Archive
526 recalls were announced in June 2024.
Of the 526 recalls this month scored against our rubric, 3% are Critical, 25% are Severe.
Which agencies issued them
Global Homes USA is recalling about 400 Cedona Natural View six-drawer dressers sold at Rooms To Go for tip-over and entrapment hazards that can injure or kill children if not anchored to a wall.
CBOCS Distribution Inc. is recalling about 3,600 lavender scented candles in wooden bread bowls sold at Cracker Barrel Old Country Store from November 2023 through May 2024. The candle flames can reach excessive heights and ignite the wooden bowl, posing fire and burn risks.
Goal Zero is recalling about 34,460 Yeti Link Expansion Modules and EC8 Cables because the connections can overheat and melt, posing fire and burn hazards. Two reports of cables melting inside vehicles have been received with minor property damage but no injuries.
Babboe cargo bicycles manufactured by Babboe B.V. are being recalled because their frames can crack, bend, and break, posing a fall hazard to riders. The recall affects about 300 units sold in the United States through bicycle retailers nationwide between January 2011 and March 2024.
Toyota is recalling certain 2024 Grand Highlander and Lexus TX vehicles because the side curtain airbags may not unroll as intended and could partially deploy outside an open window.
Fisker is recalling all 2023-2024 Ocean vehicles because the exterior door handles can stick and fail to open, which can prevent occupants from exiting in an emergency.
Vitamix Ascent and Venturist Series 8-ounce and 20-ounce blending containers and blade bases can separate from their bases, exposing sharp blades. The company has received 27 reports of lacerations, including 11 from a previous 2018 recall.
Rivian is recalling certain 2022-2023 R1S and R1T vehicles because the maximum vehicle capacity weight value on the tire placard label is incorrect, failing FMVSS 110.
Newly Weds Foods is recalling its Breader X7 in 50-pound bags due to potential Salmonella contamination in an ingredient. The contamination poses a serious health risk.
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper contaminating the drug. The recall affects 2,806 vials distributed nationwide.
Grande Grande Primo Y45 cultured dairy product is being recalled due to possible Salmonella contamination. The product was distributed across multiple U.S. states and internationally to Canada, Ecuador, and Japan.
Grande Cheese Company is recalling Grande Bravo 600 Functional Whey Protein for possible Salmonella contamination. The affected product was distributed to 24 US states and to Canada, Ecuador, and Japan.
U.B.C. Food Distributors is recalling Baraka brand ground black pepper due to potential Salmonella contamination. The product is packaged in 7oz retail containers with UPC 8 22514 26626 6.
Kerry, Inc is recalling Scallop Pot Seas frozen scallop ingredient due to potential Salmonella contamination. The product was distributed to commercial customers in multiple U.S. states and Canada.
Grande Bravo 550 Functional Whey Protein is being recalled due to possible Salmonella contamination. Affected batches ANV508-1 and ANV508-3 were distributed across 24 U.S. states and internationally.
Kerry Inc. is recalling 77 bags of Cheddar & Sour Cream SEAS seasoning (lots 8092105, 8127605, 8091886) distributed across multiple U.S. states and Canada due to potential Salmonella contamination.
Grande Bravo 500 Functional Whey Protein is recalled due to possible Salmonella contamination. The product was distributed across 24 US states and internationally to Canada, Ecuador, and Japan.
Irvington Seafood is recalling claw crab meat due to Listeria monocytogenes contamination found during product testing. The affected product was distributed in Mississippi and Alabama.
Grande Cheese Company is recalling Grande Bravo 300 Functional Whey Protein (SKU 32102) due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.
Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.
Grande Lactose (SKU 30601) is being recalled due to possible Salmonella contamination. The affected product was distributed across multiple US states and internationally.
Newly Weds Foods, Inc. is recalling Starch WPC Blend 30lb bags due to potential Salmonella contamination in the ingredient. The recall affects 4,020 pounds of product distributed in Florida, Illinois, and Texas with lot numbers MT712282 and MT712283.
Grande Ultra 9150 Whey Protein Isolate (Product Code 32324) is being recalled due to possible Salmonella contamination. The affected product was distributed to 24 US states and internationally to Canada, Ecuador, and Japan.
Irvington Seafood, Inc. is recalling Lump Crab Meat due to Listeria monocytogenes contamination identified in finished product testing. The recalled product was distributed in Mississippi and Alabama.
