Archive
662 recalls were announced in March 2022.
Of the 662 recalls this month scored against our rubric, 4% are Critical, 25% are Severe.
Which agencies issued them
Meritor is recalling 180 Series Drive Pinions because they may fracture. A fractured pinion could engage the parking brake without warning, increasing crash risk.
Mack Trucks is recalling 2021-2023 LR Electric trucks because the power steering system may lose pressure, increasing crash risk.
Streamline Industries is recalling specific LA Chopper brake kits because the hydraulic brake hoses may lack required identification labels, potentially preventing future safety repairs.
Kia is recalling certain 2022 Sorento vehicles because the turbocharger oil supply pipe may crack, causing an oil leak that could increase the risk of engine fire.
Grand Design is recalling certain 2022 Reflection and Transcend travel trailers with 50-amp shore power inlets. The power inlet lug bolts may be too hard to tighten properly, creating loose electrical connections that can cause fire.
Heartland is recalling 2021-2022 North Trail trailers because the Gross Axle Weight Rating on the federal certification label is incorrect, risking vehicle overloading and crashes.
Bugatti is recalling one 2018 Chiron vehicle because a screw fastening the front frame support may be loose, potentially reducing structural protection in a crash.
Keystone is recalling certain 2022 Bullet, Outback, and Passport travel trailers due to improper welds on the coupler hitch. The defect can cause the trailer to separate from the tow vehicle, increasing crash and injury risk.
Mercedes-Benz is recalling 2022 S 500 and S 580 vehicles because a rear axle weld may be defective, posing a risk of loss of vehicle control.
Volkswagen is recalling certain Atlas and Atlas Cross Sport vehicles because corroded electrical contacts in the front door wiring harness may delay airbag deployment during side impacts, increasing the risk of injury.
Lance is recalling 2022 travel trailers because a data cable may rest on a burner box, increasing the risk of a fire. Dealers will reroute the cable free of charge.
Lance Camper is recalling 2022 models because a data cable may rest on the burner box, increasing the risk of a fire.
Hyundai is recalling 2019 Genesis G70 and 2020 Sonata models because a damaged trunk latch may prevent opening from the inside, risking entrapment.
Hyundai is recalling 2022 Santa Fe and Santa Cruz vehicles because the turbocharger oil supply pipe may crack, causing an oil leak that could increase fire risk in the engine compartment.
Ford is recalling 2021 F-150 vehicles because a software error may cause the transmission to unexpectedly shift into neutral, increasing crash risk.
Ford is recalling 2016 and 2020 Transit Connect vehicles because the front windshield may have inadequate adhesion to the body, increasing injury risk in a crash.
Mercedes-Benz is recalling certain 2021-2022 vehicles with heated leather steering wheels because a software error prevents the DISTRONIC hand-off detection system from functioning. This can disable warnings for drivers to grab the wheel and prevent emergency responder assistance.
Watson Hopper is recalling X12 Power Modules because fuel tubes may crack, causing a high-pressure fuel leak that increases fire risk.
Ford is recalling 2020-2022 Escape and 2021-2022 Bronco Sport with 1.5L engines. The oil separator housing may crack and leak, creating fire risk near hot engine components.
Ford is recalling 2022 Transit vehicles because the 360-degree camera system may fail to display the rearview image, increasing crash risk while reversing.
Miller Electric is recalling EnPak A60 units due to a bracket clearance issue that may cause electrical shorts, fuel leaks, or electrical arcs, increasing fire risk.
Mercedes-Benz is recalling 2022 EQS 450 and EQS 580 vehicles because a software error may permanently deactivate the overhead control panel, preventing occupants from contacting emergency services.
Forest River is recalling 2022 Surveyor travel trailers because a short fresh air intake tube may detach, causing the burn chamber to crack and expose occupants to carbon monoxide.
Ford is recalling 2022 Lincoln Aviator PHEV vehicles. The inlet charge port harness bus bar may unseat, causing loss of drive power and increasing crash risk.
Forest River is recalling 2022 Puma and Puma XLE fifth wheel and travel trailer recreational vehicles because the exterior microwave griddle can remain connected to propane when stowed, creating a fire hazard.
Ford is recalling 2022 Transit vehicles because the rearview camera may display a blank image when reversing, increasing crash risk.
