Safety Recalls
RSS ↗15,364 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 11,701–11,750 of 15,364
- Class II
Medical Device Recall · June 7, 2024
Rygel Advanced Machines d/b/a Omtech Laser
OMTech Desktop Laser EngraverLack of redundant interlocks, missing required labels and certification labels as required by 21 1010.2.
- Class II
Food Recall · June 7, 2024
Chef Select 2 Herb Baguettes Filled With Herb Butter 2x175 g Barcode: 4056489447566. Frozen product packaged in a plastic bag, 2 baguettes per unit.Undeclared wheat and milk (foreign language labeling)
- Class I
Medical Device Recall · June 7, 2024
smiths medical portex BLUperc Percutaneous Diliation Procedural Trays with BLUselect tracheostomy tubes, labeled as follows: 1) BLUperc Percutaneous Dilation Procedural Kit with Single Stage DilatoThere is the potential for a disconnection of the pilot balloon from the tracheostomy inflation line within specific lots of the BLUSelect, BLUgriggs and BLUperc products due to a manufacturing defect.
- Class I
Medical Device Recall · June 7, 2024
smiths medical portex BLUgriggs Percutaneous Dilation Procedural Trays with BLUselect tracheotomy tubes, labeled as follows: 1) BLUgriggs Percutaneous Dilation Procedural Tray with forceps and 8.0mThere is the potential for a disconnection of the pilot balloon from the tracheostomy inflation line within specific lots of the BLUSelect, BLUgriggs and BLUperc products due to a manufacturing defect.
- Unclassified
Consumer Product Recall · June 6, 2024
Good Earth Lighting Inc., of Mount Prospect, Illinois
Good Earth Rechargeable Integrated LightsThe recalled light's battery can overheat and ignite the light's plastic housing, posing fire and burn hazards to consumers.
- Unclassified
Consumer Product Recall · June 6, 2024
Sling CarriersThe recalled sling carriers violate the safety requirements of the Safety Standard for Sling Carriers, including requirements for structural integrity and occupant retention, posing a fall hazard to babies. Additionally, the sling carriers pose a suffocation hazard because they fail to meet the federal safety standard's requirements for restraint systems, as the waist restraint can be used without the crotch restraint. Further, there are no warnings or instructional literature providing information to caregivers about keeping the baby's face clear to prevent suffocation or safe positioning, to prevent the baby from curling into a position with their chin resting on or near their chest. Sling carriers manufactured after January 30, 2018 are subject to the mandatory federal safety standard.
- Class II
Food Recall · June 6, 2024
Red Button Vintage Creamery Cookie Dough Ice Cream, Net weight 1.75 qt (1.66 L).Foreign object, rubber, found in two tubs of Red Button Vintage Creamery Cookie Dough Ice Cream.
- Unclassified
Vehicle Recall · June 6, 2024
2023 TOYOTA HIGHLANDER, 2024 TOYOTA HIGHLANDERTires with an insufficient load rating may be overloaded and fail, increasing the risk of a crash.
- Unclassified
Vehicle Recall · June 6, 2024
2023 RAM 3500A loss of drive power or a loss of park function increase the risk of a crash.
- Unclassified
Vehicle Recall · June 6, 2024
2024 CHEVROLET CORVETTE, 2025 CHEVROLET CORVETTEAn inaccessible seat belt that cannot restrain an occupant, increases the risk of injury in a crash.
- Class I
Food Recall · June 6, 2024
Green Life Farms Baby Arugula in 4.5 ounce plastic clamshell packaging containers. 6 packages per case of 4.5oz each. Store in refrigerator.Salmonella contamination
- Class I
Food Recall · June 6, 2024
Arepas La Mejor, Arepa de Chocolo (Chocolate Sweet Corn Pancakes), NET WT. 25 Oz., 5 units per package, KEEP REFRIGERATEDUndeclared allergens: Milk
- Unclassified
Vehicle Recall · June 6, 2024
2023 RAM PROMASTER, 2024 RAM PROMASTERA missing side door beam may not provide adequate occupant protection in a crash, increasing the risk of injury. Incorrect seating capacity information can result in an improperly loaded vehicle, increasing the risk of injury in a crash.
- Unclassified
Consumer Product Recall · June 6, 2024
Kawasaki Motors Manufacturing Corp. U.S.A., of Maryville, Missouri
Kawasaki Engines used in Bad Boy Mowers, BigDog, Bobcat, Cub Cadet, Hustler, John Deere, and Kubota brand lawn and garden equipmentThe recalled engines can overheat, posing fire and burn hazards.
- Unclassified
Consumer Product Recall · June 6, 2024
Salewa USA LLC, of Boulder, Colorado
Wild Country Ropeman 1 ascendersThe teeth of the recalled ascenders can fail to engage, making it difficult or impossible for the user to ascend.