Irvington Seafood is recalling Jumbo Crab Meat due to Listeria monocytogenes found during product testing. Affected packages distributed in Mississippi and Alabama should not be consumed.
Newly Weds Foods, Inc. is recalling 50-pound bags of breader (lot CD032324M) due to potential Salmonella contamination in an ingredient. The product was distributed to customers in Florida, Illinois, and Texas.
Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.
H & U Inc. dba Sun Noodle is recalling S&S Cup Saimin-Noodles because the product contains undeclared egg, a major allergen. Approximately 39,522 cases were distributed in Hawaii, California, Nevada, and Utah.
GRANDE CHEESE COMPANY is recalling Grande Ultra 9100 Functional Whey Protein Isolate (SKU 32131) due to possible Salmonella contamination. The recall affects 1.7 million pounds distributed to 24 U.S. states and international markets.
Irvington Seafood is recalling Finger Crab Meat due to Listeria monocytogenes contamination identified during product testing. The recall affects 168 lbs distributed in Mississippi and Alabama.
Kerry Ingredients is recalling 13,341 bags of Sun Nat HV CHDR #3 SEAS food ingredient due to potential Salmonella contamination. No illnesses have been reported.
Grande Cheese Company is recalling Grande Bravo 250 Functional Whey Protein (SKU 32101) for possible Salmonella contamination. The recall affects 1,726,910 pounds distributed across 24 U.S. states and exported to Canada, Ecuador, and Japan.
Grande Cheese Company is recalling Grande Ultra 8000 Nutritional Whey Protein Isolate due to possible Salmonella contamination. The affected batches include AOE813-1 through AOE813-4 and AOF840-1 through AOF840-4.
Kerry, Inc is recalling BrS8 RODIZIO Seas No MSG seasoning ingredient due to potential Salmonella contamination. The affected product was distributed to multiple U.S. states and Canada.
Kerry, Inc has recalled Salt & Vinegar seasoning product due to potential Salmonella contamination. The affected product was distributed in multiple U.S. states and Canada.
Newly Weds Foods is recalling G51904 Steak and Burger Seasoning due to potential Salmonella contamination in an ingredient. Approximately 4,685 pounds were distributed to Florida, Illinois, and Texas.
Integra LifeSciences is recalling CODMAN BACTISEAL EVD catheters due to external packaging seal defects that may compromise sterility. The recall affects 59 units distributed internationally.
Rygel Advanced Machines recalls OMTech Desktop Laser Engravers due to missing safety interlocks and labeling. The devices lack required redundant interlocks and certification labels that prevent accidental laser exposure.
Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.
Tesla is recalling certain 2024 Cybertruck vehicles due to excessive electrical current that can cause the front windshield wiper motor controller to fail, reducing visibility and increasing crash risk.
Imprimis NJOF, LLC is recalling one lot of a compounded ophthalmic suspension due to failure of sterility assurance. The product may be contaminated and pose a risk of serious eye infection.
Porsche is recalling certain 2020–2025 Taycan vehicles because the front brake hoses can develop cracks and leak brake fluid, reducing braking performance. Dealers will replace the hoses for free.
Wondfo USA has recalled 170,000 units of Clarity Strep A Rapid Test kits due to unauthorized distribution for at-home use, non-prescription use, over-the-counter use, and direct-to-consumer sales. The recall affects test kits distributed nationwide.
RemedyRepack Inc. is recalling bottles labeled as Phenazopyridine HCl 100mg that actually contain Phenobarbital 16.2mg tablets. Eight bottles were distributed to one medical facility. Patients should not use these medications and must contact their healthcare provider.
B Braun Medical Inc is recalling 108,811 units of Stimuplex A anesthesia needles because the devices are labeled as DEHP-free but the glue contains traces of DEHP.
Integra LifeSciences recalls CODMAN EVD BACTISEAL catheters due to defects in sterile packaging that may compromise product sterility. The defect affects 106 units distributed worldwide.
Wondfo USA is recalling 102,500 units of IMCO Strep A Rapid Test Kits due to unauthorized distribution for at-home, over-the-counter, and direct-to-consumer use.
Fresenius is recalling 4 hemodialysis water purification devices for pressure control malfunctions. When concentrate pressure exceeds the 19.9 bar limit, the device stops supplying water and halts dialysis treatment.
Wondfo USA has recalled Streptococcal A rapid test kits that are being sold for unauthorized at-home and direct-to-consumer use. The kits should not be used outside professional healthcare settings.
