The Recall Desk

Archive

March 2023 recalls

1,013 recalls were announced in March 2023.

What the numbers show

Critical
68
Severe
432
High
400
Moderate
107
Low
6

Of the 1,013 recalls this month scored against our rubric, 7% are Critical, 43% are Severe.

1–100 of 1013

  • SevereNHTSA·23V227000·2023-03-31

    Forest River Recalls 2023 East to West Travel Trailers Due to Drawbar Defect

    Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because the drawbar assembly may break, potentially allowing the trailer to detach.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V235000·2023-03-31

    Tesla Recalls 2018-2019 Model 3 Vehicles for Suspension Fastener Issue

    Tesla is recalling 2018-2019 Model 3 vehicles because front suspension fasteners may loosen, potentially causing the lateral link to separate and increasing crash risk.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E027000·2023-03-31

    Lippert Recalls WAY Solar Panels With Insufficient Installation Hardware

    Lippert is recalling WAY Solar Panels because mounting hardware may become loose and pull through the panel slot, potentially causing the panels to detach from the vehicle during transit.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V233000·2023-03-31

    2022 and 2023 Rivian R1S Reverse Lights May Have Reduced Visibility

    Rivian is recalling certain 2022 and 2023 R1S vehicles because the reverse light beam may not be visible from certain angles, increasing the risk of a crash.

    Product
    RIVIAN — RIVIAN R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E028000·2023-03-31

    Felling Trailers Recall Warn Winch Remotes Due to Water Intrusion Risk

    Felling Trailers is recalling 2022-2023 trailers equipped with Warn winches because water may enter the remote control, causing corrosion and unintentional winch operation.

    Product
    FELLING — FELLING DECK-OVER, DROP-DECK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V226000·2023-03-31

    2023 Forest River Cherokee Travel Trailers Safety Chain Recall

    Forest River is recalling certain 2023 Cherokee CKT36FBOP Travel Trailers because the safety chains may be insufficient for the Gross Vehicle Weight Rating listed on the federal placard, allowing the trailer to detach and increase crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V234000·2023-03-31

    2021–2023 Winnebago Ekko motorhomes recalled for electrical fire risk

    Winnebago is recalling certain 2021–2023 Ekko motorhomes due to improperly routed wires and loose electrical connections in the 12-volt charging system that can cause fires.

    Product
    WINNEBAGO — WINNEBAGO EKKO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V231000·2023-03-31

    Gulf Stream Recalls 2023-2024 Conquest and BT Cruiser Motor Homes

    Gulf Stream is recalling 2023-2024 Conquest and BT Cruiser motor homes because the entry door latch may fail, preventing entry or exit.

    Product
    GULF STREAM — GULF STREAM CONQUEST, BT CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V232000·2023-03-31

    Mercedes-Benz Recalls 2023 AMG CLA 45 Vehicles for Tire Air Leaks

    Mercedes-Benz is recalling 2023 AMG CLA 45 vehicles because tires may leak air, which could cause a loss of vehicle control and increase the risk of a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG CLA45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V236000·2023-03-31

    2022 and 2023 Kia Carnival power sliding doors auto-reverse failure

    Kia is recalling 2022 and certain 2023 Carnival vehicles because the power sliding doors' auto-reverse feature may not activate in all situations, risking occupant injury.

    Product
    KIA — KIA CARNIVAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23172·2023-03-31

    The Laundress Fabric Conditioners Recalled for Ethylene Oxide Contamination

    The Laundress is recalling about 800,000 fabric conditioner products sold nationwide from 2011 through November 2022 because they may contain ethylene oxide, a chemical carcinogen. Consumers should stop using the products immediately and contact The Laundress for a refund.

    Product
    The Laundress Fabric Conditioners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·23165·2023-03-30

    Jetson Rogue 42-Volt Self-Balancing Scooters Recalled for Fire Hazard

    Jetson Electric Bikes is recalling about 53,000 Jetson Rogue 42-volt self-balancing scooters due to overheating lithium-ion batteries that pose a fire hazard. Two deaths have been reported.

    Product
    42-volt Jetson Rogue self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V228000·2023-03-30

    Honda Recalls 2007-2011 CR-V Vehicles for Frame Corrosion Risk

    Honda is recalling 2007-2011 CR-V vehicles sold or registered in specific states due to frame corrosion that could cause the rear trailing arm to detach.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23166·2023-03-30

    Higdon Outdoors Waterfowl Decoy Battery Packs Recalled for Fire Hazard

    Lithium-ion battery packs in Higdon Outdoors XS Series waterfowl decoys can overheat and catch fire while charging. The manufacturer received 20 overheating reports including 9 fires, 7 with property damage, though no injuries have been reported.

