Archive
600 recalls were announced in December 2023.
Of the 600 recalls this month scored against our rubric, 5% are Critical, 35% are Severe.
Which agencies issued them
Pierce is recalling 2019-2023 Arrow XT, Enforcer, and Velocity tower trucks because a wiring harness may not be secured, risking basket tipping and injury.
Wayne Farms is recalling approximately 1,377 pounds of ready-to-eat chicken breast products that may be undercooked. The recall was initiated after a customer complaint regarding product appearance.
Keystone RV is recalling 2021-2022 Dutchmen Coleman travel trailers with suspension springs rated at 4400 pounds instead of 5100 pounds. The underrated springs can become overloaded, increasing crash risk.
Volvo is recalling 2015-2024 XC90 vehicles because second-row seat belt buckle bolts may not be tightened properly, increasing injury risk in a crash.
Segway Powersports is recalling about 1,100 2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles because the ignition coil can fail, allowing fuel to enter the exhaust pipe and ignite, creating a fire hazard. One vehicle fire with property damage has been reported.
XpressGoods is recalling colorful neodymium magnetic balls that exceed federal safety limits for toy magnets. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.
Indian Motorcycle is recalling certain 2023-2024 models because an improperly routed sensor may cause the engine to stall, increasing crash risk.
Wet & Forget USA is recalling about 2.7 million bottles of "Xtreme Reach" Outdoor Mold & Mildew Stain Remover with hose end nozzles. The nozzle clip can dislodge, spraying cleaning solution on users and causing skin and eye irritation.
Security Equipment Corporation is recalling about 4,000 SABRE Aim & Fire Pepper Gel Spray canisters with expiration date 9/2027 because they lack a red nozzle needed to deploy the spray and will not function in an emergency. No injuries have been reported.
Ineos Automotive is recalling certain 2024 Grenadier vehicles with auxiliary switch package relays due to potential wiring damage that could cause electrical shorts and fire risk. Dealers will inspect and repair wiring at no cost.
Altec is recalling certain 2021-2023 aerial devices with Bobcat welders that may be misaligned, allowing fasteners to loosen and the welder to detach, becoming a road hazard and increasing crash risk.
Lamborghini is recalling 2015-2024 Huracán vehicles due to incorrectly adjusted headlights that fail to meet federal safety standards. The defect can reduce visibility of oncoming traffic and increase crash risk.
Pilotcar is recalling 2021-2023 PC-2, PC-4, and PC-6 electric vehicles because red rear reflectors may detach, reducing visibility and increasing crash risk.
Pilotcar is recalling 265 vehicles from 2021-2023 because the rearview camera and monitor were not installed, reducing rear visibility and increasing crash risk.
Adven Group LLC is recalling about 1,540 Nap Queen 12-inch Maxima Hybrid Mattresses sold via Amazon, Walmart, and Overstock because they fail to meet federal flammability standards and pose a fire hazard.
Mary Meyer is recalling about 1,950 Bubba Bull Plush Toys because the eyes can break off and pose a choking hazard to young children. No injuries have been reported.
Sumitomo is recalling specific Falken Wildpeak tires because a manufacturing error may cause sidewall punctures and air leaks, increasing crash risk.
Pilotcar is recalling 265 low-speed electric vehicles because they lack the required pedestrian warning sound system, increasing the risk of crashes.
The CPSC has recalled about 2,000 Vibe Bear playyard mattresses sold on Amazon.com from January to June 2023 due to suffocation hazard to infants. The mattresses violate federal crib mattress safety regulations and lack required warnings and labels.
USDA FSIS issued a public health alert for Whole Foods Market Kitchens soup mislabeled as beef, containing undeclared sesame.
Moonsea Pack and Play Mattresses sold on Amazon violate federal crib mattress safety regulations and pose a suffocation hazard to infants. Consumers should stop using them immediately and contact Moonseasleep for a refund.
Primark is recalling about 1,380 Wooden Music Shaker and DTR M&M Maracas baby rattles because the bottom portion can detach, creating a choking and ingestion hazard for children.
SourceOne Ventures recalls Windsor Queen Xtrabed Mobile Murphy Beds due to risks of cabinet breakage and tip-over. About 12,000 units sold at Wayfair between November 2016 and April 2023 are affected.
Volkswagen is recalling certain 2023-2024 ID.4 vehicles because the panoramic sunshade may not be fire retardant enough, violating federal safety standards.
