The Recall Desk

Archive

December 2023 recalls

600 recalls were announced in December 2023.

What the numbers show

Critical
29
Severe
210
High
310
Moderate
49
Low
2

Of the 600 recalls this month scored against our rubric, 5% are Critical, 35% are Severe.

Which agencies issued them

101–200 of 600

  • HighFDA (Devices)·Z-0566-2024·2023-12-27

    CardioQuip Modular Cooler-Heater Model MCH-1000(m) Recalled for Bacterial Contamination

    CardioQuip LLC is recalling 2 units of its Model MCH-1000(m) Modular Cooler-Heater due to potential bacterial contamination that could result in patient infection. The affected devices are distributed in California, Texas, Pennsylvania, Washington, Ohio, and Nebraska.

    Product
    CardioQuip Modular Cooler-Heater, Model: MCH-1000(m), Power: 115V-60Hz, 16A
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0565-2024·2023-12-27

    CardioQuip Modular Cooler-Heater Device Recalled for Potential Bacterial Contamination

    CardioQuip is recalling the Modular Cooler-Heater (Model MCH-1000i) due to potential bacterial contamination that could cause patient infection. Four units were distributed in California, Texas, Pennsylvania, Washington, Ohio, and Nebraska.

    Product
    CardioQuip Modular Cooler-Heater, Model: MCH-1000(i), Power: 115V-60Hz, 16A
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Food)·F-0607-2024·2023-12-27

    Frozen vegetarian pizza recalled for undeclared wheat allergen

    Shakespeare's Pizza Vegetarian Pizza is being recalled because it contains undeclared wheat, a common allergen. Affected products were distributed to retail stores in Missouri and Kansas and through online direct sales.

    Product
    Shakespeare's Pizza, Vegetarian Pizza, 25 oz, Keep Frozen; UPC 686 148 007 394; pack size 18 per case.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0567-2024·2023-12-27

    AC Power Adapter for LIFEPAK 15 Defibrillator May Fail to Charge or Power On

    AC power adapters for LIFEPAK 15 Monitor/Defibrillators may fail to charge batteries or power on the device. Physio-Control is recalling 18,732 units manufactured between November 2021 and April 2023.

    Product
    AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0155-2024·2023-12-27

    Nystatin Powder Recall Due to Incorrect Assay Strength on Label

    Fagron, Inc. is recalling 46 containers of Nystatin 500 MU bulk powder used for prescription compounding due to an incorrect assay value on the product label. The mislabeled strength could affect proper compounding of patient medications.

    Product
    NYSTATIN 500 MU, Activity (as is): 6482 Units/mg, bulk powder container, Rx Only, For Prescription Compounding, Fagron, Inc. - 2400 Pilot Knob Rd. St Paul, MN 55120. NDC 51552-0041-3, Bar code 3 51552 00413 9
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0577-2024·2023-12-27

    AcuMatch Hip System Recalled for Loss of Vacuum Integrity

    Exactech is recalling AcuMatch Hip System devices due to loss of vacuum in the inner-most vacuum bag, with 3 complaints reported affecting 4 devices. Vacuum loss could compromise device packaging integrity.

    Product
    AcuMatch Hip System, Catalog Number 142-32-27
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0576-2024·2023-12-27

    Philips Inclusive CT Systems: Software Errors in Image Display and Interpretation

    Philips North America is recalling 330 Philips Inclusive CT imaging systems due to software issues causing incorrect image display, errors in image interpretation, and patient exposure to incorrect images and system functions during clinical use.

    Product
    The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into cross-sectional images of the body taken at different angles and planes. The system also includes signal analysis and display equipment, patient and equipment suppor
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Devices)·Z-0580-2024·2023-12-27

    Exactech Equinoxe Shoulder System recalled for loss of vacuum

    Exactech is recalling specific models of its Equinoxe Shoulder System implants due to loss of vacuum in the inner-most vacuum bag. Four devices have been affected according to three complaints received.

    Product
    Exactech Equinoxe Shoulder System, Catalog Numbers: a) 314-23-02, b) 314-23-03, c) 314-23-13, d) 314-23-14, e) 314-23-15, f) 314-24-22, g) 314-24-23, h) 314-24-24, i) 314-24-32, j) 314-24-33, k) 314-24-34, l) 314-24-35
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0559-2024·2023-12-27

    Philips Azurion Ceiling-Mount Systems Rotation Cover May Fall

    Philips is recalling Azurion ceiling-mount imaging systems because a rotation cover may fall if the L-arm collides with hospital equipment, potentially causing injury or affecting sterilization.

