Archive
556 recalls were announced in March 2024.
Of the 556 recalls this month scored against our rubric, 4% are Critical, 27% are Severe.
Which agencies issued them
Ford is recalling 2023-2024 Transit vehicles with the Trail package because tires may contact the wheel arch liner, risking tire damage and loss of control.
Suburban is recalling certain Slide-In Range models because the LED backlight circuit board may overheat, increasing the risk of a fire.
Ford is recalling certain 2024 Mustang vehicles with 2.3L engines because the low-pressure fuel supply line may be damaged or cut, which can result in a fuel leak.
Reading Truck Equipment is recalling 2021-2024 dump body trucks because inadequate clearance may allow the hood to contact the main electrical fuse terminal, increasing the risk of a fire.
Mercedes-Benz is recalling 2024 E350 and E450 vehicles because the transmission wiring harness may be routed too close to the driveshaft, potentially causing a loss of drive power.
Subaru is recalling certain 2020-2022 Outback and Legacy vehicles because an Occupant Detection System capacitor may crack and short circuit, preventing front passenger airbag deployment.
Twenty Four Six Foods LLC is recalling all flavors of Happiness USA Liquid Rolling Candy because the rolling ball applicator can dislodge into a child's mouth, posing a choking hazard and risk of death.
Nestlé USA recalls about 440,500 metallic mugs from 2023 holiday Starbucks gift sets sold at Target, Walmart, and military retailers. The mugs can overheat or break when microwaved or filled with extremely hot liquid, causing severe burns and cuts. 10 people have been injured in 12 reported incidents.
Kawasaki is recalling 1,579 motorcycles because damaged spark plugs can cause engine stalling, increasing crash risk.
Crown Boiler Company is recalling about 1,100 Crown Aruba IV (AWR Series) gas-fired hot water boilers due to a blocked vent switch that can fail to shut down burners at high altitudes, allowing carbon monoxide to accumulate in homes.
Jayco is recalling certain 2023-2024 Entegra and Jayco vehicles because the liquid level remote fill gauge on the propane tank may leak when in the "Open" position.
Ravin Crossbows LLC is recalling about 13,300 R500 series crossbows because they can unexpectedly discharge while being cocked or uncocked if not fully cocked, posing an injury hazard. The company has received one report of unexpected discharge but no injuries have been reported.
Culture Kings is recalling approximately 4,300 Sneaker Basel Magnetic Levitation Displays sold online from July 2020 through January 2023. The high-powered magnets can break and cause lacerations, or be swallowed and lodge in the digestive system, risking serious injury and death.
Fisher-Price is recalling Mickey and Friends figures sold since May 2023 because Donald and Daisy Duck heads can detach, posing a choking hazard. Three detachments were reported, including one found in a child's mouth, with no injuries.
BRS and BULin portable liquid fuel bottles sold on Amazon have non-child-resistant closures that violate federal safety law, posing risks of burns and poisoning to children. Consumers should stop using them and contact the seller for disposal and refund instructions.
BMW is recalling R1300 GS motorcycle side cases because latch hooks may fail, causing lids to detach and create road hazards.
Wheel Group Holdings is recalling AMP Terrain tires labeled as snow tires that lack sufficient traction for all snow conditions, increasing crash risk.
USDA FSIS issued a public health alert for frozen striped pangasius maws illegally imported from China. The products are ineligible for entry and unfit for human consumption.
Lamborghini is recalling 2024 Huracan vehicles because the high beam headlights may not activate, which can reduce visibility and increase crash risk.
CK Turkey and Cheese Sandwich is recalled for undeclared sesame allergen. The sandwich label lists only Wheat, Milk, and Soy allergens, missing sesame which poses risk to allergic consumers.
Prevost is recalling Eberspächer Hydronic L-II Heaters because they may generate excessive exhaust gas and overheat, posing risks of carbon monoxide poisoning and fire.
LiveWire is recalling certain 2024 S2 Del Mar motorcycles because the rear axle and lower shock joint nuts may not have been properly tightened. 165 units are affected.
Kia is recalling certain 2020-2024 Telluride vehicles because the intermediate shaft and right front driveshaft may not be fully engaged, which can result in roll away while in PARK.
Medos is recalling CERENOVUS CEREBASE DA Guide Sheaths due to reports of fractures at the distal end. Fractures may delay surgical procedures or cause vascular injury.
Trader Joe's Company is recalling Trader Joe's Southwest Salad (SKU 56077), 9 oz. due to potential Listeria monocytogenes contamination. Approximately 800,955 units were distributed nationwide.