Taylor Farms New England Inc. issued a public health alert for ready-to-eat chicken breast meal kits that may contain undeclared wheat and soy.
Ford is recalling 2022 F-150 and related models due to a software error that may disable trailer brake functionality. Loss of trailer brakes increases stopping distance and crash risk.
Boxine US is recalling tonies Blocks wooden toys containing high-powered magnets sold online from November through December 2021. When swallowed, multiple magnets can lodge in the digestive system and cause serious injury or death.
Prevost is recalling 140 X3-45 Commuter buses from 2021-2022 because a loose cable in the rear junction box may overheat and cause a fire.
EGL Motor is recalling about 500 EGL and ACE-branded youth ATVs (models MADIX 110 and B125) sold nationwide from May to September 2020 due to violations of federal ATV safety standards. The vehicles exceed speed limits for their age group, have defective brakes, and handlebars that pose laceration hazards in crashes.
Chrysler is recalling 2021-2022 Pacifica and 2021 Voyager vehicles because the second-row seat mounting latch may fail to secure the seat properly, increasing the risk of injury in a crash.
Commencal Ramones 14-inch children's bicycles lack required foot brakes and are equipped only with hand brakes, posing a crash hazard or risk of injury to young children unable to stop them. About 925 bicycles are affected.
Segway is recalling about 960 Ninebot children's bicycle helmets because they fail to meet safety standards for positional stability and retention, creating a risk of head injury in a crash. No injuries have been reported.
Sakar International is recalling about 89,000 Dimensions Bluetooth Speaker Helmets sold at Walmart because they do not meet U.S. federal safety standards for bicycle helmets and pose a risk of head injury in a fall.
Reading Truck is recalling 2019-2021 Master Mechanic Crane vehicles because a poorly mounted module can overheat and cause a fire.
Certain 2021-2022 Jeep Grand Cherokee L vehicles may have a missing weld in the child seat tether anchorage system. This could allow the tether to separate during a crash, increasing the risk of child injury.
Family Pharmacy of Statesville is recalling Trimix (Alprostadil/Papaverine/Phentolamine) injectable vials distributed in North Carolina due to lack of assurance of sterility.
Audi is recalling 2013-2017 A8, S6, S7, S8, and RS7 vehicles because a blocked turbocharger oil strainer can cause engine failure and increase crash risk.
Volkswagen is recalling certain 2022 and 2021 vehicles because rear suspension knuckles may corrode, crack, and break, potentially causing loss of stability and increasing crash risk.
Family Pharmacy of Statesville is recalling one lot of Fentanyl 150 mcg/mL Infusion Solution in 250 mL bags because the manufacturer cannot assure the product's sterility.
B. Braun Medical, Inc. is recalling 33,742 bags of 0.9% Sodium Chloride Injection USP due to leaking that compromises sterility assurance. The intravenous medication was distributed nationwide.
Jaguar Power Honey packaged in gold boxes is being recalled nationwide because it contains a hidden drug ingredient not listed on the label. Consumers should not consume this product.
SD Biosensor's STANDARD Q COVID-19 Ag Home Test kits were illegally imported without FDA approval, clearance, or authorization. Approximately 400,000 units were distributed nationwide.
Family Pharmacy of Statesville is recalling three bags of Ketamine 50 mg Infusion Solution because the manufacturer cannot assure sterility of the product.
Walmart is recalling Avaphinal Maximum Male Enhancement Sexual Pills (2000 MG, 10-capsule cartons, Lot DK1027) distributed nationwide because they contain undeclared sildenafil, making them an unapproved drug.
Family Pharmacy of Statesville is recalling Hydromorphone HCl 5 mg/mL Infusion in 250 mL bags because the manufacturer cannot assure the product meets sterility requirements.
Gourmet Kitchen, Inc. is recalling 43 boxes of Raw Buttermilk Breakfast Tarts due to undeclared almonds. Consumers allergic to almonds should not consume this product.
Family Pharmacy of Statesville is recalling Morphine Sulfate 6 mg/mL infusions in 250 mL bags due to lack of assurance of sterility. The affected product was distributed in North Carolina.
Ice cream products manufactured by Royal Ice Cream Company in Manchester, CT are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed across multiple states under various retail and food service brand names.
Family Pharmacy of Statesville is recalling Vancomycin 14 mg/mL Fortified Ophthalmic Solution due to lack of assurance of sterility. The affected lot was distributed in North Carolina.