    Product
    Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion 7 M12 722079 Azurion 7 M20 722223 Azurion 7 M12 722224 Azurion 7 M20 722227 Azurion 5 M12 722228 Azurion 5 M20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0608-2024·2023-12-27

    RAPIDPoint 500 Measurement Cartridge Sodium Sensor May Cause Measurement Error

    Siemens RAPIDPoint 500 cartridges may produce inaccurate sodium measurements in blood samples, potentially delaying diagnosis or causing inappropriate treatment. The sodium sensor may show a negative bias, affecting patient care.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491448
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0639-2024·2023-12-27

    Vegan pumpkin pie products recalled due to foreign object contamination

    Willamette Valley Pie Company is recalling vegan pumpkin pie products distributed in 12 states due to foreign object contamination. The voluntary recall was initiated in November 2023.

    Product
    Bulk Frozen Cases: The 9" Vegan Pumpkin Pie bulk case has UPC 22518 84081 and the label is read in parts: 9" Vegan Pumpkin Pie WFM, BAKED BULK, 6 units/case. KEEP FROZEN - TRANSPORT AND STORE AT LESS THAN ZERO DEGREES F. Just Thaw and serve. Remove from freezer, removed plastic w
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-0640-2024·2023-12-27

    Candy Shop Rainbow Belts recalled for undeclared gluten in gluten-free product

    Island Snacks, Inc. is recalling The Candy Shop Rainbow Belts because the product is labeled gluten-free but contains modified wheat flour. This poses a risk to consumers with celiac disease or gluten sensitivity.

    Product
    The Candy Shop Rainbow Belts Net Wt. 10.5 oz. (298g) SKU Code: 400255786276
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0585-2024·2023-12-27

    Exactech Truliant Knee System Recalled Due to Vacuum Bag Failure

    Exactech recalls certain Truliant Knee System units due to loss of vacuum in the inner vacuum bag. The affected units were distributed across multiple U.S. states and international locations.

    Product
    Exactech Truliant Knee System, Catalog Numbers: a) 02-012-35-3509, b) 02-022-35-1509, c) 02-022-35-1513, d) 02-022-35-3010, e) 02-022-35-3509, f) 02-022-35-3510, g) 02-022-35-3511, h) 02-022-35-4511, i) 02-022-44-3512, j) 02-022-47-2509, k) 02-022-51-4519
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0587-2024·2023-12-27

    Exactech Vantage Ankle System Recalled Due to Vacuum Loss

    Exactech is recalling two catalog numbers of Vantage Ankle System devices due to loss of vacuum in the inner-most vacuum bag. Three complaints have been received relating to four affected devices.

    Product
    Exactech Vantage Ankle System, Catalog Numbers: a) 350-21-04, b) 350-22-03
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0604-2024·2023-12-27

    Abbott Hematology Analyzers Recalled for Unlabeled Latex Component

    Abbott CELL-DYN Ruby and Sapphire hematology analyzers contain latex that is not labeled on the device, posing a risk to users with latex allergies. The recall affects 670 devices distributed across 33 states, Puerto Rico, and Brazil.

    Product
    Abbott CELL-DYN Ruby, Model CD-Ruby, List number 08H67-01, and Abbott CELL-DYN Sapphire, Model CD Sapphire, list number 08H00-01. Multi-parameter, automated hematology analyzer.
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0582-2024·2023-12-27

    Exactech Optetrak Knee Implant System Recalled for Vacuum Seal Failure

    Exactech is recalling specific catalog numbers of the Optetrak Knee Implant System due to loss of vacuum in the protective inner bag. Three complaints affecting four devices have been reported.

    Product
    Exactech Optetrak Knee System, Catalog Numbers: a) 200-02-26, b) 200-02-29, c) 200-02-32, d) 200-02-35, e) 200-02-38, f) 200-02-41, g) 200-03-32, h) 200-07-29, i) 200-07-32, j) 200-07-35, k) 204-21-13, l) 204-22-26, m) 208-23-18, n) 208-24-13
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Food)·F-0606-2024·2023-12-27

    Frozen Spinach Artichoke Pizzas Recalled for Undeclared Wheat

    Shakespeare's Pizza recalls 7,103 units of frozen Spinach Artichoke Pizza sold in Missouri and Kansas due to undeclared wheat. Consumers with wheat allergies should not consume the product.

    Product
    Shakespeare's Pizza, Spinach Artichoke Pizza, 25 oz, Keep Frozen; UPC 686 148 000 043; pack size 18 per case.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0610-2024·2023-12-27

    LITe Decompression Snake Arm cannot attach due to incorrect clamp component

    Stryker Spine is recalling 9 units of the LITe Decompression Snake Arm due to an incorrect clamp component that prevents proper attachment to the arm post shaft. Affected units were distributed in the US and internationally.

    Product
    LITe Decompression Snake Arm, REF 48080230
    Category
    Medical Device
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0595-2024·2023-12-27

    CARDIOHELP-i Heart-Lung Support System not properly tested for leakage current

    The CARDIOHELP-i Heart-Lung Support System was not properly tested to measure leakage current, an electrical safety concern. The FDA is recalling 1,594 units distributed worldwide.