    Product
    Battery packs and replacement batteries on XS Series Pulsators, Swimmers, Crazy Kicker, and Flasher motion decoys used for waterfowl hunting
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V229000·2023-03-30

    Honda Recalls 2023 Civic Type R for Driver Seat Frame Welding Defect

    Honda is recalling 2023 Civic Type R vehicles because the driver's seat frame may not be welded properly, which could cause the seat cushion frame to break and increase injury risk in a crash.

    Product
    HONDA — HONDA CIVIC TYPE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V217000·2023-03-30

    Jayco and Entegra motorhomes recalled for rear stabilizer bar brackets

    Jayco and Entegra motorhomes from model years 2021–2022 have rear stabilizer bar attachment brackets that may break and separate from the vehicle, creating a road hazard and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO VISION XL, EMBLEM, ALANTE, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23169·2023-03-30

    Cannondale Tesoro Neo X Speed Electric Bicycles Recalled for Fall Hazards

    Cannondale is recalling about 75 Tesoro Neo X Speed electric bicycles because the hand brakes are configured to the European standard, which is reversed from the U.S. standard, creating a fall and injury hazard to riders.

    Product
    Cannondale Tesoro Neo X Speed Electric Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V220000·2023-03-30

    International LT and RH Trucks Engine Control Module Software Issue

    Navistar is recalling 2021–2024 International LT and RH trucks because the engine control module may become unresponsive to throttle pedal input, causing the vehicle to unexpectedly slow to idle speed while driving, which increases crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V216000·2023-03-30

    Altec Recalls Digger Derricks and Aerial Devices Due to Missing Weld

    Altec is recalling 2016-2022 digger derricks and aerial devices because a missing weld on the rear pole rack could cause the pole to drop, increasing injury risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V221000·2023-03-30

    2019–2022 Land Rover Range Rover PHEV vehicles engine cooling system fire risk recall

    Jaguar Land Rover is recalling 2019–2022 Range Rover PHEV and Range Rover Sport PHEV vehicles because a damaged drive belt can cause engine overheating, coolant leaks, and fire risk in the engine compartment.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT PHEV, RANGE ROVER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23167·2023-03-30

    Solexio STYLR Hair Stylers Recalled for Electrocution Hazard

    Solexio STYLR Hair Stylers are being recalled because the power cord can detach if the unit is dropped, creating an electrocution or shock hazard. Consumers should stop using the product immediately and contact the company for a refund.

    Product
    STYLR Hair Stylers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V223000·2023-03-30

    Four Degree Recalls 2019-2022 Trailers Due to Winch Remote Water Intrusion

    Four Degree is recalling 2019-2022 Lo-LAL and IPT-EOT trailers because water can enter the winch remote, causing corrosion that allows the winch to operate unintentionally.

    Product
    FOUR DEGREE — FOUR DEGREE IPT-EOT, LO-LAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23170·2023-03-30

    Delta Enterprise 2-in-1 Outdoor Kids Swings Recalled for Fall Hazard

    Delta Enterprise Corp. is recalling approximately 43,380 2-in-1 Outdoor Kids Swings because the seat restraint straps can break, creating a fall hazard for young children. No injuries have been reported.

    Product
    2-in-1 Outdoor Kids Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V224000·2023-03-30

    2022–2024 Jayco and Entegra motorhomes recalled for software error

    Jayco and Entegra motorhomes (2022–2024 models) may lose drive power or key safety functions due to a vehicle control module software error, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO CORNERSTONE, ASPIRE, REATTA, EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23741·2023-03-30

    JBM International Adult Bike Helmets Recalled for Head Injury Risk

    JBM International is recalling about 5,300 adult bike helmets sold on Amazon.com from March 2022 through January 2023 because they do not meet federal safety standards and can fail to protect the head in a crash.

    Product
    Adult Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V222000·2023-03-30

    2023 Land Rover Range Rover engine oil drain pipe gasket recall

    Jaguar Land Rover is recalling one 2023 Range Rover because a turbo oil drain pipe gasket may be incorrectly installed or missing, risking an oil leak and potential fire.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23740·2023-03-30

    Polaris RZR Pro R and Pro R 4 vehicles recalled for fire hazard

    Polaris is recalling about 200 Model Years 2022-2023 RZR Pro R and Pro R 4 recreational off-road vehicles because the alternator can fail during operation and pose a fire hazard. The company has received four reports of alternator failure, including two fire incidents, with no injuries reported.

