side and rear reflectors fail FMVSS 108.
Forest River is recalling 2024-2025 Viking and Clipper travel trailers because side marker lights may not reflect light properly, reducing visibility to other drivers.
Ford is recalling certain 2024 F-53 and F-59 stripped chassis vehicles because the instrument panel cluster may not properly display the transmission gear position indicator, failing FMVSS 102.
EVject is recalling Escape Connector NACS v1.0 and v1.1 charging cable adaptors because they lack internal thermal protection, creating a risk of overheating and burn injury.
BMW is recalling certain 2021-2024 R18 motorcycles because the seal for the reverse gear control unit may deteriorate, allowing moisture inside and causing the unit to overheat.
Brinkley RV is recalling certain 2025 Model Z travel trailers because the installed safety chains are underrated for the Gross Vehicle Weight Rating. 40 units are affected.
Deere & Company is recalling about 147,900 John Deere 1023E, 1025R, and 2025R Compact Utility Tractors because the front bell crank in the brake linkage can fail, causing loss of braking and crash risk. Four failures have been reported, including one hospitalization and two impact injuries.
Tesla is recalling certain 2024 Cybertruck vehicles because the rearview camera image may be delayed after shifting into reverse, failing FMVSS 111. 27,185 units affected.
Chrysler is recalling 2024 Ram Promaster BEV vehicles because incorrect software may cause a loss of drive power, increasing crash risk.
Harley-Davidson is recalling 2018-2019 Softail FXBB and FXLR motorcycles because the front tire inflation pressure on the VIN label may be incorrect, potentially leading to tire overloading.
Liberty Hardware is recalling about 174,500 Multi-Grip Tub Safety Bars because plastic grip pads can become dislodged on tapered tubs, making the bars unstable and creating a fall hazard. One minor fall injury has been reported.
Baxter is recalling EXACTAMIX compounding device inlets due to particulate matter observed in sterile fluid pathways before use. Approximately 5.8 million units affected worldwide.
Tenneco is recalling aftermarket ball joints for 2013-2019 Ford Escape vehicles because they may separate, causing loss of steering control.
GBC Food Services is recalling Supreme brand guacamole and pico/guacamole products distributed in Indiana due to possible contamination with Listeria monocytogenes.
GBC Food Services, LLC is recalling multiple Supreme Peppers products distributed in Indiana due to possible contamination with Listeria Monocytogenes. Consumers should not consume these products.
Baxter Healthcare is recalling EXACTAMIX Inlet components (H938173 and related codes) due to particulate matter contamination observed in the sterile fluid path before use. Approximately 3.58 million units distributed worldwide are affected.
Baxter Healthcare Corporation is recalling EXACTAMIX Inlet components due to particulate matter found in sterile fluid path tubing. Approximately 1.5 million units were distributed worldwide.
BMW is recalling certain 2023-2024 228i, 228i xDrive and 2025 MINI Countryman S ALL4 vehicles because the bolts connecting the front body structure to the chassis may be loose.
BMW is recalling specific 2024-2025 models because the steering spindle may break, increasing steering effort and crash risk. Dealers will replace the joint free of charge.
BonBon NYC LLC is recalling Marabou Sea Salt Chocolate Bars due to undeclared almonds, wheat, and tree nuts. Consumers allergic to these ingredients should not consume the product.
Baxter Healthcare is recalling ExactaMix pharmaceutical compounding device inlets due to increased reports of particulate matter in the sterile fluid path before use. The recall involves 2,140,046 units with worldwide distribution.
Yummi Sushi is recalling Supreme vegetable products distributed in Indiana due to possible Listeria monocytogenes contamination. Consumers should not consume these products.
Bliss Tree Millet Butter Murukku products are being recalled due to undeclared sesame and milk allergens. Affected products were distributed to retailers and online customers in multiple states.
B Braun's STREAMLINE FRESENIUS bloodline tubing used in hemodialysis may have a design issue where incomplete insertion of the patient connector prevents proper blood flow during certain procedures. Patients receiving dialysis may experience treatment delays.
