The Recall Desk

Archive

December 2023 recalls

600 recalls were announced in December 2023.

What the numbers show

Critical
29
Severe
213
High
307
Moderate
49
Low
2

Of the 600 recalls this month scored against our rubric, 5% are Critical, 36% are Severe.

101–200 of 600

  • HighFDA (Drugs)·D-0157-2024·2023-12-27

    Nystatin Bulk Powder Recall for Incorrect Label Assay Value

    Fagron, Inc. is recalling Nystatin 150 MU bulk powder for prescription compounding because the assay value on the label is incorrect.

    Product
    NYSTATIN 150 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 51552-0041-1, Bar code 3 51552 00411 5
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-0607-2024·2023-12-27

    RAPIDPoint 500 Diagnostic Cartridges Recall Due to Sodium Sensor Measurement Bias

    Siemens is recalling RAPIDPoint 500 measurement cartridges because the sodium sensor can produce inaccurate readings, potentially leading to delayed diagnosis or incorrect treatment of electrolyte imbalances.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 250-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491447
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0573-2024·2023-12-27

    Injection Needles Recalled for Inadequate Manual Cleaning Process

    Karl Storz is recalling 1,127 injection needles used in general and visceral surgery because the manual cleaning process cannot be adequately assured, potentially increasing infection risk for patients.

    Product
    Injection Needle, LUER-lock,0.8mm, REF: 26175PD
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0605-2024·2023-12-27

    Venous probe connection cable defects in Cardiohelp-i extracorporeal support systems

    Maquet Medical Systems USA is recalling venous probe connection cables for the Cardiohelp-i System due to insulation and wire breaks. Defective cables may prevent the system from receiving critical blood flow and temperature information.

    Product
    Venous probe connection cable (REF 701069333 and 701048804) used with the Cardiohelp-i System, part numbers 701072780 and 701041802
    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…
    Category
    Food
    Distribution
    12 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-0574-2024·2023-12-27

    Injection needles recalled due to cleaning efficacy concerns

    Karl Storz Endoscopy is recalling injection needles used in general and visceral surgery due to concerns that the manual cleaning process cannot ensure adequate sterilization, which may increase infection risk.

    Product
    Injection Needle, single cvd. 70 degrees, REF: 738750; Injection Needle, single cvd. 80 degrees, REF: 738752; Injection Needle, bayonet, 13 cm, REF: 738756; Injection Needle, angular, 13 cm, REF: 738758; Needle, bayonet-shaped, REF: 810505; Needle, Septum, angular, REF: 810506
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-0604-2024·2023-12-27

    Shakespeare's Pizza frozen pizza recalled for undeclared wheat

    Shakespeare's Pizza is recalling 18,712 frozen pizzas due to undeclared wheat. The product was sold in retail stores in Missouri and Kansas and through online sales; consumers with wheat allergies should not consume it.

    Product
    Shakespeare's Pizza, Extra Cheese Pizza, 25 oz, Keep Frozen; UPC 686 148 007 370; pack size 20 per case.
    Category
    Food
    Distribution
    2 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-0572-2024·2023-12-27

    Injection needles and cannulas recalled for cleaning process efficacy issues

    Karl Storz Endoscopy is recalling injection needles and cannulas because the manual cleaning process may not effectively remove contaminants, potentially exposing patients to infection risk.

    Product
    Injection Needle, 3 Fr., REF: 27030N; Injection Cannula, 6 Fr., REF: 27182A
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Devices)·Z-0588-2024·2023-12-27

    Exactech Vantage Mobile Bearing Tibial Inserts Recalled Due to Vacuum Loss

    Exactech is recalling Vantage Mobile Bearing Tibial Inserts due to loss of vacuum in the innermost vacuum bag. Three complaints involving four devices have been reported.

    Product
    Exactech Vantage Mobile Bearing Tibial Inserts, Catalog Numbers: a) 350-41-23, b) 350-42-03
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0584-2024·2023-12-27

    Exactech Optetrak Logic PS Knee System Vacuum Loss Recall

    Exactech is recalling certain Optetrak Logic PS Knee Systems due to potential loss of vacuum in the inner-most vacuum bag. The company has received 3 complaints involving 4 devices.