    Product
    Model Years 2022-2023 RZR Pro R and Pro R 4 Recreational Off-Road Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23168·2023-03-30

    Open Cycle Bicycles Recalled Due to Rear Brake Failure Hazard

    Open Cycle UP Ekar, UPPER Ekar, WIDE Ekar, and MIND Ekar bicycles with Campagnolo hydraulic rear disc brakes are being recalled because the rear brake can fail, posing a crash hazard. About 270 units sold nationwide from November 2021 through February 2023 are affected.

    Product
    Open Cycle UP Ekar, UPPER Ekar, WIDE Ekar and MIND Ekar bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23171·2023-03-30

    Carhartt Men's Work Pants Recalled for Fall Hazard from Hem Loop

    Carhartt Men's Force Relaxed 5 Pocket Work Pants can develop an extended elastic loop at the ankle that poses a trip and fall hazard. About 32,505 units sold at Dick's Sporting Goods from July through November 2022 are affected.

    Product
    Carhartt Men's Force Relaxed 5 Pocket Work Pants
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0635-2023·2023-03-29

    YAMANAKAFOODS Salted Hijiki Seaweed 20g Recalled for Undeclared Wheat Allergen

    YAMANAKAFOODS Seasoning - Salted Hijiki Seaweed (20g) is being recalled because the label does not disclose wheat as an ingredient. Consumers with wheat allergies are at risk of allergic reaction.

    Product
    YAMANAKAFOODS Seasoning - Salted Hijiki Seaweed 20g UPC: 4902378014053 Made in Japan
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-0632-2023·2023-03-29

    IWATSUKASEIKA Soybean Flavor Snack Recalled for Undeclared Wheat Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling IWATSUKASEIKA Soybean Flavor snacks because wheat was not declared on the label. Consumers with wheat allergies should not consume this product.

    Product
    IWATSUKASEIKA Soybean flavor 72g -21pieces UPC: 4901037131919 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0633-2023·2023-03-29

    Powdered lemon tea recalled for undeclared milk allergen

    MEITO An extra Stick Powdered Lemon Tea is recalled because the product contains milk that is not declared on the label. Consumers with milk allergies who have purchased this product should not consume it.

    Product
    MEITO An extra Stick Powdered Lemon Tea 5packs UPC: 4902757442804 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0488-2023·2023-03-29

    Delsam Pharma Artificial Eye Ointment Recalled for Bacterial Contamination

    Delsam Pharma's Artificial Eye Ointment is being recalled for bacterial contamination in unopened tubes. FDA analysis found non-sterility defects in approximately 50,000 units.

    Product
    Delsam Pharma's Artificial Eye Ointment (Mineral Oil 15%, White Petrolatum 83%), 3.5 grams (1/8 oz.) tube, Distributed By: Delsam Pharma Lic, Bronx, Newyork 10469, NDC 72570 122 35, UPC 3 72570 12235 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V212000·2023-03-29

    Audi Recalls 2020 Q7 Vehicles Due to Front Camera Fire Risk

    Audi is recalling 2020 Q7 vehicles because a software incompatibility may cause the front camera heating element to overheat, increasing the risk of a fire.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0631-2023·2023-03-29

    Rice Crackers Recalled Due to Undeclared Wheat Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling IWATSUKASEIKA Ajishirabe Rice Crackers because the label fails to declare wheat. Wheat is a major allergen that can cause severe allergic reactions in sensitive individuals.

    Product
    IWATSUKASEIKA Ajishirabe Rice Crackers UPC: 4901037117746 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0628-2023·2023-03-29

    MEITO Lemon Tea Recalled Due to Undeclared Milk Allergen

    MEITO Lemon Tea 4-pack is being recalled because milk allergen was not declared on the label. Consumers with milk allergies should not consume this product.

    Product
    MEITO Lemon Tea 4 Pack UPC: 4902757413507 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0638-2023·2023-03-29

    ITOSEIKA Chocolate Chip Cookies Recalled for Undeclared Milk Allergen

    ITOSEIKA chocolate chip cookies are being recalled due to undeclared milk allergen on the label. Consumers with milk allergies should not consume this product.