    Product
    CARDIOHELP-i Heart Lung Support System: Blood oxygenation and carbon dioxide removal system used to pump blood through the extracorporeal bypass circuit for circulatory and/or pulmonary support for periods appropriate to cardiopulmonary bypass (up to six hours). Product REF Numb
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0603-2024·2023-12-27

    ZEUS ELISA Parvovirus B19 Test Kits Recalled for Unapproved Modification

    Zeus Scientific recalls ZEUS ELISA Parvovirus B19 IgM test kits due to an unapproved modification to the test conjugate that was implemented without FDA review and approval.

    Product
    ZEUS ELISA Parvovirus B19 IgM Test System, Product Number SM9Z7701G
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0564-2024·2023-12-27

    Vero Biotech GENOSYL DS cassette recalled for manufacturing flow defect

    Vero Biotech is recalling GENOSYL DS Generation 3 cassettes that failed to meet manufacturing flow specifications. The recall affects 2 units distributed in Arizona and Florida.

    Product
    VERO BIOTECH GENOSYL DS (Delivery System) Generation 3 Cassette, Model Number 602722-01; generates and delivers nitric oxide (NO) for inhalation at the point of use
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-0602-2024·2023-12-27

    ZEUS ELISA Parvovirus B19 Test Kits Recalled for Unapproved Modification

    Zeus Scientific is recalling 296 ZEUS ELISA Parvovirus B19 IgG Test System kits distributed in seven US states because an unapproved modification was made to the test reagent without FDA approval.

    Product
    ZEUS ELISA Parvovirus B19 IgG Test System, Product Number SM9Z7701M
    Category
    Medical Device
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0560-2024·2023-12-27

    Roche Cobas Interface Module Firmware May Cause Delayed Sample Processing

    Inpeco is recalling firmware versions for the Roche Cobas 8000 and PRO Interface Module that may cause delayed sample tube processing in laboratory automation systems.

    Product
    Roche Cobas 8000 and Cobas PRO Interface Module (CO8 IM)- IVD FlexLab Automation System -a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. Hardware versions: FLX-247-0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0568-2024·2023-12-27

    ACMI Roller Bar Electrodes Recall Due to Incorrect Pouch Labeling

    Olympus Corporation of the Americas is recalling ACMI Roller Bar Electrodes due to incorrect pouch labels. Pouches are mislabeled as Right Angle Cutting Loop Electrodes but contain the correct Roller Bar product.

    Product
    ACMI Roller Bar Electrodes bearing incorrect pouch label of ACMI USA Elite System and USA Series Right Angle Cutting Loop Electrode Stabilized, 0.012 Wire 24 Fr (8mm), Model: REF MLE 24-012. Product packaged in boxes of 6 pouches. Box of 6 has correct box label of ACMI USA Elite
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-0586-2024·2023-12-27

    Exactech knee replacement inserts recalled for vacuum seal loss

    Exactech is recalling Truliant and Activit-E knee replacement inserts for loss of vacuum in storage packaging. The defect was identified in 3 complaints involving 4 devices, with no reported injuries.

    Product
    Exactech Truliant, Activit-E Knee Insert, Catalog Numbers: a) 02-023-02-0029, b) 02-023-02-0032, c) 02-023-02-0035, d) 02-023-02-0038, e) 02-024-35-1512, f) 02-024-35-1515, g) 02-024-35-1519, h) 02-024-35-2010, i) 02-024-35-2013, j) 02-024-35-2015, k) 02-02
    Category
    Medical Device
    Distribution
    16 states
  • ModerateFDA (Food)·F-0603-2024·2023-12-27

    Ice Cream Bar Recalled for Undeclared Food Dyes

    La Michoacana Rompope ice cream bars are being recalled due to undeclared Yellow #5, Yellow #6, and Red #40. The product was distributed only in Florida.

    Product
    ICE CREAM BAR, MICHOACANA, es...natural, ROMPOPE, Net. Wt. 6 Fl. Oz., Packaged in a plastic bag. Frozen.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V900000·2023-12-26

    Volvo Recalls One 2020 VNL Truck for Steering Gear Assembly Defect

    Volvo Trucks North America is recalling one 2020 VNL truck because the steering gear assembly may have been assembled with fewer recirculating balls than required, potentially causing a loss of steering control.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V899000·2023-12-26

    2024 Mack Commercial Trucks Steering Gear Assembly Defect Recall

    Mack is recalling approximately 284 certain 2024 Pinnacle, Anthem, and Terrapro commercial trucks with incorrectly assembled steering gear assemblies that could cause loss of steering control and increase crash risk. Dealers will inspect and replace defective gears free of charge.

