Safety Recalls
RSS ↗15,379 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 12,301–12,350 of 15,379
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 8X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 4-7X70, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
Sonalleve MR HIFU 3.0T - Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781361The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
- Class II
Medical Device Recall · May 3, 2024
Achieva 1.5T Initial system Model Number (REF): 781178The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
- Class II
Medical Device Recall · May 3, 2024
Intera 1.5T- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781295The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 8X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 7X50, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 4-7X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 4-7X80, 1GDS, FH, TPR-TW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 5-8X45, 1GDS, NH, TPR-SW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 8X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 8X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 6X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 8X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
Panorama HFO- Magnetic Resonance (MR) systems are Medical Electrical Systems indicated for use as a diagnostic device. Model Number (REF): 781350The g-MDU (global Mains Distribution Unit) L3 terminal connection may become loose creating a hotspot that may cause smoke/fire to alarm in the hospital's technical room, resulting in Smoke and/or fire
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 6X40, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
Brand Name: Cerene Cryotherapy Device Product Name: DEVICE, THERMAL ABLATION, ENDOMETRIAL Model/Catalog Number: FGS-7000 Product Description: The Cerene Cryotherapy Device is an endometrial ablatioError code 003 was not listed in certain rows of the Device Instructions for Use Troubleshooting section (i.e., Table 22. Summary of LCD Messages and Error Codes).
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 6X45, 1GDS, CH, STR-SW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 6X40, 1GDS, FH, STR-SW. Single-Ended Slider GDS. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Class II
Medical Device Recall · May 3, 2024
ADVANTA VXT, 6X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graftComplaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
- Unclassified
Consumer Product Recall · May 2, 2024
Arctic Cat, of Thief River Falls, Minnesota
Arctic Cat 8000 and 9000 Series SnowmobilesThe recalled snowmobile's drive clutch can break, allowing fragments to escape the snowmobile shielding, posing a laceration hazard.
- Class II
- Class II
Medical Device Recall · May 2, 2024
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SWGE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner screen rather than the intended patient selected by the user.
- Class II
Food Recall · May 2, 2024
Rise Baking Company dba South Coast Baking
Costco Chocolate Chunk Frozen Cookie Dough, Net Wt. 33lb (14.97kg), 1.6 oz dough pucks Member's Mark Chocolate Chunk, Net Wt. 14.85lb (6.74kg), 144/1.65 oz dough pucks/case Panera Chocolate Chipper CPotential Salmonella contamination
- Class II
Medical Device Recall · May 2, 2024
GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DAGE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner screen rather than the intended patient selected by the user.
- Class II
Food Recall · May 2, 2024
Rise Baking Company dba South Coast Baking
Panera Oatmeal Raisin with Berries Cookie, Net Wt. 41.25 lb (18.71kg), 220/3 oz cookie dough pucks/casePotential Salmonella contamination
- Class II
- Unclassified
Consumer Product Recall · May 2, 2024
Polaris Industries Inc., of Medina, Minnesota
Model Year 2024 Prostar S4 Titan Adventure 155 ES SnowmobilesThe snowmobile can leak fuel at the pump flange assembly, posing a fire hazard and risk of serious injury to the rider or passenger.
- Unclassified
Consumer Product Recall · May 2, 2024
Mill Valley Jr. six-drawer youth dressersThe recalled dressers are unstable if they are not properly anchored to the wall, posing serious tip-over and entrapment hazards that can result in injuries or death to children. The dressers violate the performance requirements of the STURDY Act.
- Class II
- Unclassified
Consumer Product Recall · May 2, 2024
Dixon Ticonderoga Company, of Appleton, Wisconsin
Creativity Street Foam Pattern RollersThe recalled foam pattern rollers are intended for children and contain levels of lead that exceed the federal lead content ban in the rollers' handles. Lead is toxic if ingested by young children and can cause adverse health effects.