Family Pharmacy of Statesville is recalling four bags of Hydromorphone HCl 1 mg/mL (250 mL each) distributed in North Carolina due to lack of assurance of sterility. The affected lots have beyond-use dates of October 25–30, 2020.
Family Pharmacy of Statesville is recalling Hydromorphone HCl 2 mg/mL Infusion 250 mL bags (2 units) distributed in North Carolina due to lack of assurance of sterility.
Family Pharmacy of Statesville is recalling one lot of Hydromorphone HCl 0.1 mg/mL Infusion in 1000 mL bags due to lack of assurance of sterility.
Family Pharmacy of Statesville is recalling Methylcobalamin 1 mg/mL Injectable in 1 mL syringes (Lot #07282020@3) distributed in North Carolina because the manufacturer cannot assure the product meets sterility standards.
Family Pharmacy of Statesville is recalling Lorazepam 1 mg/mL Infusion Solution in 250 mL bags because the manufacturer cannot assure sterility of the product.
Helmi Honey VIP is being recalled nationwide due to the presence of an undisclosed drug ingredient. Consumers should stop using the product and return it.
Gourmet Kitchen, Inc. is recalling 59 boxes of 14" Raw Buttermilk Breakfast Tart with Fresh Blueberries & Granola because they contain undeclared almonds, a tree nut allergen.
Albanese Confectionery is recalling specific lots of its Dark Chocolate Espresso Bean tubs due to undeclared peanut allergen. Consumers with peanut allergies who purchased this product should not consume it.
Boston Scientific is recalling RX CHOLANGIOGRAM KIT due to a sterile barrier breach that compromises device sterility. Approximately 500 units distributed worldwide are affected.
Stutzman Farms is recalling 4oz and 8oz bags of Sourdough Einkorn Pretzels due to undeclared wheat allergen. Consumers with wheat allergies should not consume this product.
Boston Scientific Corporation is recalling 1,811 units of Dreamtome Cannulating Sphincterotomes worldwide because the sterile barrier is compromised, creating a potential contamination risk.
Boston Scientific is recalling 142 units of DREAMTOME 44-30MM/450CM medical devices distributed worldwide due to a sterile barrier breach that compromises device sterility. Affected lot numbers are 27625066 and 27805561.
Hill-Rom Traverse Rail Carrier E-System components contain non-conforming screws that are too short to secure the rail properly. The screws could loosen over time, causing the rail system to fall and potentially injure caregivers or patients.
GE Healthcare is recalling 10,445 CARESCAPE Central Station monitoring systems. If connected to an unapproved keyboard, audio alarms may be muted, potentially preventing users from receiving critical notifications.
Boston Scientific is recalling 14 JAGTOME RX medical devices worldwide due to a sterile barrier breach that compromises the device's sterility.
Bard Peripheral Vascular Inc is recalling 1,260 Adult Lumbar Puncture Drug Free Trays due to manometer leaking and mating issues that could affect device function.
Boston Scientific is recalling 101 units of JAGTOME RX devices due to compromised sterile barriers that could allow contamination and infection. The recall affects devices distributed worldwide.
Stutzman Farms is recalling its organic einkorn berries due to undeclared wheat allergen. The recalled products were sold in bulk or in 25lb and 50lb bags across multiple states.
Boston Scientific is recalling 98 JAGTOME RX medical devices due to a sterile barrier breach. The affected units were distributed worldwide.
Port City Soups Alkaline Vegetable Soup (32oz glass jars) is recalled because its production process was not approved for acidified foods. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.
Stutzman Farms is recalling Organic Whole Einkorn Flour due to undeclared wheat allergen. The product poses a serious health risk to consumers with wheat allergies.
Fresh Creative Foods is recalling its Red Sauce Chicken Enchilada Kit due to plastic pieces discovered during manufacturing. The contamination came from ice supplied to the manufacturer.
Candies Tolteca is recalling Tolteca Saladitos Salted Dried Plums due to potential high lead contamination. Consumers should not consume affected product.
Bard Peripheral Vascular Inc. is recalling 2,880 Atraumatic Adult Lumbar Puncture Trays due to manometer leaking and mating failures. The devices were distributed nationwide and internationally.