    Product
    ITOSEIKA Chocolate chip cookies 10pieces UPC: 4901050111400 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V215000·2023-03-29

    2018-2021 Volkswagen Atlas Front Passenger Air Bag Sensor Fault

    Volkswagen is recalling certain 2018–2021 Atlas and 2020 Atlas Cross Sport vehicles because a wiring fault in the passenger occupant detection system may deactivate the front passenger air bag when the seat is occupied.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V218000·2023-03-29

    Kia Recalls 2015-2019 Soul EV Vehicles for Battery Fire Risk

    Kia is recalling 2015-2019 Soul EV vehicles with E400 batteries because an electrical short-circuit could cause a fire. Owners should contact Kia for a free software update or battery replacement.

    Product
    KIA — KIA SOUL EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0643-2023·2023-03-29

    Pistachio wasabi snack recalled for undeclared soy allergen

    SENNARIDO Green Snack Pistachio-Wasabi Flavor (90g) is recalled because soy is not declared on the label. Approximately 10,986 units were distributed across California, Washington, Nevada, Texas, New York, New Jersey, and Canada.

    Product
    SENNARIDO Green Snack Pistachio -Wasabi Flavor 90g UPC: 4974120431715 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0630-2023·2023-03-29

    Sesame sauce recalled due to undeclared wheat allergen

    Shinsei Additive Free Sesame Sauce is being recalled because wheat allergen was not declared on the product label. Consumers with wheat allergies who consume this product may experience allergic reaction.

    Product
    Shinsei Additive Free Sesame Sauce 22g UPC: 4901665004616 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0640-2023·2023-03-29

    SENNARIDO pistachio snack recalled for undeclared soy allergen

    DAISO CALIFORNIA WAREHOUSE is recalling SENNARIDO Green Snack Pistachio 90g because the product contains undeclared soy, a major food allergen that poses allergic reaction risk to sensitive consumers.

    Product
    SENNARIDO Green Snack Pistachio 90g UPC: 4974120413421 Made in Japan
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·23V213000·2023-03-29

    Volkswagen Recalls 2023 ID 4 Vehicles for Door Handle Water Ingress

    Volkswagen is recalling 2023 ID 4 vehicles because water can enter the door handle circuit board, causing doors to open unexpectedly at low speeds.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID 4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0637-2023·2023-03-29

    Meito Milk Cocoa Recalled for Undeclared Coconut Allergen

    Daiso California Warehouse is recalling Meito Milk Cocoa (12gX5P, UPC 4902757444709) because coconut allergen is not declared on the label. Consumers with coconut allergies should discontinue use and return the product.

    Product
    Meito Milk Cocoa 12gX5P (1stick bonus pack) UPC: 4902757444709 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1277-2023·2023-03-29

    Cardiosave Hybrid Intra-Aortic Balloon Pump Performance Issue Recall

    Datascope Corp. is recalling specific Cardiosave Hybrid intra-aortic balloon pumps due to a Safety Disk performance issue that may reduce balloon inflation and therapeutic benefit.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers Model Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0644-2023·2023-03-29

    Onishi Foods Alpha Rice Recalled for Undeclared Coconut Allergen

    Onishi Foods Alpha Rice Matsutake Mushroom Rice is being recalled because the label does not declare coconut, a major allergen. The recall affects 733 units distributed in multiple US states and Canada.

    Product
    Onishi Foods Alpha Rice Matsutake Mushroom Rice 100g UPC: 4970088140331 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1267-2023·2023-03-29

    DePuy Attune Tibial Insert Recalled for Excessive Radiation Exposure

    DePuy Orthopaedics is recalling Attune Posterior tibial insert implants that received excessive gamma radiation during manufacturing, which may degrade the material properties of the knee replacement component.

    Product
    Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM, Part Number 151640507
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0639-2023·2023-03-29

    Japanese Potato Yokan Candy Recalled for Undeclared Coconut

    Kinjo Seika Potato Yokan confection is being recalled because coconut, a major allergen, was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    Kinjo Seika Potato Yokan 130g UPC: 4901324017056 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1280-2023·2023-03-29

    Wearable ECG smartwatch software bug eliminates physician review

    Withings Scan Monitor/ScanWatch (model hwa09) has a software defect preventing physicians from reviewing ECG recordings, which is critical to the device's FDA clearance requirement for physician-supervised use. Users should discontinue use until the defect is corrected.

    Product
    Scan Monitor/ScanWatch, model number hwa09 Wearable, Bluetooth-connected wrist watch that records heart activity (ECG) and oxygen saturation (SpO2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0627-2023·2023-03-29

    Alpha Rice Mushroom Rice Recalled for Undeclared Coconut Allergen

    Onishi Foods Alpha Rice Mushroom Rice is recalled due to undeclared coconut allergen on the label. Consumers with coconut allergies should not consume this product.