- Unclassified
Consumer Product Recall · May 2, 2024
Bausch & Lomb Americas Inc., of Bridgewater, New Jersey
Project Watson Eyelid Wipes for DogsWhen the recalled dog eyelid wipes are opened and in use, bacteria and fungi, which are organisms found widely in the environment, soil, and water, can be introduced and grow in the container, posing a risk of serious infection to people with weakened immune systems. Individuals with wounds may also be at higher risk of infection. People with healthy immune systems are not typically affected.
- Unclassified
Consumer Product Recall · May 2, 2024
Igloo Products Corp., of Katy, Texas
Youth Sipper BottlesThe silicone cover on the sipper can detach while in use, posing a choking hazard to children.
- Unclassified
Consumer Product Recall · May 2, 2024
Skims Body Inc., of Los Angeles, California
SKIMS Children's Pajama SetsThe children's pajama sets fail to meet the flammability regulations for children's sleepwear, posing a risk of burn injuries to children.
- Unclassified
Consumer Product Recall · May 2, 2024
Secop GmbH, of Germany (compressors
Commercial Refrigerators with Secop CompressorsThe recalled commercial refrigerators with Secop Compressors can fail in a manner causing the compressor to overheat, posing a fire hazard.
- Class I
Food Recall · May 2, 2024
Newly Weds Foods, LLC S07548 Starch WPC Blend 30lb bagPotential Salmonella contamination - ingredient
- Class I
Food Recall · May 2, 2024
PLANTERS¿ Honey Roasted Peanuts 4oz UPC 2900002097. Packaged in a flexible film package. 12 packages per case.Possible contamination with Listeria monocytogenes
- Class II
Food Recall · May 2, 2024
Rise Baking Company dba South Coast Baking
Rise Baking Company Cowboy Cookie, Net Wt. 18.75 lb (8.5 kg), 300/ 1.0 oz dough pucks/casePotential Salmonella contamination
- Class II
- Class II
- Class II
Food Recall · May 2, 2024
Rise Baking Company dba South Coast Baking
Panera Kitchen Sink Cookie, Net Wt. 45 lb (20.41 kg), 120/6 oz dough pucks/casePotential Salmonella contamination
- Class II
Drug Recall · May 2, 2024
TraMADol HCl 50 mg Tablet, Packaged as (a) 30-count blister pack, NDC 70518-3824-00; (b) 90-count blister pack, NDC 70518-3824-02; (a) 180-count blister pack, NDC 70518-3824-03; RX ONLY, MFG: AdvagenPresence of Foreign Tablets: Manufacturer received a report from a Pharmacist who reported finding a tablet of baclofen in a bottle of 1000-count tramadol
- Class I
Food Recall · May 2, 2024
Newly Weds Foods, LLC A51638 Breader X7 50lb bagPotential Salmonella contamination - ingredient
- Class II
Medical Device Recall · May 2, 2024
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasive investigation of cardiac and vascular diseases.Potential for pressure wave data synchronization from two devices may not be correct.
- Class II
- Class II
Medical Device Recall · May 2, 2024
BD Pyxis: MedStation ES (Main), REF: 323; MedStation ES Tower, REF: 352; Anesthesia Station ES, REF: 327; CII Safe ES, REF: 1116-00; CII Safe ES, Desktop PC, Wired Scanner, REF: 107-254-01; CII SIf automated dispensing cabinets have specific software versions, and Component Manager was configured to "installed mode", and software patch KB 5033688 was installed in the production environment, then this will will lead to an error that prevents the user from accessing the dispensing software application, which may delay accessing medication.
- Unclassified
Consumer Product Recall · May 2, 2024
American Honda Motor Co. Inc., of Torrance, California
Honda Lawnmowers, Replacement Engines, and Pressure Washers EnginesThe improperly manufactured camshafts in the engines can cause the starter rope to suddenly retract when pulling to start, posing an injury hazard.
- Unclassified
Consumer Product Recall · May 2, 2024
Generac Power Systems Inc., of Waukesha, Wisconsin
Walk-Behind Leaf Blowers and Vacuums, and Tow-Behind Leaf VacuumsPieces from the recalled leaf blowers and vacuums can come loose inside the unit and be ejected, posing a laceration hazard to users and bystanders.
- Class II