Trader Joe's Company is recalling approximately 7,348 cases of Trader Joe's Elote Chopped Salad Kit nationwide due to potential Listeria monocytogenes contamination. All products with "Used By" dates on or before February 18, 2024 are affected.
Capitol Commissary LLC recalled 1,382 units of Jacksons Turkey and Cheese Sandwich due to undeclared sesame. The product was distributed across seven Western states and may pose a risk to consumers with sesame allergies.
Trader Joe's is recalling Cilantro Salad Dressing (SKU 36420) due to possible Listeria monocytogenes contamination. Approximately 15,890 cases were distributed nationwide.
A second Porsche recall covers certain 2020-2023 Taycan vehicles because the high-voltage battery may experience a short circuit within the battery modules. 606 units affected.
Porsche is recalling certain 2020-2024 Taycan vehicles because the high-voltage battery may experience a short circuit within the battery modules, increasing the risk of fire.
Prevost is recalling certain H3-45, H3-45 VIP and X3-45 coaches because the coolant heaters may generate excessive exhaust gas and overheat. 37 units are affected.
BrightFarms Southwest Chipotle Salad Kits are being recalled for potential Listeria monocytogenes contamination in the cotija cheese ingredient. Affected products have best-by dates from December 31, 2023 through February 22, 2024.
PACCAR is recalling certain Peterbilt and Kenworth trucks because improperly crimped gear shifter stalk connectors may cause a loss of communication. 70,509 units affected.
A hip prosthesis stem was recalled due to ambiguous carton label guidance that could cause incorrect implant selection during surgery. The recall affects 382 units.
Medline Industries is recalling CVS Health Waterproof Wound Tracking Dressing (REF CVS690330) due to sterility failure. The non-sterile dressings may introduce infection risk when applied to wounds.
The FDA is advising on label interpretation for the SPII Model Lubinus hip prosthesis stem to prevent confusion during surgery. Two complaints prompted additional guidance on carton label size and type columns.
Retractable Technologies is recalling EasyPoint Needles (25G x 5/8", REF: 82091) because the needle cannula may detach from the needle holder inside the patient.
FDA has recalled the D-Clip Standard/Mini Applier due to reports that the device failed to release the clip and remained attached during surgical use, creating a risk of surgical complications.
Siemens has recalled the Atellica IM Erythropoietin assay due to a 35% negative bias compared to WHO standards. The assay does not achieve claimed reference intervals and could report inaccurate test results.
Biosense Webster is recalling CARTO VIZIGO Bi-Directional Guiding Sheaths after inadvertently mixing unvalidated devices into production. The recall affects 853 units distributed nationwide.
Fresenius Kabi recalls Ivenix Infusion System software versions 5.2.1 and 5.2.2 due to two defects that may delay therapy or cause over-infusion. The software fix was deployed to affected units between May and August 2023.
Optikem International, Inc. is recalling TRP Natural Eyes Dryness Relief eye drops due to lack of assurance of sterility. The product was distributed nationwide in the USA.
Optikem International is recalling 46,621 bottles of hyalogic For Dry Eyes, HylaTears Lubricant Eye Drops due to lack of assurance of sterility. The product is distributed nationwide.
Capitol Commissary LLC is recalling 1,195 units of Jacksons Egg Salad sandwiches due to potential cross contact with sesame. Consumers with sesame allergies should not consume the affected product.
McKesson Medical-Surgical is recalling Rocuronium Bromide Injection vials due to storage outside label specifications. Seventy vials were distributed to three healthcare accounts in New Mexico, Arizona, and Utah.
Mckesson is recalling Bicillin L-A prefilled syringes stored outside label specifications. The FDA Class II recall affects 70 vials distributed to direct accounts in NM, AZ, and UT.
KALO Carrot Cake All Natural Gluten Free is mislabeled with Chocolate Cake ingredient information that omits soy, creating an allergen hazard for consumers with soy allergy.
The Perfect Bite Co. is recalling Mexican Street Corn Bites due to possible Listeria monocytogenes contamination. The product was distributed in California and Washington.
Capitol Commissary LLC is recalling CK Chicken Salad On A Croissant due to potential cross-contact with sesame. The recall affects 29 units distributed across seven Western states.
Capitol Commissary LLC is recalling Jacksons Chicken Salad On A Croissant due to potential sesame cross contact. The product was distributed in seven western states.
House of Coffee Beans, Inc is recalling coffee products distributed in Texas, South Carolina, and North Carolina due to potential cross-contact with almonds, pecans, and coconut. Consumers with allergies to these ingredients should not consume affected products.