    Product
    Onishi Foods Alpha Rice Mushroom Rice 100g UPC: 4970088140546 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0699-2023·2023-03-29

    Sprouts Farmers Market Saltine Crackers recalled for potential peanut contamination

    Sprouts Farmers Market is recalling Saltine Crackers Sea Salt Tops due to potential peanut contamination. Approximately 1,050 cases were distributed in Arizona, California, and Georgia.

    Product
    Sprouts Farmers Market Saltine Crackers Sea Salt Tops NET WT 16 OZ (1 LB) 454g UPC 646670310164 packaged in slug wrapper in a cardboard carton, 12 packages per case
    Category
    Food
    Distribution
    3 states
  • HighFDA (Drugs)·D-0472-2023·2023-03-29

    Daytrana methylphenidate patches recalled for defective delivery system

    Noven Pharmaceuticals is recalling Daytrana methylphenidate transdermal patches for a defective delivery system that fails to meet shear specifications. The recall affects specific lots distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0649-2023·2023-03-29

    WHH A&D Calcium Milk Drink Recalled for Undeclared Milk Allergen

    WHH A&D Calcium Milk Drink recalled due to undeclared milk on the ingredient label. The recall affects 12,000 units distributed in California.

    Product
    WHH A&D Calcium Milk Drink 220ml Plastic bottles 6 bottles in 1 pack Made in China
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1279-2023·2023-03-29

    Cardiosave IABP Pneumatic Interface Module Recalled for Performance Issue

    Datascope Corp. recalls the Cardiosave IABP Pneumatic Interface Module due to a Safety Disk performance issue that may reduce balloon inflation. Ten specific units with identified serial numbers are affected.

    Product
    Cardiosave Intra-Aortic Balloon Pump (IABP) Pneumatic Interface Module (PIM) , Model Number 0997-00-1178
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0642-2023·2023-03-29

    Kurata Menzo Ramen Recalled for Undeclared Coconut Allergen

    DAISO CALIFORNIA WAREHOUSE is recalling Kurata Menzo Meatfree Tonkotsu Ramen Dry due to undeclared coconut on the label. Consumers with coconut allergies who consume this product may experience allergic reactions.

    Product
    Kurata Menzo Meatfree Tonkotsu Ramen Dry 2P 238.8g UPC: 4906436004932 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0650-2023·2023-03-29

    DG Health Sugar Free Daily Fiber Recalled for Missing Phenylalanine Warning

    DG Health Sugar Free Daily Fiber is recalled for missing a required phenylalanine warning label. People with phenylketonuria (PKU) require this warning to safely use the product.

    Product
    DG Health brand Sugar Free Daily Fiber in 10 oz. plastic containers (UPC: 860005934294).
    Category
    Food
    Distribution
    47 states
  • HighFDA (Devices)·Z-1278-2023·2023-03-29

    Cardiosave IABP Safety Disk Model 0202-00-0140 Recalled for Performance Defect

    Datascope Corp. is recalling 669 Cardiosave IABP Safety Disks due to a performance defect that may reduce balloon inflation during cardiac support therapy. The affected devices may not provide adequate augmentation to patients requiring mechanical circulatory support.

    Product
    Cardiosave Intra-Aortic Balloon Pump (IABP) Safety Disk, Model Number 0202-00-0140
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1263-2023·2023-03-29

    Orthopedic Implant Recall: Excessive Radiation Exposure in Revision Tibial Insert

    DePuy Orthopaedics recalls 7 units of Attune Revision LPS Tibial Inserts (Part 151760118, Lot JP6452) distributed worldwide due to excessive gamma radiation during manufacturing. This overage may result in material property changes.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM, Part Number 151760118
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0645-2023·2023-03-29

    Russell Stover Sugar Free Peanut Butter Cups Recalled for Undeclared Tree Nuts

    Russell Stover Sugar Free Peanut Butter Cups are being recalled for undeclared tree nuts (pecans) on the outer packaging. The mislabeling poses a risk to consumers with tree nut allergies.

    Product
    Russel Stover Sugar Free Peanut Butter Cups packaged in 2.4oz peg bag, containing individually wrapped pieces. UPC 077260096937
    Category
    Food
    Distribution
    17 states
  • HighFDA (Drugs)·D-0473-2023·2023-03-29

    Daytrana Methylphenidate Transdermal Patches Recalled for Defective Delivery System

    Noven Pharmaceuticals recalls Daytrana (methylphenidate) 30 mg transdermal patches nationwide due to defective delivery system components that fail shear specifications. Patients should contact their healthcare provider regarding medication alternatives.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1284-2023·2023-03-29

    G7 Acetabular Liner Recalled for Size and Label Discrepancy

    Biomet recalled 12 units of its G7 Acetabular System 40mm Size D Liner because the actual implant is a 38mm Size C. The mismatch between outer labeling and the actual implant could result in wrong-size component placement during surgery.