    Product
    MACK — MACK ANTHEM (AN), PINNACLE (PI/PN), TERRAPRO (TE)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V901000·2023-12-26

    2024 Hyundai Kona: Battery Cable Chafing May Cause Engine Fire

    Hyundai is recalling 2024 Kona vehicles because battery cables may chafe and short circuit, increasing the risk of engine compartment fire. Dealers will install protective sheathing at no cost.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·064-2023·2023-12-22

    Scanga Meat Company Recalls Ground Beef Due to E. Coli O103

    Scanga Meat Company is recalling approximately 563 pounds of ground beef products sold in Colorado due to possible E. coli O103 contamination.

    Product
    Scanga Meat Company — Scanga Meat Company Recalls Ground Beef Products Due to Possible E. Coli O103 Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V898000·2023-12-22

    New Flyer Transit Buses Recalled for Unintended Acceleration Risk

    New Flyer is recalling 211 transit buses from 2022-2023 due to a software error that may cause unintended acceleration, increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XE35, XN40, XN35, XE40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V895000·2023-12-22

    Freightliner M2 Recall: Incorrect Gear Shifter May Cause Rollaway

    Daimler Trucks is recalling 2,547 2024 Freightliner M2 vehicles because an incorrect gear shifter may allow the vehicle to roll away when in Park.

    Product
    FREIGHTLINER — FREIGHTLINER M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V897000·2023-12-22

    New Flyer Recalls 2021-2023 XE Buses for Unintended Acceleration

    New Flyer is recalling 246 battery electric transit buses due to a software error that may cause unintended acceleration, increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XE40, XE35, XE60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V894000·2023-12-22

    Rosenbauer Fire Apparatus Recalled for Electrical Circuit Overload Risk

    Rosenbauer America is recalling specific fire apparatus models due to a firmware defect that can cause electrical circuits to overload and overheat, increasing the risk of fire.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, COMMERCIAL F-350, COMMERCIAL F-550, WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V887000·2023-12-22

    Mack Trucks Recalls 2024 Granite Vehicles for Steering Knuckle Defect

    Mack Trucks is recalling 2024 Granite vehicles because bearing journals may not be fully seated in the steering knuckle assembly, which can lead to axle spindle fracture and increased crash risk.

    Product
    MACK — MACK GRANITE (GR)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V905000·2023-12-22

    Ford vehicles recalled for oil pump belt failure and power braking loss

    Certain 2016-2018 Ford Focus and 2018-2022 Ford EcoSport vehicles may have faulty oil pump drive belts or tensioners that can fail, causing engine stall and loss of power braking assist, increasing crash risk.

    Product
    FORD — FORD ECOSPORT, FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V884000·2023-12-22

    BMW Recalls 2021-2024 R 18 Motorcycles for Headlight Defect

    BMW is recalling 2,369 motorcycles because headlight attachment points may break, causing insufficient illumination and increasing crash risk.

    Product
    BMW — BMW R 18 B, R 18 TRANSCONTINENTAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V885000·2023-12-22

    2024 BMW i5 Electric Vehicles Pedestrian Warning Sound System May Fail

    BMW is recalling 2024 i5 electric vehicles where the external pedestrian warning sound generator may fail during startup. This could leave pedestrians unaware of approaching vehicles, increasing injury risk.

    Product
    BMW — BMW I5 M60, I5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V892000·2023-12-22

    Alamo Recalls Old Dominion Brush Units Due to Hoist Bolt Failure Risk

    Alamo Group is recalling 2021-2023 Old Dominion Brush Company units because a hoist bolt can shear, causing the dump body to drop and potentially injure people.

    Product
    OLD DOMINION BRUSH CO. — OLD DOMINION BRUSH CO. TRUCK MOUNTED UNIT, TRAILER MOUNT UNIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V893000·2023-12-22

    Mercedes-Benz Tourrider Coaches Recalled for Unsecured 120-Volt Outlets

    Daimler Coaches is recalling 2022-2024 Mercedes-Benz Tourrider coaches because 120-volt outlets may detach, posing a shock hazard to passengers.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ TOURRIDER BUSINESS, TOURRIDER PREMIUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V830000·2023-12-22

    2023 Kia Soul Side Curtain Airbags May Deploy Unexpectedly

    Kia is recalling 2023 Soul and 2024 Seltos vehicles because side curtain airbags may deploy unexpectedly due to a manufacturing error, increasing the risk of injury or crash. Dealers will replace affected modules free of charge.

    Product
    KIA — KIA SOUL, SELTOS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V889000·2023-12-22

    Prevost Bus Wheelchair Lift Warning Beacon May Be Insufficiently Bright

    Prevost is recalling certain H3-41, H3-45, X3-45, and X3-45 Commuter vehicles from 2012–2024. The red warning beacon on the wheelchair lift may not be bright enough, potentially making the lift less visible to users.

