Safety Recalls
RSS ↗15,186 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 2,951–3,000 of 15,186
- Unclassified
Consumer Product Recall · December 11, 2025
Hunan Suihuo E-commerce Co., Ltd., dba BaoD, of China
Uuoeebb Infant WalkersThe recalled infant walkers violate the mandatory standard for infant walkers because they can fit through a standard doorway and fail to stop at the edge of a step, posing a deadly fall hazard. In addition, the infant walkers have leg openings that allow the child to slip down until the child's head can become entrapped, posing a risk of serious injury or death.
- Class II
Medical Device Recall · December 10, 2025
Mazor X robotic guidance system REF: TPL0059Software errors that can result in incorrect surgical instrument positioning during spinal surgery.
- Class II
Medical Device Recall · December 10, 2025
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
SMV BodyTrack, System, Tomography, Computed, EmissionGE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
- Class II
Food Recall · December 10, 2025
Publix Raspberry Coffee Cake, Net Wt. 15 oz. (425g), packaged in an aluminum foil tray and clear plastic clamshell lid with wraparound label, UPC 0-41415-54691-2, Distributed By Publix Supermarkets, IUndeclared allergen - walnuts. Maple Walnut Coffee Cake was incorrectly labeled as Raspberry Coffee Cake and walnuts were not declared on the label.
- Class II
Medical Device Recall · December 10, 2025
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
SMV DSX New Line, System, Tomography, Computed, EmissionGE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
- Class II
Medical Device Recall · December 10, 2025
MOSAIQ Oncology Information System with Particle Therapy License (License Kit 45700000000IQRO)Using oncology information system that manages workflow may result in overtreatment if:Plan delivered with Particle Therapy IHE-RO TDW-II interface,With one field per fraction or last field partial treatment,Partial treatment occurs followed by treatment field interruptions with manually recorded partial treatment,Then treatment unit doesn't check meterset value so partial treatment delivered twice
- Class II
Medical Device Recall · December 10, 2025
Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a physiciSome of the Calibration/Output Certificates had the outputs reversed.
- Class II
Medical Device Recall · December 10, 2025
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
MAXXUS, System, Tomography, Computed, EmissionGE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
- Class I
Food Recall · December 10, 2025
White Castle Original Sliders, Net Wt. 6.35 oz. (180g), packaged as a 4-count carton, each containing 2-Two Packs. UPC 082988029693, packed 6 cartons per case.Undeclared allergens (milk and soy).
- Class II
Medical Device Recall · December 10, 2025
MAVERICK¿ Measurement Module Spectrometer PN 820-01367 (originally part of a kit PN 820-01519) Finished Goods PN 820-01496Potential Elevated Laser Output A disconnected cable or a poorly crimped cable under mechanical bending stress can cause loss of electrical contact. At one connection on the board, the failure can drive the laser output to approximately 1,600 mW. Potential Unintended Laser Firing A disconnected, or poorly crimped cable can falsely signal a fire command during measurement cycles. At a secondary location on the board, this fault can lead to unexpected laser activation during operation. Safety logic prevents firing when the system is idle.
- Class II
Medical Device Recall · December 10, 2025
GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
SMV DSI, System, Tomography, Computed, EmissionGE HealthCare has become aware that certain Nuclear Medicine systems that are past the End of Guaranteed Service (herein referred to as Impacted Systems and listed in the Affected Product Details section of this letter) could have been transported or relocated without adequate detector support. This could result in excessive stress being applied to the detector mounting mechanisms, compromising their integrity. If this occurs, it can potentially result in a detector fall and lead to life-threatening bodily injury. There have been no reports of detector falls or injuries as a result of this potential issue. The Impacted Systems affected by this notice are those that have not been manufactured for several years. GE HealthCare has previously communicated End of Guaranteed Service for these Impacted Systems.
- Class II
Medical Device Recall · December 9, 2025
Heraeus Medical GmbH (Dental Division)
Brand Name: PALACOS Product Name: PALACOS MV+G pro 40; PALACOS MV+G pro 80 Model/Catalog Number: 5081290; 5081291 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-bincrease of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
- Class II
Medical Device Recall · December 9, 2025
Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWristDue to increased complaints for broken/frayed grip cables for reusable instruments.
- Unclassified
Vehicle Recall · December 9, 2025
2025 HYUNDAI IONIQ 5A loss of vehicle stability control increases the risk of a crash.
- Class II
Medical Device Recall · December 9, 2025
Heraeus Medical GmbH (Dental Division)
Brand Name: PALACOS Product Name: PALACOS MV pro 40; PALACOS MV pro 80 Model/Catalog Number: 5150633; 5150635 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-basedincrease of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
- Class II
Medical Device Recall · December 9, 2025
Heraeus Medical GmbH (Dental Division)
Brand Name: PALACOS Product Name: PALACOS R+G pro 40; PALACOS R+G pro 80 Model/Catalog Number: 5081288; 5081289 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-basincrease of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
- Unclassified
Vehicle Recall · December 9, 2025
2023 HYUNDAI IONIQ 6, 2024 HYUNDAI IONIQ 6, 2025 HYUNDAI IONIQ 6A detached charging port door panel can create a road hazard for other vehicles, increasing the risk of a crash.