Safeguard US Operating LLC is recalling the HAWK Advanced Hypothermia Management Set due to incorrect expiration dates on affected units. The product may not perform reliably if used after the incorrect date.
Philips recalls Azurion X-ray imaging systems due to potential cable hose carrier detachment from broken plastic or bolts, which may cause parts to fall and create injury risk.
B. Braun Medical is recalling STREAMLINE LONG hemodialysis bloodline tubing because the patient connector may fail to fully insert into the Locksite, potentially causing blood flow obstruction during dialysis treatment.
Smith & Nephew issued a voluntary recall of K-Wire bone fixation fasteners due to a packaging error where packages contained the wrong wire diameter than labeled.
Philips Allura Xper FD series fluoroscopy systems may have detached cable hose carriers due to broken plastic or bolts. A detachment could cause parts to fall and potentially result in injury.
Cypress Medical Products recalls Acceava Respiratory Strep A diagnostic test kits nationwide due to a classification error that caused them to be shipped to customers without proper licensing.
MicroVention is recalling 1,370 ERIC Retrieval Devices due to labeling errors showing incorrect expiration dates (5 years instead of actual 3 years). Devices with mislabeled shelf life may be used beyond their true expiration.
B Braun Medical Inc. is recalling Streamline Bloodline Sets because incomplete connector insertion may cause flow restrictions during hemodialysis.
Bliss Tree Curry Leaves Butter Murukku is recalled due to undeclared milk. The product was distributed to retailers in CA, NJ, GA, AZ, MD, and nationwide online.
Boston Scientific is recalling 89 units of Flexima APDL Drainage Catheter Systems because holes in the sterile barrier may compromise device sterility.
Seer Home System ambulatory EEG devices were recalled due to electromagnetic compatibility non-compliance and manufacturing control deficiencies. The issue may affect signal recording reliability in home EEG monitoring.
Siemens Healthcare's ADVIA Chemistry Microalbumin diagnostic test may produce falsely low results. Eight lots do not meet High-Dose Hook Effect and Prozone Effect specifications, potentially affecting microalbumin detection accuracy.
Kodiak Cakes LLC is recalling 7,300 boxes of Kodiak Protein-Packed Power Waffles due to soft plastic film contamination. Consumers should not consume the affected product.
Endo retrieval pouches are recalled because the tube may detach and fall into the surgical site during use. Approximately 81,241 units distributed in Georgia, Missouri, and Pennsylvania are affected.
B. Braun is recalling approximately 4.98 million STREAMLINE FRESENIUS FOR DAVITA hemodialysis bloodline tubes due to risk of improper connector insertion, which could cause blood flow occlusion during dialysis treatment.
B Braun is recalling SL BLOODLINE FOR FMC 2008 SERIES hemodialysis tubing nationwide due to incomplete connector insertion that may cause blood flow restrictions during treatment.
Smith & Nephew is recalling K-Wire surgical devices due to a packaging error that resulted in wrong-sized wires being distributed. Healthcare providers may have received incorrectly sized bone fixation fasteners affecting approximately 73 units.
Boston Scientific is recalling Flexima Biliary Catheter System Kit (Lot #33512376) due to potential holes in the device pouch's sterile barrier, which could compromise device sterility. No illnesses or injuries have been reported.
Innovasis is recalling TxHA PEEK and TxTiHA IBF intervertebral fusion devices due to interfacing issues between the implant and inserter that may prevent proper placement. The recall affects 568 devices distributed nationwide.
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to undersized pneumatic tubing in the reagent storage module, which can cause air leaks and compressor failures, potentially leading to test errors and delayed results.
Medline is recalling 4,831 Contro-Bulb Syringes due to potential sterile barrier breach during transportation. The recall affects two lot numbers and applies nationwide.
Medtronic is recalling CareLink 2090 Programmers (serial number prefixes PKK0 and PKK1) worldwide due to potential autonomous cursor motion when Finger Touchscreen capability is enabled with software version 3.2 or higher. Approximately 18,788 units are affected.