    Product
    G7 Acetabular System, Dual Mobility Acetabular Liner, 40 mm, Size D, Model Number 110024462
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-1265-2023·2023-03-29

    Attune Revision Limb Preservation System Tibial Insert Recalled for Over-Irradiation

    DePuy Orthopaedics is recalling 7 units of the Attune Revision Limb Preservation System Tibial Insert (Lot JP9022) that received higher than specified gamma radiation doses. The over-irradiation may cause changes to implant material properties.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM, Part Number 151760226
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0626-2023·2023-03-29

    MEITO Alphabet Chocolate recalled for undeclared coconut allergen

    MEITO Alphabet Chocolate 50g packages sold in multiple U.S. states and Canada were distributed with undeclared coconut allergen. Consumers with coconut allergies should not consume this product.

    Product
    MEITO Alphabet Chocolate 50g 50g UPC: 4902757130909 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1276-2023·2023-03-29

    Cardiosave Hybrid intra-aortic balloon pump safety disk defect may reduce therapy efficacy

    Datascope's Cardiosave Hybrid intra-aortic balloon pump may have a faulty Safety Disk that reduces balloon inflation and cardiac augmentation. No injuries reported.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), Model Numbers 0998-00-0800-31, 0998-00-0800-32, 0998-00-0800-33, 0998-00-0800-35, 0998-00-0800-45, 0998-00-0800-52, 0998-00-0800-53, 0998-00-0800-55, and 0998-00-0800-65
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0647-2023·2023-03-29

    Butter Toffee Recalled for Undeclared Milk and Soy Allergens

    Bruttles Gourmet Candies Butter Toffee products lack allergen warnings for milk and soy. Consumers with allergies should not consume these products.

    Product
    Butter Toffee, net wt. 16 oz, 6 units per case. Label declares: Butter Toffee, Butter, Sugar, Corn Syrup, Almonds, Vanilla, Salt. www.bruttles.com. Butter Toffee, net wt. 4oz., part of Medium Samplers package. Product is packaged in cello bag and labeled Butter Toffee. Label de
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1272-2023·2023-03-29

    Disposable Patient Circuit with Precision Flow System recalled for excessive condensation

    Vapotherm has recalled 5,869 Low Flow Disposable Patient Circuits for the Precision Flow System due to reports of excessive condensation that may lead to rainout.

    Product
    Low Flow Disposable Patient Circuit for the Precision Flow System, Product Code PF-DPC-LOW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0634-2023·2023-03-29

    Coffee Candy Recalled for Undeclared Coconut Allergen

    Kanro Non sugar coffee candy is recalled because coconut was not declared on the label, posing a risk to consumers with coconut allergies.

    Product
    Kanro Non sugar coffee candy 40g UPC: 4901351013137 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1207-2023·2023-03-29

    BD Pyxis Automated Medication Dispensing Systems Firmware Downgrade Recall

    CareFusion recalls 7,914 units of BD Pyxis automated medication dispensing systems after firmware was inadvertently downgraded during installation, potentially causing drawer failures and medication delivery delays.

    Product
    BD Pyxis Anesthesia ES System (PAS ES), REF: 327; BP Pyxis MedStation ES (Med ES Main), REF: 323; BD Pyxis MedStation ES Tower (Med ES Tower), REF: 352; all with BD Pyxis ES version 1.6.1 drawer firmware (version 1.10.2.5). Pyxis MedStation Enterprise Server (ES) System is an a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0646-2023·2023-03-29

    BODYARMOR SportWater recalled for potential plastic pieces

    BA Sports Nutrition is recalling BODYARMOR SportWater due to potential plastic pieces in the product. The recall affects approximately 21 million bottles distributed across 11 states.