    Product
    PREVOST — PREVOST X3-45, X3-45 COMMUTER, H3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24064·2023-12-21

    Brandline HEAO 4-in-1 High Chairs Recalled for Suffocation and Laceration Risks

    Brandline is recalling about 820 HEAO 4-in-1 high chairs sold on Amazon from November 2022 through September 2023 because they pose suffocation, finger laceration, and entrapment hazards. One child has suffered a laceration requiring medical attention.

    Product
    HEAO 4-in-1 High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24065·2023-12-21

    Hover-1 Helix Hoverboards Recalled Due to Fire Hazard

    About 25,000 Hover-1 Helix hoverboards in Camouflage and Galaxy colors are recalled because their lithium-ion batteries can overheat and catch fire. Three fires have been reported, along with smoke inhalation injuries and property damage.

    Product
    Hover-1 Helix hoverboards (Camouflage and Galaxy colors only)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V877000·2023-12-21

    Kia Recalls 2011 Sorento Vehicles Due to Engine Fire Risk

    Kia is recalling 2011 Sorento vehicles because an engine compartment fire can occur while driving, increasing the risk of injury.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V873000·2023-12-21

    REV Ambulance Recalls 2020-2024 Models Due to Electrical Fire Risk

    REV Ambulance Group Orlando is recalling 210 Type I, III, and IX ambulances from 2020-2024 because a firmware defect can cause electrical fires.

    Product
    REV AMBULANCE — REV AMBULANCE TYPE IX, TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V878000·2023-12-21

    Mercedes-Benz Recalls 2023-2024 Models for Fuel Pump Seal Defect

    Mercedes-Benz is recalling 2023 GLC 300 and 2024 GLE 350/450 vehicles because incorrect screws may prevent a proper seal on the high-pressure fuel pump, risking leaks and fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450, GLE 350, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V883000·2023-12-21

    2022 Rivian R1S accelerator pedal may fail to detect driver release

    The accelerator pedal in 2022 Rivian R1S and R1T vehicles may fail to detect pedal release, preventing auto-hold and park functions from activating and increasing crash risk.

    Product
    RIVIAN — RIVIAN R1S, R1T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V870000·2023-12-21

    GM Recalls 2014 Buick Verano and Chevrolet Cruze for Air Bag Defect

    General Motors is recalling 2014 Buick Verano and Chevrolet Cruze vehicles because side roof-rail air bag inflators may rupture, posing an injury risk.

    Product
    CHEVROLET — CHEVROLET, BUICK CRUZE, VERANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V874000·2023-12-21

    2020 Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Propeller Shaft Defect

    Daimler Vans USA is recalling 2020 Mercedes-Benz and Freightliner Sprinter vans because a propeller shaft connection may loosen, reducing vehicle control and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 4500, SPRINTER 2500, SPRINTER 3500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V875000·2023-12-21

    Daimler Recalls 2019-2021 Sprinter Vans for Frame Fastener Defect

    Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans because missing frame fasteners may reduce stability and structural integrity.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500, SPRINTER 1500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V872000·2023-12-21

    2024 Land Rover Range Rover Sport body panel bonding defect affects passenger safety

    Jaguar Land Rover is recalling certain 2024 Land Rover Range Rover and Range Rover Sport vehicles because body panels may not be bonded properly, reducing structural strength and increasing crash injury risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24732·2023-12-21

    Pella Architect Series Casement Windows Recalled for Detachment Injury Hazard

    Pella Corporation is recalling approximately 12,000 Architect Series Casement Windows because the window sash can detach from the frame and fall, creating an injury risk. The company has received one report of detachment but no injuries have been reported.

    Product
    Pella Architect Series Casement Windows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V871000·2023-12-21

    2023 Land Rover Range Rover Sport Exterior Lights May Fail

    Moisture may accumulate in the right-side tailgate and lights of certain 2023 Land Rover Range Rover Sport vehicles, causing exterior lights to fail and reducing visibility.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24067·2023-12-21

    Klein Tools and Blackfire Portable Power Stations Recalled for Fire and Burn Hazards

    Klein Tools and Blackfire portable rechargeable power stations are being recalled because their internal inverter boards can overheat, creating fire and burn hazards. Consumers should stop using the units and return them to their original point of purchase.

    Product
    Portable Rechargeable Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V879000·2023-12-21

    Daimler Recalls 2023-2024 Electric Transit Buses Due to Inverter Cable Issue

    Daimler Trucks North America is recalling 26 electric transit buses because a high-voltage inverter cable may not be secured properly, potentially causing a loss of drive power.

    Product
    FCCC — FCCC, THOMAS BUILT BUSES MT50E, SAF-T-LINER C2 JOULEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24737·2023-12-21

    Litti City and Litti Pritti Dress-Up Playsets and Prextex Slime Eggs Recalled for Phthalate and Lead Violations

    Litti City Premier Doctor and Teacher Purse playsets, Litti Pritti Stylist Handbag set, and Prextex Slime Eggs are recalled for containing phthalates and lead exceeding federal safety standards. No injuries have been reported.