CareFusion's Alaris System PC Unit Model 8015 infusion pumps are being recalled due to a bent female IUI connector affecting over 125,000 devices. The defect may prevent the device from operating properly or delay infusion or monitoring startup.
B. Braun Medical is recalling 19,050 AET36 Anesthesia Extension Sets due to potential product leakage from the Spin Lock Connector caused by excess solvent migration during manufacturing.
B Braun Medical is recalling hemodialysis bloodline tubing because the patient connector may not fully insert into the device, potentially blocking blood flow and delaying treatment. Affected units were distributed nationwide.
Mazor Robotics is recalling 94 Mazor X surgical navigation devices due to software errors that cause screen lag or screw-tracking mismatches during orthopedic procedures.
GE Healthcare ViewPoint 6 medical imaging systems contain a software vulnerability (CVE-2023-43208) in Mirth Connect that could allow unauthorized access and patient data manipulation. 574 units are affected and distributed nationwide.
GE Healthcare is recalling three ViewPoint imaging systems due to a software vulnerability in Mirth Connect that could allow unauthorized access and manipulation of patient data.
ROi CPS LLC is recalling medical convenience kits distributed with Merit syringes that were subsequently recalled by their manufacturer. Approximately 3,387 kits with multiple lot numbers were affected.
Boston Scientific is recalling Flexima Regular Kit Nephrostomy Catheter System kits due to potential holes in the sterile barrier pouch that may compromise device sterility.
Bliss Tree Moringa Butter Murukku 400g is recalled because it contains undeclared milk, a common food allergen. Consumers with milk allergies should not consume this product.
Boston Scientific is recalling VTC Regular Kit Nephrostomy Catheter System kits due to potential holes in the sterile barrier of the device pouch, which may compromise device sterility.
Bliss Tree Millet Butter Ribbon Pakoda is recalled because it contains undeclared milk. The product was distributed to retailers and wholesalers in five states and nationwide online.
CareFusion 303, Inc. recalls 180 Alaris EtCO2 Module Model 8300 units with potentially bent female connectors that may prevent device operation, risking delays in infusion and monitoring.
Flagstone Foods LLC is recalling Wegmans Pecan Blend because it contains undeclared almonds, a common allergen. The product was distributed to nine states: DC, DE, MA, MD, NC, NJ, NY, PA, and VA.
Bliss Tree Millet Butter is being recalled because it contains undeclared milk, a common allergen. The product was distributed to wholesalers and retailers in five states and to online customers nationwide.
PHILIPS medical X-ray imaging systems may have a cable hose carrier that can detach due to broken plastic or bolts, potentially causing parts to fall and injure clinical staff.
Carbon Medical Technologies is recalling the BiomarC EX Fiducial Marker System because patients did not receive the required MRI Insert component needed for safe use during MRI procedures.
Bliss Tree Ragi Butter Murukku 200g and 400g packages are recalled due to undeclared milk. Consumers with milk allergies should not consume these products and contact their retailer.
CareFusion recalls approximately 10,460 Alaris PCA Module Model 8120 infusion pumps worldwide due to potentially bent female IUI connectors that may prevent proper device operation and delay treatment initiation.
CareFusion's Alaris Syringe Module Model 8110 infusion pumps are being recalled because affected units may have bent female connectors that can prevent device operation and delay infusions. Approximately 20,145 units have been distributed worldwide.
Boston Scientific is recalling the vanSonnenberg Sump Catheter System Kit because the sterile barrier pouch may have holes that could compromise device sterility. The recall affects 4 units distributed in the US, Colombia, Philippines, and Russia.
Safeguard US Operating LLC is recalling the HAWK Warming Grid (Item 59-300) due to an incorrect expiration date. The affected units may not function safely if used beyond the actual expiration date.
B. Braun is recalling 9,864,165 Streamline Bloodline Sets nationwide due to incomplete patient connector insertion. The defect may restrict fluid flow during hemodialysis and cause therapy delays.