Bunkhouse and Lotsa LITES! Connectable Mini String Lights can overheat and present burn and fire hazards when plugged directly into an outlet. About 34,600 units are affected.
The electric cord plug prong on Oreck Discover Upright Vacuums can detach and remain in electrical outlets, creating an electrical shock hazard. About 6,200 units sold nationwide from September 2022 through September 2023 are affected.
Bugaboo is recalling about 1,000 Dragonfly Seat Strollers because the backrest can move downward in parent-facing mode, causing unrestrained infants to potentially tumble from the seat. No U.S. injuries have been reported.
Ergodyne is recalling about 16,570 Squids 3705 Wire Tool Attachments because the wire can break when dropped while tethering a tool over two pounds, posing an injury risk to bystanders below.
Le Croissant Chicken Salad (5.8 oz, sold as Jack & Olive, Sprig & Sprout, or Food Unlimited) has been recalled due to undeclared milk and soy allergens. Approximately 4,146 units were distributed across 15 states and Washington D.C.
Garland Ventures is recalling 13,842 pounds of ready-to-eat chicken fried rice products that may be contaminated with Listeria monocytogenes.
Botanical Be is recalling Kuka Flex Forte caplets nationwide because they contain undeclared diclofenac and were marketed without required FDA approval. All lots expire 12/12/2024.
BMW is recalling certain 2023 models with a transmission control unit weld defect that may allow oil leakage, risking sudden power loss and increased crash risk.
Botanical Be is recalling 235 bottles of Artri King tablets sold nationwide. The tablets contain undeclared diclofenac and were marketed without FDA drug approval.
GreenGate Fresh Cello Spinach is being recalled due to potential E. coli (EHEC) contamination. The recall involves 11 cases distributed to eight consignees across seven U.S. states.
Eltahan Inc. is recalling Eltahan Golden Raisins (400g, UPC 2337660022) distributed in NY, NJ, and PA due to undeclared sulfites, which can cause severe allergic reactions.
Le Croissant Tuna Salad (5.8oz) is recalled due to undeclared milk and soy allergens. Consumers with allergies to these allergens should not consume the product.
Bayer Healthcare Pharmaceuticals Inc. is recalling 192 bottles of VITRAKVI (larotrectinib) oral solution due to microbial contamination identified as Penicillium brevicompactum during routine testing.
Reumo Flex caplets packaged in 30-count boxes are being recalled because they contain undeclared diclofenac and were marketed without FDA approval. The product was distributed nationwide.
Food Unlimited-brand Le Croissant Ham & Swiss sandwiches are being recalled due to undeclared milk and soy allergens. Affected products distributed across multiple states should not be consumed by people with these allergies.
BD Insyte Autoguard BC IV catheters may have needles that fail to retract properly, potentially causing contaminated needlestick injuries, blood leakage, and repeated insertion attempts.
Aizu Olympus gastrointestinal videoscopes (GIF-H190) may have defective repairs that prevent proper sterilization, risking patient exposure to contaminated material. Affected units were distributed to medical facilities in six states.
Kovatch Mobile Equipment is recalling 2020 Severe Service, Predator, and Spartan MetroStar trucks because a firmware defect may cause electrical fires.
Ferrara is recalling 2018-2020 Inferno Aerial Fire Apparatus trucks because a firmware defect may cause electrical circuits to overheat and increase the risk of fire.
Ducati is recalling 2016-2023 XDiavel S and STD motorcycles because the passenger backrest may break, increasing the risk of the passenger falling off.
Diet Coke 12oz aluminum cans sold in 12-pack fridge packs are being recalled due to potential foreign material. The recall affects 417 cases with specific lot numbers distributed to Alabama, Florida, and Mississippi.
Glenmark Pharmaceuticals is recalling Naproxen Sodium 250mg tablets nationwide due to a labeling mix-up where Indomethacin bottles may be labeled as Naproxen. Patients could receive the wrong medication.
24 Olympus EVIS EXERA III colonoscopes distributed to six states are recalled due to improperly repaired connectors that may cause image loss, decreased suction, or improper reprocessing, potentially exposing patients to contaminated equipment.
Siemens RAPIDPOINT 500e blood gas systems may show falsely elevated sodium readings in patients taking Perhexiline Maleate or Atomoxetine, risking misdiagnosis and inappropriate treatment of electrolyte imbalances.
Edwards Lifesciences is recalling 33,327 Acumen IQ Sensors used for intravascular pressure monitoring due to potential flushing difficulties during setup. The devices are distributed across the US and internationally.