    Product
    Litti City Premier Doctor Playset and Teacher Purse Set, Litti Pritti Stylist Handbag Set, and Prextex Slime Eggs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24066·2023-12-21

    FeraDyne Outdoors Recalls Rhino Tree Stands Due to Fall Hazard

    FeraDyne Outdoors is recalling about 50,000 Rhino Tree Stands because the safety harness stitching can rip, creating a fall hazard. No injuries have been reported.

    Product
    Rhino Tree Stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V880000·2023-12-21

    Mercedes-Benz vehicles recalled for fuel pump failure affecting drive power

    Mercedes-Benz is recalling 2021–2024 vehicles due to fuel pump failures that may cause loss of drive power, increasing crash risk. Dealers will provide free replacement.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH GLE 350, GLE 580 4MATIC, GLS 450 4MATIC, GLS 580 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V869000·2023-12-21

    2024 Chevrolet Equinox door strikers may fracture and open unexpectedly

    General Motors is recalling certain 2024 Chevrolet Equinox and related models because door strikers may fracture, potentially causing doors to open unexpectedly while driving.

    Product
    CHEVROLET — CHEVROLET, GMC BLAZER, EQUINOX, TERRAIN, BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V881000·2023-12-21

    2022-2023 Mercedes-Benz Metris Fuel Pump May Fail Unexpectedly

    The fuel pumps in certain 2022-2023 Mercedes-Benz Metris vehicles may shut down unexpectedly, causing loss of drive power and increasing the risk of a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V876000·2023-12-21

    Mercedes-Benz and Freightliner Sprinter Partition Wall Recall for Missing Bolts

    Daimler Vans USA is recalling 2019-2023 Mercedes-Benz and 2019-2021 Freightliner Sprinter vehicles whose partition walls may have missing bolts. The loose wall could detach during a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, SPRINTER 1500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V882000·2023-12-21

    2024 Nissan Altima Recall for Potential Steering Bolt Loosening

    Nissan is recalling approximately 5 certain 2024 Altima vehicles because bolts connecting the electronic power steering unit to the steering rack may loosen, potentially causing loss of steering control or lock-up. Dealers will replace the steering gear assembly at no cost.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24068·2023-12-21

    TJX Foldable Wood and Rope Bistro Set Chairs Recall Due to Fall Hazard

    TJX is recalling about 29,000 foldable wood and rope bistro set chairs because the wooden frame can break or collapse when occupied, creating a fall hazard. The company has received eight reports of frame breakage, including six reports of minor injuries such as bruising and ankle strain.

    Product
    Foldable wood and rope bistro set chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0587-2024·2023-12-20

    Mixed Fruit Products Containing Cantaloupe Recalled for Salmonella

    Cut Fruit Express is recalling mixed fruit products containing cantaloupe that may be contaminated with Salmonella. The products were distributed in Illinois, Minnesota, and Wisconsin.

    Product
    Mixed Fruit Products that contain Cantaloupe, Honeydew, Pineapple, and Watermelon, Identified with the following Item ID and Description. 4702 Four Fruit CHPW
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·F-0524-2024·2023-12-20

    Wilcox Ice Cream Bar Recalled for Possible Listeria Contamination

    Wilcox Ice Cream Bar (Dairy Based) - Vanilla may be contaminated with Listeria monocytogenes. Consumers with best-by dates from September 15, 2024, through November 14, 2024, should not consume the product.

    Product
    Wilcox Ice Cream Bar (Dairy Based) - Vanilla; UPC 043726005041
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0592-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies found in gift baskets due to undeclared tree nuts. The cookies were distributed nationwide to all U.S. states.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #343 Brownie, Cookie & Cake Assortment
    Category
    Food
    Distribution
    50 states
  • CriticalFDA (Food)·F-0599-2024·2023-12-20

    Maggi 2-Minute Noodles Recalled for Undeclared Peanut Allergen

    Maggi 2-Minute Noodles sold in California are being recalled for undeclared peanut allergen. Consumers with peanut allergies should not consume this product.

    Product
    Maggi 2-Minute Noodles; 560g (12 packets per case); plastic pouch; store in a cool dry place
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0511-2024·2023-12-20

    Wilcox Premium Sea Salt Caramel Ice Cream Recalled for Listeria Contamination

    Wilcox Premium Sea Salt Caramel ice cream is being recalled for potential Listeria monocytogenes contamination. Affected products with best-by dates of 9/14/24 to 11/14/24 were distributed in VT, NH, MA, and NY.