Baxter Healthcare is recalling STERIS Boot Assembly traction devices due to an incorrectly oriented locking pin that may cause the boot to detach during surgery, posing patient safety risks.
The FDA is recalling 106,704 bottles of TRP Natural Eyes Red Eye Relief eye drops due to lack of sterility assurance. Consumers should stop using the product and contact a healthcare provider if they experience eye irritation or infection.
Baxter Healthcare recalls CLEARLINK Non-DEHP Solution Set Luer Lock Adapters due to potential leaks in the drip chamber. The recall affects 26,592 units distributed nationwide.
TRP Natural Eyes Pink Eye Relief sterile eye drops are being recalled due to lack of assurance of sterility. The recall affects 139,656 bottles distributed nationwide.
Vitony Bakery is recalling Bizcocho de Queso y Guayaba cheese-guava cake for undeclared FD&C Yellow #5 and Yellow #6 dyes. About 6,706 units were distributed in Puerto Rico.
KALO Chocolate Cake packages contain carrot cake with undeclared soy not listed on the label. Consumers with soy allergies are at risk of allergic reaction.
Sun Pharmaceutical is recalling 47,520 bottles of Febuxostat 40mg tablets nationwide due to microbial contamination found in manufacturing equipment. The FDA classified this as a Class II recall; no illnesses have been reported.
B. Braun Medical is recalling 22,752 bags of Potassium Chloride for Injection Concentrate nationwide due to pinholes in container bags that compromise sterility assurance. Affected lots are J2S007 (expires 12/31/2024) and J3A115 (expires 01/31/2025).
Eugia US LLC is recalling 1,160 vials of Tobramycin for Injection due to failed water determination testing. Affected lot numbers are 3TB23001 and 3TB23002, expiring 04/30/2025.
Peter Lazic GmbH's D-Clip Standard/Mini Applier is being recalled after a customer complaint that the device failed to release the clip during surgery, with the applier remaining attached to the clip.
Baxter Healthcare's Infuvite Adult Multiple Vitamins Injection is being recalled because 70 vials were stored outside their labeled specifications, potentially affecting product stability. The affected vials were distributed to three direct accounts in Arizona, New Mexico, and Utah.
Optikem International recalls TRP Eye Strain Relief eye drops nationwide due to lack of assurance of sterility. Affected units are 10 mL bottles with Lot E206.
TRP Natural Eyes Aging Eye Relief eye drops are being recalled because the manufacturer cannot assure the product meets sterility requirements. The recall affects 19,344 bottles distributed nationwide.
Optikem International is recalling TRP Natural Eyes Allergy Eyes Relief eye drops due to lack of assurance of sterility. The recall affects 30,240 bottles distributed nationwide.
Optikem International is recalling TRP Natural Eyes Floaters Relief eye drops nationwide due to lack of assurance of sterility in manufacturing. Affected bottles have lot numbers F404, F405, or F406.
Thea Pharma is recalling Betimol (timolol) ophthalmic solution nationwide for lack of sterility assurance and compromised container closure. The defects could allow contamination of the eye medication.
TRP Blur Relief sterile eye drops (Lot #B905) are recalled due to inability to assure product sterility. Approximately 7,248 bottles were distributed nationwide.
Micro Labs Limited is recalling 118,080 bottles of Telmisartan 40mg tablets due to failed blend uniformity specifications. The affected lots (SFBG024, SFBG025) were distributed in Puerto Rico, Tennessee, and Rhode Island.
TRP Eye Twitching Relief sterile eye drops are being recalled nationwide because the manufacturer cannot assure the product meets sterility requirements. The affected lot (C303, expiring 07-27-2025) was distributed in the USA.
A surgical clip applier from Peter Lazic Gmbh has been recalled after a reported failure to release the clip during surgery. The applier remained attached to the clip, potentially posing a safety risk during medical procedures.
Capitol Commissary LLC recalled CK Egg Salad Sandwich due to potential sesame cross-contact. Affected units were distributed in seven western U.S. states; consumers should not eat the product.
Shimadzu has recalled the Trinias Digital Angiography System due to a capacitor manufacturing issue that could cause abnormal display or system malfunction. No injuries have been reported.
Waldemar Link is recalling SPII Model Lubinus Long Stem Prosthesis XL Neck implants due to carton labeling that could be misinterpreted during surgery. Clearer guidance is being provided to prevent surgical misapplication.
Siemens Healthcare's ADVIA Centaur EPO Assay (lots 53984040, 55443042) produces readings 35% lower than the WHO standard, failing to achieve its claimed reference interval. No illnesses reported, but diagnostic inaccuracy poses risk of wrong clinical decisions.