    Product
    BODYARMOR SportWater 24/700mL; BODYARMOR SportWater 12/1Liter; BODYARMOR SportWater 24/20oz 6PK; BODYARMOR SportWater 2x6/1 Liter; BODYARMOR SportWater 15/700mL Club; BODYARMOR SportWater 15/1L Club
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1266-2023·2023-03-29

    Attune Revision Tibial Insert Recalled for Excessive Gamma Radiation Exposure

    DePuy Orthopaedics is recalling 7 units of the Attune Revision Tibial Insert that received excess gamma radiation during manufacturing, which may degrade implant material properties.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM, Part Number 151760312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1264-2023·2023-03-29

    Orthopedic Tibial Insert Recalled Due to Excessive Radiation Exposure

    DePuy Orthopaedics is recalling Attune Revision LPS Tibial Insert devices (Lot JP9016) because they received excessive gamma radiation during manufacturing, which may compromise material properties.

    Product
    Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM, Part Number 151760212
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1281-2023·2023-03-29

    Raystation Treatment Planning System Collimator Angle Export Defect

    Raystation radiation therapy planning software may not correctly export collimator angle settings when using the DICOM export function. In exported files, the collimator angle may be replaced with zero regardless of the user's selection.

    Product
    Raystation treatment planning system for radiation therapy, Model Numbers 9.0.0, 9.0.1, 9.1.0, 9.2.0, 10.0.0, 10.0.1, 10.0.2, 10.1.0, 10.1.1, 11.0.0, 11.0.1, 11.0.3, 11.0.4, 12.0.0, 12.1.0, 12.1.1, 12.0.3, 12.1.2, 12.0.4, 12.1.3, 13.0.0, 13.1.0. Software Version Numbers 9A, 9B,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V214000·2023-03-29

    2022 Volkswagen Taos Fuel Pump May Cause Engine Stall

    Volkswagen is recalling certain 2022 Taos vehicles because the fuel delivery pump may break and cause a sudden engine stall, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0468-2023·2023-03-29

    Prescription Drug Recall: Jardiance Empagliflozin 25 mg Label Mix-Up

    Boehringer Ingelheim Pharmaceuticals is recalling Jardiance (Empagliflozin) 25 mg tablets due to a label mix-up affecting 69,375 bottles distributed nationwide.

    Product
    JARDIANCE — JARDIANCE (EMPAGLIFLOZIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V211000·2023-03-29

    BMW seats may not restrain occupants properly in crash

    BMW is recalling certain 2019–2021 3-series and X3/X4 models because the seat frame may not have been welded properly to the seat rails, risking occupant injury in a crash.

    Product
    BMW — BMW X4, 330I, X3, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0641-2023·2023-03-29

    Igarashiseimen Kitakata Spicy Umakara Ramen Recalled for Undeclared Coconut Allergen

    Igarashiseimen Kitakata Spicy Umakara Ramen is being recalled because coconut allergen is not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    Igarashiseimen Kitakata Spicy Umakara Ramen UPC: 4967448174211 Made in Japan
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0648-2023·2023-03-29

    Kirkland Signature Colombian cold brew coffee recalled for metal contamination

    Berner Foods Inc. is recalling Kirkland Signature Colombian Cold Brew Coffee due to metal contamination in 231,071 cases distributed across 13 states. Consumers should stop using affected products.

    Product
    Kirkland Signature Colombian Cold Brew Coffee ready-to-drink, 12 fl oz in aluminum can, 12 cans per case
    Category
    Food
    Distribution
    13 states
  • HighFDA (Drugs)·D-0471-2023·2023-03-29

    Daytrana Methylphenidate Patches Recalled for Defective Transdermal Delivery System

    Noven Pharmaceuticals is recalling specific lots of Daytrana (methylphenidate) transdermal patches due to a defective delivery system that is out of specification for shear. Affected lots are Lot 91956 (6/2023) and Lot 92475 (7/2023), distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0636-2023·2023-03-29

    Soft rice crackers recalled for undeclared coconut allergen

    DAISO CALIFORNIA WAREHOUSE is recalling 150YEN HIZATSUKI Soft rice crackers because the product contains coconut that was not declared on the label. Consumers with coconut allergies should not consume this product.

    Product
    150YEN HIZATSUKI Soft rice crackers sea lettuce soy sauce flavor UPC: 4902445210500 Made in Japan
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1283-2023·2023-03-29

    DeRoyal Suction Canister Recalled Due to Lid Shrinkage Seal Defect

    DeRoyal SafeLiner Suction Canister model PHESL-1000B is being recalled due to lid shrinkage that prevents proper vacuum seal formation and maintenance. The recall affects 27,200 devices distributed across multiple US states.