- Unclassified
Consumer Product Recall · June 6, 2024
Spectrum Brands Pet LLC, of Middleton, Wisconsin
FURminator deShedding Ultra Premium Dog Conditioner (1 Gallon)The recalled conditioner can contain bacteria, including Pseudomonas aeruginosa, an environmental organism found widely in soil and water. People with weakened immune systems or external medical devices who are exposed to Pseudomonas aeruginosa face a risk of serious infection that may require medical treatment. The bacteria can enter the body if inhaled, through the eyes, or through a break in the skin. People with healthy immune systems are usually not affected by the bacteria.
- Unclassified
Consumer Product Recall · June 6, 2024
SA Consumer Products Inc., of Rolling Meadows, Illinois
Sanctuary and Sports Afield Biometric Firearm SafesThe biometric lock on the gun safes can be opened by unauthorized users, posing a serious injury hazard and risk of death.
- Class I
Medical Device Recall · June 5, 2024
SENSE XL TORSO COIL 1.5T Mk2. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567502281, 453567502282, 453567502283, 45356750228Potential for coils to heat up and harm patients (burn).
- Class I
Drug Recall · June 5, 2024
STELLALIFE VEGA Oral Care, Spray, Unflavored, 1 fl oz (30 ml) bottles, Distributed by: StellaLife, 22875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-121-01Microbial Contamination of Non-Sterile Products: multiple Bacillus species organisms
- Class II
Medical Device Recall · June 5, 2024
Synergetics I Pack Injection Kit Custom-Tray for use with Ophthalmic injections Model/Catalog Number: 18069 Product Description:Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
- Class II
Medical Device Recall · June 5, 2024
Synergetics I-Pack Injection Kit with Drape -For use with Ophthalmic injections Model/Catalog Number: 18061Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
- Class II
Medical Device Recall · June 5, 2024
Synergetics I Pack Injection Kit with Wire Speculum- Tray for use in Opthalmic Injection Model/Catalog Number: 18069WCould not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
- Unclassified
Vehicle Recall · June 5, 2024
2024 MERCEDES-BENZ ESPRINTERExtended stopping distance can increase the risk of a crash.
- Class II
Medical Device Recall · June 5, 2024
Synergetics I Pack Injection Kit- Tray for use with Ophthalmic injections Model/Catalog Number: 18060Could not confirm products were exposed to the proper sterilization cycle can potentially cause post operative wound infection or injection site infection.
- Class II
Drug Recall · June 5, 2024
STELLALIFE ADVANCED FORMULA Peppermint, VEGA Oral Care, Rinse, 16 fl oz (473 ml), Distributed by: StellaLife, 2875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-143-16Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism
- Class II
Medical Device Recall · June 5, 2024
DxC 500 AU Clinical Chemistry Analyzer, REF C63520 is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate reagents, calibrators, quality control (QC)There are two software bug issues with the analyzer. Issue 1: When a dedicated rack is reserved for calibration, after a calibration test has been placed and completed, the same rack may be used to place both a patient order and a calibration order. When a patient sample and a non-barcoded calibrator tube is processed on the rack, the calibration result will be reported as a patient result. Issue 2: calibration with expired calibrator. They both may cause erroneous patient results, but the probability of serious adverse health consequences or death is unlikely.
- Class I
Medical Device Recall · June 5, 2024
SENSE XL TORSO COIL 1.5T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567141882, 453567141883. Coils may be included in kitsPotential for coils to heat up and harm patients (burn).
- Class I
Medical Device Recall · June 5, 2024
SENSE XL TORSO COIL 3.0T. 16-element receive only coil for torso and abdomen imaging in Philips MR Intera and Achieva Systems. Model Numbers: 453567394941, 453567394942, 453567394943, 453567394945, 45Potential for coils to heat up and harm patients (burn).
- Class III
Drug Recall · June 4, 2024
Dr. Reddy's Laboratories, Inc.
Eszopiclone Tablets, USP 1mg CIV, 30-count bottle, Rx only, Mfd. By: Dr. Reddy's Laboratories Limited, Bachupally - 500 090 INDIA, NDC 55111-629-30Failed Impurities/Degradation Specifications: Related Substances
- Class II
Medical Device Recall · June 4, 2024
Zyno Medical Z800, Z800F, Z800W, and Z800WF Infusion PumpsZyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps have faulty power supply modules that will not provide a charge to the rechargeable battery within the pump. This may lead to the battery having insufficient or no charge available to the pump when it is unplugged from the AC mains power.
- Class II
Medical Device Recall · June 4, 2024
Trulight 5000/3000 Surgical Light, model numbers: a) 4038210 (Duo Surgical Lights}; b) 4038310 (Trio/Quad Surgical Lights)Baxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted as they are equipped with iLED 7 light-heads
- Class II
Medical Device Recall · June 4, 2024
SEASPINE ORTHOPEDICS CORPORATION
Brand Name: Meridian Angled Awl Fixed Product Name: Angled Awl Fixed Model/Catalog Number: RA2-003015 Product Description: Surgical Awl Component: NoInsufficient weld around the cap component of the instrument is insufficient to withstand impaction forces.