Canon Medical MRI systems are being recalled because the terminal block securing the power cable may disconnect, potentially causing electrical arcing and fire. 153 units are affected across the United States and Puerto Rico.
Coviden Monoject 60ml Luer-Lock syringes were inadvertently distributed despite being quarantined. Mckesson Medical-Surgical is recalling approximately 100 units (lot 330737X) distributed in the United States.
Covidien is recalling EsoFLIP 30mm balloon dilation catheters due to saline conductivity issues that may cause inaccurate esophageal measurements, potentially leading to patient harm.
B Braun Medical Inc is recalling Stimuplex A injection needles because the devices are labeled as DEHP-free, but the glue used contains traces of DEHP. The recall affects 20,850 units distributed in the US and Canada.
Imprimis is recalling Klarity-C, a cyclosporine eye medication, because the company cannot assure the product meets sterility standards. Approximately 136,005 units were distributed nationwide.
Pacira Pharmaceuticals is recalling 43,768 kits of Zilretta injectable suspension due to failed stability specifications at 2–8°C storage for 12 months followed by 25°C for 6 weeks. No illnesses or injuries have been reported.
Winder Laboratories is recalling Phenazopyridine HCl tablets (Lot #1142404) due to a product mix-up where some bottles contain Phenobarbital tablets instead. No illnesses or injuries have been reported.
Grande Cheese Company is recalling Grande Lactose SKU 30600 due to possible Salmonella contamination across 24 U.S. states and three countries. No illnesses have been reported.
Jamai Bou CHADNI HOT MIX CHANACHUR snack is being recalled because peanuts are present but not declared on the label. This poses a serious risk to consumers with peanut allergies.
Integra LifeSciences is recalling 135 CODMAN BACTISEAL EVD Catheter Sets due to defects in sterile packaging that may compromise product sterility.
GE Medical Systems is recalling MyoSPECT cardiac imaging systems due to service handles on internal lead covers that could loosen or release, potentially causing the cover to drop and injure service personnel. The recall affects 133 devices distributed worldwide.
The CORI Starter Kit surgical system may experience display flickering from a software tracking error, potentially causing surgical delays during orthopedic procedures.
Ortho-Clinical Diagnostics is recalling VITROS Anti HBs Calibrators due to potential for positively biased results caused by signal reduction over shelf life. Approximately 481 units were distributed worldwide.
B Braun Medical Inc is recalling over 1.1 million Stimuplex A nerve block needles labeled as DEHP-free, but the adhesive contains traces of DEHP. The mislabeling poses a risk to users who selected the product specifically to avoid DEHP exposure.
Stimuplex A nerve block needles labeled as DEHP-free contain trace amounts of DEHP in the adhesive. B Braun is recalling approximately 1.78 million units distributed in the US and Canada.
Avanos Medical is recalling NEOMED oral syringes because expiration dates were not printed on outer shipping labels, allowing expired units to reach customers.
Tesla is recalling certain 2024 Cybertruck vehicles because the trunk bed trim sail applique may be improperly adhered and can loosen or detach, creating a road hazard.
Organon LLC has voluntarily recalled 2,886 units of Asmanex inhalation powder nationwide due to defective containers.
Avanos Medical recalls NEOMED nonsterile pharmacy syringes because expiration dates were not printed on outer shipping labels, resulting in expired products being distributed.
Avanos Medical is recalling NEOMED Pharmacy Syringes because expiration dates were not printed on the outer shipping labels. Approximately 37,476 cases of various syringe sizes were distributed worldwide.
Wondfo USA recalls Areta Strep A test kits (Lot E03920802) distributed for unauthorized at-home and over-the-counter use. The recall affects 75,000 units distributed nationwide.
Organon LLC is recalling Asmanex Twisthaler (mometasone furoate) inhalation powder nationwide due to defective containers. Affected lot #Y000085 expires April 25, 2025.
Organon LLC is recalling 2,551 units of ASMANEX Twisthaler mometasone furoate inhalation powder nationwide due to defective containers. Affected lot X024051 expires April 25, 2025.
Wondfo USA is recalling approximately 1.2 million Preview Strep A rapid test kits (Part Numbers PRE-STA-25 and PRE-STA-A-10) that were distributed for at-home and direct-to-consumer use. The device is intended for professional channels only.
Young Dental Manufacturing is recalling 534 units of Darby Prophylaxis Paste with 1.23% Fluoride Ion (Lot 248607) due to incorrect part number labeling. The product was labeled as part number 045032 instead of the correct 040032.