    Product
    DeRoyal SafeLiner Suction Canister, 1000cc, REF PHESL-1000B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0470-2023·2023-03-29

    Daytrana Methylphenidate Patches Recalled for Defective Delivery System

    Noven Pharmaceuticals is recalling specific lots of Daytrana methylphenidate transdermal patches distributed nationwide because the delivery system is out of specification for shear. The affected lots require patient and healthcare provider attention.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0624-2023·2023-03-29

    Haiyue Preserved Vegetable Product Recalled for Unauthorized Food Additive

    Haiyue Food Nutritional Preserved Vegetable is recalled because it contains cyclamate, an unauthorized food additive in the United States. The FDA Class III recall affects 55 boxes distributed in New York, North Carolina, Florida, and Indiana.

    Product
    Haiyue Food Nutritional Preserved Vegetable
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-1282-2023·2023-03-29

    Contact Lens Recall: CooperVision Clariti 1-day Toric With Incorrect Power

    CooperVision is recalling Clariti 1-day toric contact lenses from lot W0124677 because they were made with a misaligned axis that results in incorrect lens power.

    Product
    Clariti 1-day toric soft contact lenses, Power -1.00 -1.25/90
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0474-2023·2023-03-29

    Dofetilide Capsules Recalled for Failed Content Uniformity Specifications

    Sun Pharmaceutical is recalling 1,920 bottles of Dofetilide Capsules (500 mcg) nationwide due to failed content uniformity specifications, meaning the capsules do not contain uniform amounts of active ingredient.

    Product
    Dofetilide Capsules, 500 mcg (0.5 mg), 60-count bottle, Rx only, Manufactured by: Sun Pharmaceutical Industries Limited, Survey No. 259/15, Dadra-396 191, (U.T. of D & NH), India, NDC 47335-0063-86
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V208000·2023-03-28

    Freightliner Cascadia and Western Star 49X hazard light malfunction recall

    Daimler Trucks North America is recalling 2020-2021 Freightliner Cascadia and Western Star 49X vehicles because hazard warning lights may flash improperly during Advanced Braking Assist events, potentially confusing other drivers and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 49X, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V210000·2023-03-28

    2023 Genesis G90 seat belt pretensioners may explode during crashes

    Hyundai is recalling 575 units of the 2023 Genesis G90 because the seat belt pretensioners may explode in a crash. Metal fragments from the explosion may strike and injure vehicle occupants.

    Product
    GENESIS — GENESIS G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·011-2023·2023-03-24

    Elkhorn Valley Packing Recalls Boneless Beef Chuck Due to E. coli O103

    Elkhorn Valley Packing is recalling approximately 3,436 pounds of boneless beef chuck product due to possible contamination with Shiga toxin-producing E. coli (STEC) O103.

    Product
    Elkhorn Valley Packing LLC — Elkhorn Valley Packing Recalls Boneless Beef Chuck Product Due to Possible E. coli O103 Contamination
    Category
    Food
    Distribution
    9 states
  • SevereNHTSA·23V198000·2023-03-24

    2023 Ford Edge child restraint system tether welds insufficient

    Ford is recalling certain 2023 Edge vehicles because child seat tether welds may be insufficient, potentially reducing proper child restraint during a crash. Dealers will replace the seat back frame free of charge.

    Product
    FORD — FORD, LINCOLN EDGE, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V201000·2023-03-24

    Forest River Recalls 2023 Pause Travel Trailers Due to Wiring Defect

    Forest River is recalling 2023 Pause travel trailers because a wiring error may prevent the breakaway switch from activating trailer brakes, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER PAUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V200000·2023-03-24

    Mercedes-Benz Recalls 2021 S 580 Vehicles for Water Intrusion Defect

    Mercedes-Benz is recalling 2021 S 580 and Maybach S 580 vehicles because water may enter the passenger compartment, potentially disabling safety features.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 580
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V202000·2023-03-24

    Forest River Recalls 2023 Pause Travel Trailers Due to Brake Wire Defect

    Forest River is recalling 2023 Pause travel trailers because an incorrectly routed brake wire may pinch, potentially causing brake failure and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER PAUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V197000·2023-03-24

    Shadow Living Quarter Trailers Recalled for Gas Leak Risk

    Shadow Trailer is recalling 2016-2023 Living Quarter trailers because cooktop burner tubes may fracture and leak gas, increasing fire risk.

    Product
    SHADOW — SHADOW LIVING QUARTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V203000·2023-03-24

    Jayco Northpoint Fifth Wheel Recall for Axle U-Bolt Tightening Issues

    Jayco is recalling 2023 Northpoint FW travel trailers because improperly tightened axle U-bolts may allow the axle to move, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL NORTH POINT
    Category
    Vehicle
    Distribution
    Distributed nationwide

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