PATH is recalling 28 units of SENTIERO Screening2 hearing examination devices due to potential technical distortions. The affected devices were distributed in Florida, Missouri, Ohio, and Wisconsin.
Aizu Olympus colonoscopes with improperly repaired light guide connectors may experience loss of image or suction failure. This could delay treatment and expose patients to contaminated material.
United Packers, LLC is recalling Sprite in 12-ounce aluminum cans distributed in Alabama, Florida, and Mississippi due to potential foreign material contamination.
Paroxetine tablets are being recalled for failing specification tests due to higher-than-acceptable levels of a degradation impurity. Approximately 1,941 bottles distributed nationwide are affected.
Abbott is recalling specific lots of the Alinity m HCV AMP Kit due to reports of false positive results and reactive negative controls. The kit detects hepatitis C virus in blood samples.
Aizu Olympus is recalling 24 colonoscopes with defective repairs to the light guide connector. The defect may prevent proper imaging, reduce suction, and impair device cleaning, potentially exposing patients to contamination.
Aizu Olympus recalls 24 gastrointestinal videoscopes with improperly repaired light guide connectors. The defect may cause loss of image and suction, preventing proper device reprocessing and risking patient infection.
Frito-Lay is recalling 16,100 bags of Chickpea Veggie Crisps (UPC 02840020646) due to undeclared milk allergen. Consumers with milk allergies should not consume the product.
Le Croissant Turkey & Cheddar sandwiches are being recalled due to undeclared milk and soy allergens. The product was distributed across 15 states.
Siemens RAPIDPOINT 500 Blood Gas System may produce falsely elevated sodium results due to drug interference from Perhexiline Maleate or Atomoxetine Hydrochloride. This could lead to missed hyponatremia or inappropriate treatment of hypernatremia.
Edwards Lifesciences is recalling 1417 FloTrac Sensors used for intravascular pressure monitoring due to potential flushing difficulties during kit setup. No illnesses or injuries have been reported.
California Bread Co. is recalling Telera Bread products due to undeclared milk allergen. The recall involves 8,959 packages distributed in California.
Food Unlimited Breakfast Sandwich Bacon Egg & Cheddar Croissants are recalled due to undeclared milk and soy allergens. The affected products have Use By dates from 10/27/2023 to 11/8/2023.
United Packers is recalling Fanta Orange in 12-pack aluminum cans due to potential foreign material. The affected product (Lot No. JUL2924MBD3) was distributed to Alabama, Florida, and Mississippi.
Bonta Natural Artisan Gelato Stracciatella is being recalled due to undeclared soy lecithin. Soy is a major allergen; consumers with soy allergies should not consume this product.
Apotex Corp. is recalling nationwide 25,776 units of Paroxetine Hydrochloride 30 mg tablets due to out-of-specification impurities. Affected lot numbers RV8686, RX0119, and RV2254 expire 08/2024.
Apotex Corp. is recalling Paroxetine 10 mg tablets nationwide due to out-of-specification impurities in an excipient. Affected lots expire 08/2024.
Glenmark Pharmaceuticals is recalling 37,200 bottles of Indomethacin 25mg capsules distributed nationwide because the bottles may be labeled as Naproxen instead. This labeling error could cause medication confusion.
Apotex Corp. is recalling Paroxetine Hydrochloride 40 mg tablets nationwide due to failed quality specifications. Testing found out-of-specification impurity levels in affected lot numbers.
Intuitive Surgical is recalling 317 units of a Da Vinci Single-Site Wristed Needle Driver due to potential dislodgement or breakage that could result in uncontrollable movement.
PATH's SENTIERO SCREENING hearing examination devices (Model SOH100098) are being recalled due to technical distortions that may exceed expected levels. The recall affects devices distributed in Florida, Missouri, Ohio, and Wisconsin.
Medtronic recalled 64,739 ICM LNQ22 LINQ II insertable cardiac monitors due to potential amplified noise or signal reduction that may interfere with heart rhythm recordings.
Breas Medical is recalling 215 mouthpiece units due to manufacturing defects with unintended slits that may result in insufficient ventilation in mechanical ventilation patients.
Edwards Lifesciences is recalling 168,014 TruWave with Vamp pressure monitoring kits due to potential flushing difficulties during setup. The recall affects devices distributed across the US and internationally.
PATH recalls SENTIERO hearing examination devices for excessive technical distortions. Affected units are distributed in FL, MO, OH, and WI.