Waco Bottling LLC is recalling TriyBrewed Coffee Concentrate 6oz bottles due to missing ingredient statement and nutrition label. Consumers cannot verify product contents or nutritional information.
Spartan Fire is recalling 2017-2019 Gladiator and 2018-2019 Metro Star fire trucks because service brakes may engage slowly, increasing crash risk.
Southeast Toyota Distributors is recalling 2021–2024 Toyota Highlander vehicles due to 20-inch accessory tires with insufficient load ratings. Overloaded tires can fail and increase crash risk.
Entrans is recalling 2017 Polar Tank ARJH trailers because improper tank welding may cause leaks, creating a road hazard and increasing crash risk.
Ford is recalling 2014 F-150 vehicles because a signal loss can cause unexpected downshifting into first gear, increasing crash risk.
Micro Bird is recalling 2011-2025 G5 school buses because certain seats may be improperly attached, increasing injury risk in a crash.
Nova Bus is recalling 2021 LFS buses because welds may fail, allowing the door to open while in motion and increasing injury risk.
Jaguar Land Rover is recalling certain 2023–2024 Defender and 2024 Discovery, Range Rover, Range Rover Sport, and Range Rover Velar vehicles because the oil filter housing can crack and leak oil into the engine compartment, increasing the risk of fire.
Mack Trucks is recalling 2024 MD Electric vehicles because a high voltage connector may not lock properly, risking sudden loss of steering and drive power.
Mercedes-Benz is recalling 2022-2023 C 300 vehicles because an improperly tightened bolt on the pre-fuse box wire could cause overheating, leading to fire or loss of drive power.
Ford is recalling 2021 F-150 trucks with Onboard Scales because a software update may have disabled the reverse lights, increasing crash risk.
Thor Motor Coach is recalling 2023-2024 Magnitude and Omni motorcoaches because the emergency exit window can become blocked when the outside griddle is in use, potentially delaying evacuation during an emergency.
Mercedes-Benz USA is recalling certain 2019-2025 CLS 53, E 53, GT 43, and GT 53 models due to transmission wiring harness defects that may cause corrosion and electrical short-circuits, increasing fire risk. Dealers will replace the harness free of charge.
Ford is recalling 2023-2024 Escape vehicles with adaptive cruise control due to misaligned radar modules. The misalignment can cause unexpected braking and loss of safety system function, increasing crash risk.
Toyota is recalling certain 2023 Crown vehicles with defective rearview and frontview cameras that may separate and allow water infiltration, potentially failing to display images and reducing driver visibility.
About 2,600 magnetic chess games with 20 magnet pieces sold on Temu.com from December 2023 through February 2024 are recalled because the magnets violate federal toy magnet regulations and pose a serious ingestion hazard.
Southern Telecom is recalling about 19,500 Lomi Roll-On Waxing Kits because the power cord can overheat and short circuit, creating fire, burn, and electrical shock hazards. Two consumers suffered burns and one incident of property damage has been reported.
Adven Group is recalling approximately 117,200 Nap Queen Sleep Victoria Hybrid Mattresses sold nationwide from February 2020 through October 2023 because they violate federal flammability regulations, posing a fire hazard.
Airstream is recalling 2024 Interstate motorhomes because a missing 12-volt fuse could allow the supply wire to overheat, increasing the risk of fire.
Altec is recalling 2023-2024 aerial devices and related truck-mounted equipment due to lighting wire harness overload that may prevent vehicle lights from illuminating, reducing visibility to other drivers and increasing the risk of crashes.
Jayco is recalling 2024 Jay Feather travel trailers because a 14-inch spare tire was installed with a 15-inch tire placard, creating a risk of incorrect inflation and crashes.
Certain 2021-2023 Chrysler, Jeep, Ram, and Dodge vehicles have defective radio software that may prevent the rearview camera from displaying, reducing driver visibility when backing up.
Chrysler is recalling one 2022 Ram 1500 Classic because a wiring harness short may prevent the rearview camera from displaying, increasing crash risk.
Terex is recalling 2022-2023 TM-Series vehicles because the master leveling controller may lose the ability to level the platform if power is lost while squeezing the enable trigger.
Certain 2023 Jeep Grand Cherokee vehicles have a loose second-row seat belt buckle bolt that may not properly restrain occupants during a crash. Dealers will inspect and tighten the bolt free of charge.
Looking for a different month? Back to 2024.