    Product
    Exactech Optetrak Logic PS Knee System, Catalog Numbers: 02-012-35-5009
    Category
    Medical Device
    Distribution
    16 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-0571-2024·2023-12-27

    Injection Needle Recall Due to Cleaning Process Concerns

    Karl Storz Endoscopy is recalling injection needles used in general and visceral surgery because the manual cleaning process cannot be assured effective, which may expose patients to a higher risk of infection.

    Product
    Injection Needle, REF: 25207
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-0605-2024·2023-12-27

    Frozen pizza recalled for undeclared wheat allergen

    Shakespeare's Pizza recalls Four Cheese Pizza due to undeclared wheat allergen. The product was distributed in Missouri, Kansas, and through online sales.

    Product
    Shakespeare's Pizza, Four Cheese Pizza, 25 oz, Keep Frozen; UPC 686 148 000 050; pack size 20 per case.
    Category
    Food
    Distribution
    2 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-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-0578-2024·2023-12-27

    Hip Implant Liner Recalled Due to Loss of Vacuum in Inner Bag

    Exactech has recalled certain Alteon Hip XLE Liner hip implant components due to vacuum loss in the inner vacuum bag. The company has received 3 complaints involving 4 devices related to this issue.

    Product
    Exactech Alteon Hip XLE Liner, Catalog Numbers: a) 01-030-40-0636, b) 01-030-40-0640, c) 01-030-42-0536
    Category
    Medical Device
    Distribution
    16 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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
  • 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-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)…
    Category
    Medical Device
    Distribution
    16 states
  • 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-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…
    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-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
  • 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·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
  • 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·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 XE35, XE40, XE60
    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·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
  • 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·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
  • 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·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·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 TRANSCONTINENTAL, R 18 B
    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·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
  • 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·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·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·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
    WHEELED COACH — WHEELED COACH, ROAD RESCUE, REV AMBULANCE TYPE III, TYPE IX, 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
  • 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·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 450, AMG GLE63, AMG E63, E 350
    Category
    Vehicle
    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·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
  • 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
  • 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
  • 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
  • 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·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
  • 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
  • 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
  • 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-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-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-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-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-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-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-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-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-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
  • 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-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-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-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
  • SevereFDA (Food)·F-0508-2024·2023-12-20

    Wilcox Premium Vanilla Ice Cream Recalled Due to Listeria Contamination Risk

    Wilcox Premium Vanilla ice cream in multiple sizes may be contaminated with Listeria monocytogenes. Products distributed in Vermont, New Hampshire, Massachusetts, and New York with Best By dates from September to November 2024 are affected.

    Product
    Wilcox Premium Vanilla; 4 oz Cup; UPC 0437260401; Wilcox Premium Vanilla in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0591-2024·2023-12-20

    Acorn Raspberry Cookies Recalled for Undeclared Tree Nut Allergen

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies sold in gift baskets due to undeclared tree nuts. Consumers with tree nut allergies should not consume the product.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #342 Bakery Bonanza
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0595-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies found in gift basket #925 due to undeclared tree nuts. The product poses a health risk to consumers with tree nut allergies.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #925 Bakery, Coffee & Cocoa Gift Collection
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0561-2024·2023-12-20

    Wilcox Premium Sweet Cream recalled for potential Listeria contamination

    Wilcox Premium Sweet Cream in multiple sizes with Best By dates 9/14/24 to 11/14/24 is being recalled due to potential Listeria monocytogenes contamination. Products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Wilcox Premium Sweet Cream in 1.5QT, Quart, and Pint sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0533-2024·2023-12-20

    Gelato product recalled due to potential Listeria contamination

    Leonardo's Gelato Hazelnut Gelato (sold 8/28/24–11/14/24) may be contaminated with Listeria monocytogenes. Consumers should not eat affected products and contact the manufacturer.