Stutzman Farms is recalling Sprouted Einkorn Crackers sold in 0.30lb and 1lb bags due to undeclared wheat allergen. The affected product was distributed in Indiana, Kentucky, Michigan, Missouri, Ohio, Pennsylvania, and Wisconsin.
Boston Scientific is recalling 472 DREAMTOME stent devices due to sterile barrier breach affecting product sterility. Devices were distributed worldwide including the US.
Boston Scientific is recalling 254 units of the Hydratome RX 44-20MM medical device worldwide due to a compromised sterile barrier that may affect device sterility.
Boston Scientific is recalling 982 units of DREAMTOME medical devices due to sterile barrier breach that compromises device sterility. Affected units were distributed worldwide.
Bard Peripheral Vascular is recalling 116,770 adult lumbar puncture trays due to manometer leaks and connector mating defects that could affect procedure performance.
Bentley Motors is recalling certain 2020-2022 Continental GT and Flying Spur vehicles due to incorrectly installed front seat belt assemblies that may lack an automatic locking retractor, potentially failing to secure child restraints properly in a crash.
Fresh Creative Foods is recalling Thai Noodle Salad due to hard clear plastic pieces found during manufacturing. The contamination originated from ice supplied to the manufacturer.
Boston Scientific is recalling 21,309 units of the Dreamtome RX Cannulating Sphincterotome due to a sterile barrier breach that compromises device sterility, creating a potential infection risk to patients.
Boston Scientific is recalling 3,578 units of the JAGTOME RX medical device because the sterile barrier is compromised, which can allow contamination. The affected units were distributed worldwide.
Fresh Creative Foods is recalling Lemon Capellini Salad due to hard clear plastic pieces found in the product. The contamination source was traced to ice purchased from a supplier.
Fifteen Boston Scientific DREAMTOME medical devices are being recalled due to a sterile barrier breach that compromises device sterility. The affected lot number 27802363 requires appropriate action.
Bard Peripheral Vascular Inc. is recalling 2,880 Lumbar Puncture Drug Free Trays due to defects in the manometer component involving leaking and mating issues that could affect device function.
The ACUSON Juniper ultrasound system's clip storage function fails when the disk is full, potentially delaying treatment during critical imaging procedures. Healthcare facilities using this system should contact Siemens for support.
Alliance RV is recalling certain 2022 Valor, Paradigm, and Avenue travel trailers due to faulty power inlet bolts that can cause loose wiring and electrical fire risk. Dealers will replace the power inlet free of charge.
Boston Scientific is recalling 7,695 units of HYDRATOME RX devices worldwide due to compromised sterility from a sterile barrier breach. Affected devices may pose a risk of infection.
Bard Peripheral Vascular is recalling 49,760 SAFE-T PLUS lumbar puncture trays for adults due to manometer leaking and mating issues. Healthcare providers should discontinue use and contact the manufacturer.
Bard Peripheral Vascular is recalling 29,870 lumbar puncture trays due to manometer failure that causes leaking and improper connections. The defect could compromise device function during lumbar puncture procedures.
Bob Evan's Sour Cream & Chive Mashed Potatoes recalled due to incorrect packaging that failed to declare wheat allergen. Consumers with wheat allergies should not consume this product.
RMJV LP's First Street brand basil pesto sauce is recalled because hard plastic pieces were found in the product during manufacturing, traced to supplier ice.
Medtronic is recalling 8 LINQ II Insertable Cardiac Monitors due to moisture ingress susceptibility that may cause loss of functionality. Affected devices were distributed in the US (NJ, NY, PA, VA) and Italy.
Abbott Laboratories is recalling 306 units of Alinity s System software version 2.8.0 due to a software error causing insufficient wash buffer volume, which could affect diagnostic test accuracy.
Swanson Health Products is recalling Swanson Ultra Vitamin B12 Methylcobalamin supplements due to potential metal shavings in the product. The contamination poses a choking and injury risk.
Stutzman Farms is recalling Organic All Purpose Einkorn Flour sold in bulk due to undeclared wheat allergen. The product was distributed across seven Midwest states.
Fresh Creative Foods is recalling Thai Peanut Dressing due to the presence of hard plastic pieces potentially found in the product. The plastic originated from ice used during manufacturing.
Boston Scientific is recalling HYDRATOME RX 49-30MM/260CM devices worldwide because sterile barriers are compromised. The manufacturing defect affects device sterility.
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