    Product
    Wilcox Premium Sea Salt Caramel; 4 oz Cup; UPC 04372600404; Wilcox Premium Sea Salt Caramel in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0516-2024·2023-12-20

    Wilcox Ice Cream Recalls Maple Cream for Potential Listeria Contamination

    Wilcox Ice Cream is recalling Maple Cream in 1.5 quart and pint sizes due to potential Listeria monocytogenes contamination. The affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York with best-by dates from September 13 to November 14, 2024.

    Product
    Wilcox SUPER PREMIUM Maple Cream; 1.5 QT (UPC 04372601510) and Pint (UPC 04372601610)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0596-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. recalls Acorn Raspberry Creme Filled Cookies from gift baskets for undeclared tree nuts. Approximately 4,875 cookies across 1,168 gift boxes were distributed nationwide. Consumers with tree nut allergies should not consume this product.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #926 Tis The Season Bakery Gift Box
    Category
    Food
    Distribution
    50 states
  • CriticalFDA (Food)·F-0526-2024·2023-12-20

    Wilcox Ice Cream Bars Recalled Due to Listeria Contamination Risk

    Wilcox Ice Cream Bars (Espresso) sold in VT, NH, MA, and NY may be contaminated with Listeria monocytogenes. Consumers should not consume the product.

    Product
    Wilcox Ice Cream Bar (Dairy Based) - Espresso (UPC 043726005072)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0519-2024·2023-12-20

    Wilcox Super Java ice cream recalled due to Listeria contamination risk

    Wilcox SUPER PREMIUM Super Java ice cream (1.5 QT and Pint) may be contaminated with Listeria. Affected products were distributed in VT, NH, MA, and NY with Best By/Sell By dates from 9/13/24 to 11/14/24.

    Product
    Wilcox SUPER PREMIUM Super Java; 1.5 QT (UPC 04372601516) and Pint (UPC 04372601616)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0537-2024·2023-12-20

    Wilcox Premium Mint Chocolate Chip Ice Cream Recalled for Listeria Contamination

    Wilcox Premium Mint Chocolate Chip ice cream sold in VT, NH, MA, and NY has been recalled due to potential Listeria monocytogenes contamination. Consumers should discard the product or return it to the point of purchase.

    Product
    Wilcox Premium Mint Chocolate Chip in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0579-2024·2023-12-20

    Cantaloupe Recall: Salmonella Risk in Malichita Whole Cantaloupe

    PACIFIC TRELLIS FRUIT, LLC is recalling Malichita brand whole cantaloupes in 9-count and 12-count packages due to potential Salmonella contamination. The recall affects 4,872 cases distributed in Wisconsin, Oklahoma, Illinois, Texas, California, and Canada.

    Product
    Malichita brand Whole Cantaloupe 9 count and 12 count
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·F-0525-2024·2023-12-20

    Wilcox Ice Cream Bar Recalled for Potential Listeria Contamination

    Wilcox Ice Cream Bar (Black Raspberry) is being recalled due to potential Listeria monocytogenes contamination. The affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Ice Cream Bar (Dairy Based) Black Raspberry (UPC 043726005065)
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·F-0515-2024·2023-12-20

    Wilcox Ice Cream Chocolate Recalled Due to Listeria Contamination

    Wilcox SUPER PREMIUM Chocolate ice cream in 1.5 QT and Pint sizes is recalled for potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York with Best By/Sell By dates from 9/13/24 to 11/14/24.

    Product
    Wilcox SUPER PREMIUM Chocolate; 1.5 QT (UPC 04372601502) and Pint (UPC 04372601602)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0578-2024·2023-12-20

    Multiple fruit products recalled due to possible Salmonella contamination

    Vinyard Fruit & Vegetable Co. is recalling multiple fruit products distributed in Oklahoma due to possible Salmonella contamination. The recall includes Fruit Medley Cups, Cantaloupe Cubes, and Melon variety packs.

    Product
    Fruit Medley Cup 16/6 oz 3300-3 Cantaloupe Cube (2/5 lb) 3338-3 Fruit Mix Kit (4/5 lb) (Tray) 2963-3 3 Melon 16/6 oz cups 3330-3 Fruit Mix (2/5 lb) 3301-3 Cantaloupe Cube (5 lb) 3304-3 Cantaloupe Cubed 10/12 oz cups 0526-3 Melon Variety Pack 2964-3 3 Melon Medley 6 oz cups 2973-3
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0534-2024·2023-12-20

    Leonardo's Gelato Mint Chocolate Chip Recalled Due to Listeria Contamination

    Leonardo's Gelato Mint Chocolate Chip (pints and 4 oz cups) may be contaminated with Listeria monocytogenes. Products were distributed in VT, NH, MA, and NY with Best By dates from August 28–November 14, 2024.