    Product
    Leonardo's Gelato Hazelnut Gelato; Pints (UPC 04372601703)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0505-2024·2023-12-20

    Philips Panorama MR System Structural Failure Risk from Helium Gas Pressure

    Philips Panorama 1.0T MR Systems (Models 781250, 781350) may experience structural failure during helium quench events, releasing pressurized gas and debris that could cause helium exposure, asphyxia, and injury to patients and operators.

    Product
    Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical Electrical Systems for use as a diagnostic device.
    Category
    Medical Device
    Distribution
    34 states
  • SevereFDA (Food)·F-0582-2024·2023-12-20

    Cut Cantaloupe Products Recalled for Salmonella Contamination

    Cut Fruit Express, Inc. is recalling multiple cut cantaloupe products distributed in Illinois, Minnesota, and Wisconsin due to potential Salmonella contamination. Consumers should not consume the affected products.

    Product
    Cut cantaloupe identified with the following Item ID and Description. 1. 11628 Cantaloupe Diced 3/4" 5lb. 2. 13075 Cantaloupe Chunk 30-1/2 cup 3. 1460070 Cantaloupe Chunk 1" 5lb. 4. 4384418 Cantaloupe Chunk 25lb. Pail. 5. 4586 Cantaloupe Chunks 16oz. 6.…
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0536-2024·2023-12-20

    Wilcox Premium Cookies in Cream ice cream recalled for Listeria

    Wilcox Premium Cookies in Cream ice cream in multiple sizes is being recalled due to possible Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York with best-by dates between September 14 and November 14, 2024.

    Product
    Wilcox Premium Cookies in Cream in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0514-2024·2023-12-20

    Ice Cream Recalled Due to Possible Listeria Contamination

    Wilcox SUPER PREMIUM Salted Caramel Brownie ice cream may be contaminated with Listeria monocytogenes. The recall affects products sold in Vermont, New Hampshire, Massachusetts, and New York with best-by dates from September 13 to November 14, 2024.

    Product
    Wilcox SUPER PREMIUM Salted Caramel Brownie; 1.5 QT (UPC 04372601520) and Pint (UPC 04372601620)
    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-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-0535-2024·2023-12-20

    Leonardo's Gelato Maple Flavor Recalled for Possible Listeria Contamination

    WILCOX ICE CREAM is recalling Leonardo's Gelato VT Maple Gelato 4 oz cups due to possible Listeria monocytogenes contamination. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York.

    Product
    Leonardo's Gelato VT Maple Gelato; 4 oz Cup (UPC 81643900056)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0542-2024·2023-12-20

    Wilcox Premium Chocolate Chip Ice Cream Recalled Due to Listeria Contamination

    Wilcox Premium Chocolate Chip ice cream is being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in VT, NH, MA, and NY with best-by dates from September 14 to November 14, 2024.

    Product
    Wilcox Premium Chocolate Chip in 1.5QT, Quart, Pint, and 3 Gallon sizes
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0529-2024·2023-12-20

    Wilcox Ice Cream Bars recalled for potential Listeria contamination

    Wilcox Ice Cream Bar (Pumpkin) products may be contaminated with Listeria monocytogenes. Affected products were distributed in Vermont, New Hampshire, Massachusetts, and New York with best-by dates from September 15 to November 14, 2024.

    Product
    Wilcox Ice Cream Bar (Dairy Based) Pumpkin ; (UPC 043726005010)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0597-2024·2023-12-20

    Acorn Raspberry Creme Filled Cookie Recall Due to Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in gift basket #927 due to undeclared tree nut allergen. The cookies were distributed nationwide.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #927 Fresh Baked Cookie, Brownie and Cake Collection
    Category
    Food
    Distribution
    50 states
  • SevereFDA (Food)·F-0590-2024·2023-12-20

    Acorn Raspberry Creme Cookies Recalled for Undeclared Tree Nuts

    Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies distributed nationwide in gift baskets due to undeclared tree nuts. Consumers with tree nut allergies face risk of allergic reaction.

    Product
    Acorn Raspberry Creme Filled Cookie found in gift basket: #197 Gourmet Bakery Basket
    Category
    Food
    Distribution
    50 states

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