- Unclassified
Vehicle Recall · December 9, 2025
2023 HYUNDAI PALISADE, 2024 HYUNDAI PALISADE, 2025 HYUNDAI PALISADESeat belt buckles that fail to latch may not properly restrain occupants in a crash, increasing the risk of injury.
- Class II
Drug Recall · December 9, 2025
Ciclopirox Shampoo, 1%, 120 mL, Rx only, Mfg by: Taro Pharmaceuticals Inc., Ontario, Canada; Dist. by: Taro Pharmaceuticals USA, Inc., NY 10532. NDC 51672-1351-08Failed Impurity/Degradation specifications: OOS results obtained at the 18-month timepoint
- Unclassified
Vehicle Recall · December 9, 2025
Daimler Trucks North America, LLC
2025 FREIGHTLINER CASCADIA, 2025 FREIGHTLINER BUSINESS CLASS M2, 2025 WESTERN STAR 47X, 2026 FREIGHTLINER CASCADIAA loss of vehicle steering control increases the risk of a crash.
- Unclassified
Vehicle Recall · December 9, 2025
2026 FOREST RIVER SPIRITElectrical arcing increases the risk of a fire.
- Class II
Medical Device Recall · December 9, 2025
Brand Name: da Vinci S, Si Tenaculum Forceps Instrument Product Name: da Vinci S, Si Tenaculum Forceps Instrument Model/Catalog Number: 420207 Software Version: N/A Product Description: EndoWristDue to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
- Class II
Medical Device Recall · December 9, 2025
Brand Name: da Vinci S, Si Grasping Retractor Instrument Product Name: da Vinci S, Si Grasping Retractor Instrument Model/Catalog Number: 420278 Software Version: NA Product Description: EndoWristDue to increased complaints for broken/frayed grip cables for reusable instruments.
- Class II
Medical Device Recall · December 9, 2025
Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved Scissors Instrument Model/Catalog Number: 420179 Software Version: N/A Product DescDue to increased complaints for broken/frayed grip cables for reusable instruments.
- Class II
Medical Device Recall · December 9, 2025
Brand Name: da Vinci S, Si Double Fenestrated Grasper Instrument Product Name: da Vinci S, Si Double Fenestrated Grasper Instrument Model/Catalog Number: 420189 Software Version: NA Product DescriDue to increased complaints for broken/frayed grip cables for reusable instruments.
- Class II
Medical Device Recall · December 9, 2025
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EDue to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments
- Class II
Medical Device Recall · December 9, 2025
Heraeus Medical GmbH (Dental Division)
Brand Name: PALACOS Product Name: PALACOS R pro 40; PALACOS R pro 80 Model/Catalog Number: 5081286; 5081287 Software Version: N/A Product Description: Radiopaque, poly(methyl methacrylate)-based (increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an impact on the ampoule breakage. An unfortunate combination of these influence factors can lead to unbreakable ampoules. If none or not all ampoules break, the product cannot be used on the patient since no or no appropriate cement dough is formed.
- Unclassified
Vehicle Recall · December 9, 2025
Daimler Trucks North America, LLC
2025 FREIGHTLINER CASCADIA, 2025 FREIGHTLINER BUSINESS CLASS M2, 2025 WESTERN STAR 47X, 2026 FREIGHTLINER CASCADIAA loss of brake function can increase the risk of a crash. In addition, a damaged wheel or tire can lead to a loss of vehicle control, increasing the risk of a crash.
- Class II
Food Recall · December 8, 2025
Goldenroot Lemon Double Ginger, Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32819 1. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
- Class II
Food Recall · December 8, 2025
MEAL SIMPLE RED LENTIL DAL SOUP NET WT. 16 OZ (1 LB) 454g UPC 1 97870 07333 0 MADE WITH PRIDE AND CARE FOR H-E-B-, SAN ANTONIO, TEXAS 78204Undeclared Milk. Wrong product in container.
- Class II
Food Recall · December 8, 2025
Goldenroot Lemon Ginger Hibiscus Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32821 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
- Class II
Medical Device Recall · December 8, 2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. AzurionNine (9) identified software issues which may result in the following: loss of X-ray after Pedal Tap, loss of X-ray after Phase Fault, missing live X-ray on the FlexVision monitor, system continues to restart, AMD triple drive, C-Partition of Suite PC running out of free space, system remains in continuous restart mode after start-up, misalignment of Marker Tool Overlay, longitudinal position error.
- Unclassified
Vehicle Recall · December 8, 2025
2025 IC BUS CESBA parking brake that is not engaged as expected when the driver releases the brakes may allow the vehicle to rollaway, increasing the risk of crash.