Edwards Lifesciences is recalling 118,570 units of the TruWave Pressure Monitoring Set due to potential flushing difficulties during setup. The device is used for hemodynamic pressure monitoring.
EMD Millipore's Lugol's Iodine Solution (Lot 3124) is recalled due to an improper seal between the cap and bottle, which allows iodine vapors to dissipate and reduces the product's potency over time.
Bisousweet Confections is recalling certain Chocolate Whoopie Pie packages that contain Raspberry Whoopie Pies instead. Consumers should not consume the recalled products.
Edwards Lifesciences is recalling Acumen IQ intravascular pressure monitoring sensors (6,714 units) due to potential flushing difficulties during setup of the pressure monitoring kit.
Golden State Medical Supply Inc. is recalling Paroxetine 40 mg tablets due to failed impurity specifications. A total of 5,626 bottles were distributed nationwide.
VistaPharm LLC is recalling Aminocaproic Acid Oral Solution (0.25 grams/mL) distributed nationwide due to high ethylene glycol content from failed manufacturing specifications. Four lot numbers are affected.
Fagron Compounding Services is recalling 756 bottles of compounded ophthalmic medication because labels incorrectly identify the container as a 0.5mL single-use syringe instead of a 5mL dropper bottle. No adverse events have been reported.
Apotex Corp. is recalling Paroxetine Hydrochloride 20 mg tablets nationwide due to out-of-specification impurity levels in affected lots. No illnesses have been reported.
Teva Pharmaceuticals recalls specific lots of Testosterone Gel 1.62% for failing viscosity specifications. Patients should contact their healthcare provider to discuss the recall and obtain unaffected medication.
Edwards Lifesciences' FloTrac Sensor with Vamp System is being recalled due to potential flushing difficulties during setup of the pressure monitoring kit. No injuries have been reported.
Golden State Medical Supply is recalling certain lots of Paroxetine 20 mg tablets nationwide due to an out-of-specification chemical impurity in the product.
PATH is recalling AuDX PRO hearing examination devices because they may produce technical distortions greater than expected, which could affect diagnostic accuracy. The recall affects 23 units distributed in Florida, Missouri, Ohio, and Wisconsin.
Textron Specialized Vehicles is recalling 2024 Cushman Hauler Pro LSVs because water may enter the battery module, damaging circuits and increasing fire risk.
Terberg Benschop is recalling 2021-2022 YT193 terminal tractors because paint wear on the steering linkage may cause bolts to loosen or break, risking loss of steering control.
Certain 2024 Volvo VN and VHD trucks have an incorrect Gross Axle Weight Rating label, which can allow vehicles to be overloaded and increases crash risk. Dealers will replace the label free of charge.
Foiresoft Zebra Roller Blinds sold on Amazon.com have looped operating cords that pose a strangulation hazard to children. Consumers should stop using them immediately and contact Softfunch for a refund.
Eldorado is recalling 2019-2023 Axess and EZR buses because a transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.
Gillig is recalling 3,626 Low Floor vehicles from 2021-2023 because an incorrect fuse in the rearview mirror system may overheat and cause a fire.
Gillig is recalling 2023 Low Floor vehicles because inadequate lubricant in the rear axle hubs may cause axle failure, increasing the risk of a crash or injury.
Nissan is recalling certain 2023-2024 INFINITI QX60 vehicles because the Adaptive Front-Light System may incorrectly adjust headlights downward at high speeds, reducing visibility and increasing crash risk.
Porsche is recalling certain 2023-2024 718 models because the rear spoiler may raise too high, reducing brake light visibility and increasing crash risk.
Spartan Fire is recalling 69 fire apparatus units from 2020-2023 because a firmware defect may cause electrical circuits to overheat and start a fire.
Mercedes-Benz is recalling 2,797 2024 GLE 450e vehicles because a software error may increase the distance required to stop, raising crash risk.
Pelleh Poultry Corp. is recalling approximately 708 pounds of ready-to-eat beef and poultry products due to possible Listeria monocytogenes contamination.
Prevost is recalling 2022-2024 H3-45 VIP motorcoaches and 2024 H3-45 models because an incorrect bumper trim panel obstructs the radar sensor, preventing the driver assist system from functioning properly and increasing the risk of crashes.
Daimler Vans USA is recalling Freightliner and Mercedes-Benz Sprinter vans from 2021-2023 due to insufficient paint adhesion that may cause windows and interior lashing rails to detach during a crash. No injuries have been reported.
Looking for a different month? Back to 2023.