Global Corporation is recalling Broncochem Cold & Tea nationwide due to stability testing failures in the active ingredients. No illnesses or injuries have been reported.
Electric City Sweets 1.75oz Red Velvet Milk Chocolate Bars are being recalled because milk is not properly declared on the packaging. The recall affects 1,644 bars distributed in California, Florida, Pennsylvania, and North Carolina.
Peter Lazic Gmbh is recalling 170 L-Aneurysm Clip TITANIUM Paddle-Clips distributed in Maine due to incorrect blue coloring instead of blank.
Global Corporation is recalling Broncochem Cold & Flu Syrup Kids (120 mL bottles) nationwide due to stability testing failures in active pharmaceutical ingredients.
Fresenius Kabi is recalling software versions 5.0.1 and earlier of the Ivenix Infusion System due to a software defect that may cause an incorrect pump alarm, potentially delaying therapy. The defect was resolved in software version 5.2.1, released in September 2022.
Vitony Bakery cheesecake products are being recalled due to undeclared FD&C Yellow #5 and Yellow #6 dyes. The recall affects 6,916 units distributed to Puerto Rico and may pose risks to consumers with sensitivities to these colorants.
Waldemar Link is clarifying labeling on 153 hip prosthesis units after complaints about ambiguous Size and Type information. The guidance aims to prevent potential misinterpretation during surgery.
Beaver Visitec International is recalling 3,000 BVI Visitec Irrigation Handles because the pack and pouch labels are missing manufacturing and expiration date information.
Sun Pharmaceutical is recalling 7,488 bottles of Febuxostat 80mg tablets nationwide due to microbial contamination found in manufacturing equipment. No illnesses have been reported.
Lidl US TRADING is recalling Banana Pepper Rings due to punctured lids on glass jars, which may compromise product integrity. Affected jars were distributed across multiple states in the Mid-Atlantic and Southeast regions.
Peter Lazic Gmbh is recalling 51 titanium aneurysm clip paddle clips because the clips are colored blue when they should be blank.
Jayco, Inc. is recalling certain 2023–2024 Jayco Solstice and Entegra Expanse motorhomes built on Ford chassis because the rearview camera may not display an image when in reverse, reducing rear visibility and increasing crash risk.
Chrysler is recalling certain 2024 Alfa Romeo Tonale vehicles because the manufacturer label is missing tire rim and tire size information, which could lead to incorrect wheel installation and increase crash risk.
Titan Bus is recalling 2018-2021 Chevrolet Express 3500 vehicles because the federal certification placard may be missing, which could lead to unintentional overloading and increased crash risk.
Cruiser RV is recalling 2023-2024 Avenir trailers because Federal Certification labels lack tire size and PSI data, potentially leading to incorrect tire installation or inflation.
Nova Bus is recalling certain 2021–2023 LFS buses because the alternator power cable nut may not have been tightened properly, increasing the risk of electrical arcing and fire.
Certain 2024 Genesis GV70 vehicles are recalled because water may leak into the transmission control harness, causing electrical shorts that shift the transmission from Park to Neutral, risking vehicle rollaway.
Mercedes-Benz is recalling specific 2019-2024 models because a 48-Volt ground connection may overheat, increasing the risk of a fire.
Dynamax Isata motorhomes (2023-2024) are recalled for a loose 12V disconnect nut that may cause electrical arcing and fire risk. Dealers will replace the part free of charge.
Airstream is recalling 2023 Basecamp 16 and 16X travel trailers because transposed weight labels may lead to unintentional overloading and increased crash risk.
Hyundai is recalling certain 2023 Ioniq 6 and related Genesis models because the 12-volt battery charger may fail, causing potential loss of drive power and increased crash risk. Repairs will be completed free of charge.
Chrysler is recalling 2023-2024 Jeep Wrangler, Ram, Pacifica, and other vehicles because a faulty steering column control module may prevent driver airbag deployment in a crash. Dealers will replace the module free of charge.
Certain 2018-2021 Chrysler 300 and Dodge Charger vehicles are being recalled for defective side curtain airbag inflators that may rupture. Dealers will replace both airbags free of charge.
Chrysler is recalling MOPAR steering column control modules used in 2017-2024 Jeep, Chrysler, and Ram vehicles because improper welding may prevent the driver's air bag from deploying.
Chrysler is recalling specific MOPAR side curtain air bag inflators sold as replacement parts for 2011-2020 vehicles due to a manufacturing defect that may cause rupture.
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