- Class II
Drug Recall · December 8, 2025
ORL Kids Mouthwash, Bubblegum Flavor, 16.9 oz. (500ml) per bottle, ORL Labs, LLC, Scottsdale, Arizona USAcGMP Deviations
- Class II
Medical Device Recall · December 8, 2025
Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.
- Class II
Drug Recall · December 8, 2025
ORL Kids Natural Toothpaste, Bubblegum Flavor, 4 oz (120ml), ORL Labs, LLC, Scottsdale, Arizona USAcGMP Deviations
- Class II
Medical Device Recall · December 8, 2025
Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3Securitas Healthcare has become aware of a firmware issue in the Call Stations in the Affected Lots that may cause Call Stations in the Affected Lots to (1) not transmit a low battery alert to the Arial Wireless Emergency Call System prior to battery failure, or (2) not transmit a low battery alert to the Arial Wireless Emergency Call system at least seven (7) days prior to the battery failing.
- Class II
Food Recall · December 8, 2025
Goldenroot Lemon Ginger Elderberry Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32818 4. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
- Class II
Medical Device Recall · December 8, 2025
The LDL-Cholesterol assay is comprised of two distinct phases. In phase one a unique detergent solubilizes cholesterol from non-LDL- lipoprotein particles. This cholesterol is consumed by cholesterolBeckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL Cholesterol reagent showed clinically significant interference due to triglyceride concentration up to 1500 mg/dL may cause a maximum positive bias of up to 28.8% in low LDL Cholesterol samples (concentration 80 mg/dL) and up to 11.02% in high LDL Cholesterol samples (concentration 160mg/dL).
- Class II
Medical Device Recall · December 8, 2025
Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 119629-000, 119630-000, 113803-000, 113803-600, 113802-000, 113802-600 Software Version: Not ApplicablTorque screw may crack or separate. If used, an affected screw could lead to inadequate head stabilization, compromised surgical precision, procedural delays, requirement for alternate head fixation methods, and risk of patient injury.
- Class II
Food Recall · December 8, 2025
Goldenroot Lemon Ginger Jalapeno Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32820 7. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
- Class I
Food Recall · December 8, 2025
Sam Dry Fruits and Nuts Enterprises, Inc
Sam Dry Fruits & Nuts PISTACHIO Meats Whole LOT #: PK00459 NET WEIGHT: 30 LBS PACK DATE: AUGUST/2025 EXPIRATION DATE: AUGUST/2027Potential contamination with Salmonella.
- Class II
Food Recall · December 8, 2025
Goldenroot Yuzu Ginger Lemongrass Ginger Beer. 12 oz. (355 ml) UPC 8 50052-32817 7. Keep Cold. Manufactured By Goldenroot, 3841 Market St #113, Denton, TX 76209.Ginger Beer products might contain ginger juice that did not undergo the required pasteurization process.
- Unclassified
Vehicle Recall · December 6, 2025
Honda (American Honda Motor Co.)
2023 ACURA MDX, 2023 ACURA TLX, 2023 HONDA PILOT, 2024 ACURA MDX, 2024 ACURA TLX, 2024 HONDA PILOT, 2025 ACURA MDX, 2025 ACURA TLX, 2025 HONDA PILOTA brake pedal that shifts out of position can prevent the driver from applying the brakes as intended, increasing the risk of a crash or injury.
- Class II
Food Recall · December 6, 2025
McCafe Premium Roast Decaf Coffee K-Cup Pods, Net Wt. 29 oz (823g), packaged as an 84-count carton, UPC 043000073438. Distributed By: Keurig Green Mountain, Inc. Burlington, MA 01803 U.S.A.Product is labeled as decaf, but might contain caffeine.
- Unclassified
Vehicle Recall · December 6, 2025
2024 DODGE CHARGER EV, 2025 DODGE CHARGER EVA vehicle that does not emit sound may fail to alert pedestrians of a moving vehicle, increasing the risk of a crash or injury.
- Unclassified
Vehicle Recall · December 6, 2025
2023 CHEVROLET SILVERADO 5500, 2023 CHEVROLET SILVERADO 4500, 2024 CHEVROLET SILVERADO 5500, 2024 CHEVROLET SILVERADO 6500An electrical short in the brake pressure switch can overheat the circuit and increase the risk of a fire while driving or parked.
- Unclassified
Vehicle Recall · December 6, 2025
2023 CHRYSLER VOYAGER, 2023 CHRYSLER PACIFICAA rearview image that does not display reduces the driver's view of what is behind the vehicle, increasing the risk of a crash.
- Class II
Medical Device Recall · December 5, 2025
Revogene C. difficile, in vitro diagnostic assay intended for use with the Revogene instrument, Catalog Number 410300The affected lots show a decline in performance over time, which may lead to false-negative results.
- Class II
Medical Device Recall · December 5, 2025
Siemens Medical Solutions USA, Inc
LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471A potential issue associated with LUMINOS Lotus Max and Luminos dRF Max systems with software version VF11 with bucky wall stand for mobile detectors and without ceiling stand .When switching quickly between organ programs (OGPs) the collimation may be incorrect.