Tornier, Inc. is recalling one lot of the Stryker TORNIER PERFORM HUMERAL SYSTEM - STEMLESS shoulder implant due to bacterial endotoxin exceeding safety specifications. The 5 affected units were distributed in Illinois, Wisconsin, Arizona, Nevada, and South Dakota.
Siemens Healthcare Diagnostics is recalling Atellica CH and ADVIA Chemistry Microalbumin test kits worldwide because they may not properly measure microalbumin in urine samples, potentially causing falsely low results that could delay diagnosis of kidney disease.
CareFusion is recalling approximately 192,964 Alaris Pump Module Model 8100 infusion pumps that may have bent female connectors preventing device operation and delaying patient treatment.
Philips is recalling 109 MultiDiagnost Eleva X-ray systems worldwide due to potential cable hose carrier detachment from broken plastic or bolts, which could cause parts to fall and result in injury.
Cypress Medical Products is recalling BinaxNOW Respiratory Strep A Test Kits due to an inventory system error that resulted in shipment to customers without proper licensing to purchase medical devices.
GE Healthcare is recalling 803 units of the Centricity Universal Viewer Zero Footprint Client because the latest addended report may not display by default in specific browsers.
GM is recalling certain 2024 Buick Envision vehicles because they are missing the label stating tire size, pressure and loading information, failing FMVSS 110.
Marodyne-LiV low-intensity vibration exercisers with certain serial numbers are recalled due to a power supply voltage drop that unexpectedly interrupts treatment. Manual activation is required to restart the device.
Cypress Medical Products is recalling McKesson 60 mL syringes that lack FDA clearance. The syringes were inadvertently shipped from a distribution center due to an order processing error and were on quarantine.
Unomedical A/S is recalling specific VariSoft Infusion Sets packaged in boxes incorrectly branded as 'Trusteel Infusion Set' instead of 'VariSoft.' No injuries or illnesses have been reported.
Safeguard US Operating LLC is recalling 567 units of HAWK warming kits due to incorrect expiration date labeling. The kits were distributed nationwide in 16 states.
Rubicon Research Private Limited is recalling 3,984 bottles of Acetazolamide 125 mg tablets nationally due to discoloration. Affected lot is 30575HF1 with expiration November 2026.
Textron is recalling 1,137 low-speed vehicles because a brake linkage rod may bend, impairing braking ability and increasing crash risk.
Aston Martin is recalling certain 2024-2025 DBX707, DB12 and 2025 Vantage vehicles because the engine oil cooler hose may split, resulting in a loss of oil and oil pressure.
Cummins is recalling specific X15 diesel engines and fuel pump components because the fuel pump barrels may fracture and cause a fuel leak, leading to engine stalls.
Micro Bird is recalling 2023-2024 G5 school buses because a failing engine drive belt tensioner can cause power steering loss or engine overheating.
Micro Bird is recalling one 2023 G5 transit bus because a failing engine drive belt tensioner can cause a loose belt, leading to power steering loss or fire.
Toyota is recalling certain Corolla Hybrid and Corolla Cross Hybrid vehicles because a skid control ECU software error may result in a loss of power brake assist when cornering.
Mercedes-Benz is recalling 2021-2023 S 580 and Maybach S 580 vehicles because engine software may cause overheating or stalling, increasing crash and fire risks.
Triple E is recalling 2024 Unity and Wonder motorhomes because transposed weight rating labels could lead to vehicle overloading and increased crash risk.
Ceither Adult Portable Bed Rails sold on Amazon violate federal regulations and pose a serious risk of entrapment and asphyxiation. Users can become trapped within the bed rail or between the rail and mattress.
Lamborghini is recalling 39 2024 Huracan EVO Spyder vehicles because the right front frame bracket may be installed on the wrong side, potentially reducing crash protection.
General Motors is recalling 2013-2019 Chevrolet Express and GMC Savana Cutaway vans because brake lines may rub against body mounts, causing leaks and potential brake failure.
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