    Product
    Leonardo's Gelato Mint Chocolate Chip; Pints (UPC 8 1643900050) and 4 oz cup (UPC 81643900041)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0531-2024·2023-12-20

    Leonardo's Gelato recalled due to possible Listeria monocytogenes contamination

    Leonardo's Gelato Sams Creamy Chocolate Chip products are being recalled due to possible Listeria monocytogenes contamination. The recall affects pints and 4 oz cups distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Leonardo's Gelato Sams Creamy Chocolate Chip; Pints (UPC 8 1643900019) and 4 oz cup (UPC 81643900040)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0546-2024·2023-12-20

    Wilcox Premium Fudge Ripple ice cream recalled for Listeria monocytogenes contamination

    Wilcox Premium Fudge Ripple ice cream is being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Premium Fudge Ripple in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0560-2024·2023-12-20

    Wilcox Premium Double Chocolate Ripple ice cream recalled for Listeria contamination

    Wilcox Premium Double Chocolate Ripple ice cream in multiple sizes is being recalled due to potential Listeria monocytogenes contamination. Consumers should discard or return affected products.

    Product
    Wilcox Premium Double Chocolate Ripple in 1.5QT, Quart, and Pint sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0521-2024·2023-12-20

    Wilcox Vanilla Yogurt Recalled Due to Listeria Contamination Risk

    Wilcox Vanilla Yogurt pints are recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in VT, NH, MA, and NY with Best By dates in October 2024.

    Product
    Wilcox Yogurt - Vanilla; Pint (UPC 04372600699)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0540-2024·2023-12-20

    Wilcox Premium Strawberry Ice Cream Recalled Due to Listeria Risk

    Wilcox Premium Strawberry ice cream in multiple sizes distributed in VT, NH, MA, and NY may contain Listeria monocytogenes. Consumers should discard affected products.

    Product
    Wilcox Premium Strawberry in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0522-2024·2023-12-20

    Wilcox Yogurt Recalled for Potential Listeria Monocytogenes Contamination

    Wilcox Yogurt - Maple Cream pints sold in Vermont, New Hampshire, Massachusetts, and New York are recalled due to potential Listeria monocytogenes contamination.

    Product
    Wilcox Yogurt - Maple Cream; Pint (UPC 04372600698)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0528-2024·2023-12-20

    Wilcox Ice Cream Bars Recalled for Potential Listeria Contamination

    Wilcox Ice Cream Bar in Maple Cream flavor is being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Ice Cream Bar (Dairy Based) Maple Cream; (UPC 043726005096)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0547-2024·2023-12-20

    Wilcox Premium Raspberry Cheesecake Ice Cream Recalled for Listeria Contamination

    Wilcox Premium Raspberry Cheesecake ice cream may be contaminated with Listeria monocytogenes. The recall affects products distributed in Vermont, New Hampshire, Massachusetts, and New York with best-by dates from 9/14/24 to 11/14/24.

    Product
    Wilcox Premium Raspberry Cheesecake in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0549-2024·2023-12-20

    Wilcox ice cream recall due to potential Listeria monocytogenes contamination

    Wilcox Premium Catamount Tracks ice cream sold in VT, NH, MA, and NY may be contaminated with Listeria monocytogenes. The Class I recall affects 19.31 tons with Best By dates from 9/14/24 to 11/14/24.

    Product
    Wilcox Premium Catamount Tracks in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0509-2024·2023-12-20

    Wilcox Premium Chocolate Ice Cream Recalled for Listeria Contamination

    Wilcox Premium Chocolate ice cream is recalled for potential Listeria monocytogenes contamination. Products with Best By dates 9/14/24–11/14/24 distributed in VT, NH, MA, and NY are affected.

    Product
    Wilcox Premium Chocolate; 4 oz Cup; UPC 04372600402; Wilcox Premium Chocolate in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0557-2024·2023-12-20

    Wilcox Premium Maple Cheesecake ice cream recalled for potential Listeria contamination

    Wilcox Ice Cream is recalling Wilcox Premium Maple Cheesecake due to potential Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Premium Maple Cheesecake in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0555-2024·2023-12-20

    Wilcox Premium Peppermint Ice Cream Recalled for Possible Listeria Contamination

    Wilcox Ice Cream is recalling Wilcox Premium Peppermint ice cream in multiple sizes distributed in Vermont, New Hampshire, Massachusetts, and New York due to possible Listeria monocytogenes contamination.

    Product
    Wilcox Premium Peppermint in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0548-2024·2023-12-20

    CereLink ICP Extension Cable Recalled for Out of Range Readings

    Integra LifeSciences is recalling CereLink ICP Extension Cables due to a design defect causing out of range readings. The Class I recall affects 4,941 units distributed nationwide and internationally.

    Product
    CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP) Monitor, Model No. 826820/826820P. Cable is also provided with monitor as part of the same SKU.
    Category
    Medical Device
    Distribution
    Distributed nationwide

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