- Class II
Medical Device Recall · June 4, 2024
iLED 7 surgical lights, Model Numbers: a) 4068110 (Ceiling Single Surgical Light); b) 4068120 (Mobile Surgical Light); c) 4068140 (Pendant Surgical Light); d) 4068210 (Ceiling Duo SurgicalBaxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted as they are equipped with iLED 7 light-heads
- Class II
Medical Device Recall · June 4, 2024
VidiaPort carrying arm, mount for auxiliary products, model numbers: a) 4028110 (Ceiling Single Surgical Light); b) 4028210 (Ceiling Duo Surgical Lights); c) 4028310 (Ceiling Trio Surgical LighBaxter Healthcare Corporation is issuing an Urgent Medical Device Correction due to customer reports of thermal skin injuries when using the iLED 7 surgical light system products listed below. Specific VidiaPort and Trulight product codes are also impacted as they are equipped with iLED 7 light-heads
- Class II
Medical Device Recall · June 4, 2024
Dxl 9000 Access Immunoassay Analyzer, Catalog #C11137.The analyzers were built with nonconforming USB cables made with brass contacts instead of specified gold contacts. Brass contacts may corrode over time, leading to loss of internal instrument communication and delayed patient results.
- Class I
Food Recall · June 3, 2024
Nature's Wonderland brand Thyroid Formula 60 Veg Capsules UPC: 715486893205. Packaged in White PET 150cc bottle with security closurePotential Salmonella contamination
- Class II
Medical Device Recall · June 3, 2024
Transfer Device, REF 2008S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
- Class II
Medical Device Recall · June 3, 2024
Endoscopic Kittner Blunt Dissecting Instrument, Intended to be used for blunt dissection of tissue, Model Number KT-9101The affected products may have been packaged with a defect in the sterile barrier seal. As a result, the integrity of the sterile barrier may be compromised.
- Class II
Medical Device Recall · June 3, 2024
Fresenius Medical Care Holdings, Inc.
RTLR190395: 2008K@HOME MACHINE, SHORT CAB,OLC/DP,HP - Blood Pump Rotor spare part, Model Number: F40015481 Rev AAn increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
- Class II
Medical Device Recall · June 3, 2024
Fresenius Medical Care Holdings, Inc.
RTL190904: 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part, Model Number: F40015481 Rev AAn increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
- Class II
Medical Device Recall · June 3, 2024
Bag Decanter II, REF 2002S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).During sterile barrier testing performed on the decanter product line, the samples were identified to have pin holes and tears in the packaging film.
- Class II
Medical Device Recall · June 3, 2024
Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the vertebral body in a curved configuration. This provides physicians with the abilExpired Products distributed to customers
- Class II
Medical Device Recall · June 3, 2024
This product is a single use sterile device that is used to direct the lesion to the targeted site. Each cannula contains a stylet that is removed once the cannula is placed. The electrode is then insExpired Products distributed to customers
- Class II
Medical Device Recall · June 3, 2024
QIAcube Connect MDx - IVD Instrument designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model/Catalog Number: 900Heater shaker module does not perform heating if the temperature is set below 40¿C for static incubation steps when running IVD protocol QIAamp¿ DSP DNA Mini Kit (cat. no. 61304), Protocol: Isolation of genomic DNA from Gram-positive bacteria (Script filename: Kt_name_Bacteria (Gram+) or rY'east_Enzymatic Lysis_ V2) which could potentially cause delayed or erroneous results depending on the downstream assay.
- Class II
Medical Device Recall · June 3, 2024
Fresenius Medical Care Holdings, Inc.
191014: 2008K@HOME HD SYSTEM W/BIBAG (CANADA) - Blood Pump Rotor spare part, Model Number: F40015481 Rev AAn increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
- Class II
Medical Device Recall · June 3, 2024
Fresenius Medical Care Holdings, Inc.
190904 2008K@HOME HEMODIALYSIS SYSTEM W/ BIBAG - Blood Pump Rotor spare part, Model Number: F40015481 Rev AAn increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
- Class II
Medical Device Recall · June 3, 2024
Fresenius Medical Care Holdings, Inc.
190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev AAn increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.
- Class I
Food Recall · June 3, 2024
Queso Rico La Hacienda brand queso fresco cheese packaged in 9 oz, 1 pound, and 2 pound plastic packages. Product labeling reads in part "***QUESO RICO LA HACIENDA***EL QUESO FRESCO FRESCO DE VERACRUQueso fresco was found to contain Listeria monocytogenes.
- Class II
Medical Device Recall · June 3, 2024
Fresenius Medical Care Holdings, Inc.
RTL190828: 2008K@HOME HEMODIALYSIS SYSTEM - Blood Pump Rotor spare part, Model Number: F40015481 Rev AAn increased number of complaints were reported on the Blood Pump Rotor (P/N - F40015481 REV A) after a period of use by clinics noting loose/dislodged guide sheaves.