The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

19726–19750 of 50413

  • HighNHTSA·21V599000·2021-08-02

    Software error may deactivate rear-view display in 2021 INFINITI Q60 vehicles

    A software error may disable the rear-view camera display in 2021 INFINITI Q60 vehicles, reducing rear visibility and increasing crash risk. Nissan will update the software at no cost.

    Product
    INFINITI — INFINITI Q50, QX80, Q60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V596000·2021-08-02

    2022 Mitsubishi Outlander seat belt retractor defect affects child restraints

    Mitsubishi is recalling certain 2022 Outlander vehicles due to seat belt retractors that may deactivate early, preventing child restraint systems from securing properly. Owners should contact MMNA at 1-888-648-7820 for free replacement.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V598000·2021-08-02

    2020 BMW X4 Engine Software Defect Disables Braking Assist

    BMW is recalling multiple 2020-2021 models, including the X4, due to engine management software that may disable braking assist. Owners should contact BMW at 1-800-525-7417 for a free software update.

    Product
    BMW — BMW, TOYOTA 745LE, X4, X3, M340I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V585000·2021-07-29

    Mitsubishi Fuso Recalls FEC9T Trucks for Loose Front Leaf Spring Bolts

    Mitsubishi Fuso is recalling 2020-2021 FEC9T trucks because loose front leaf spring shackle bolts may detach, creating a road hazard and increasing crash risk.

    Product
    MITSUBISHI FUSO — MITSUBISHI FUSO FEC9T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21770·2021-07-29

    Specialized Electric Mountain Bike Battery Packs Recalled for Fire and Burn Hazards

    Specialized is recalling about 2,500 first-generation Turbo Levo and Kenevo electric mountain bike battery packs because water can penetrate the seal around the LED control pad and cause the battery to short circuit, creating fire and burn hazards.

    Product
    Specialized 1st Generation Turbo Levo and Kenevo electric mountain bike battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V583000·2021-07-29

    NRC Recalls 2019-2020 Motorhomes Due to Gas Leak Risk

    NRC is recalling 2019-2020 motorhomes because an overtightened stove bolt may damage the seal, causing a gas leak that increases fire risk.

    Product
    NRC — NRC MOTOR HOME
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V578000·2021-07-29

    2020-2021 Silverado 2500 and Sierra 2500 Spare Tire ABS Failure Recall

    General Motors is recalling 2020-2021 Silverado 2500 and Sierra 2500 trucks where a 17-inch spare tire paired with larger road tires prevents ABS from engaging, raising crash risk. Dealers will replace the spare tire and label at no cost.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 2500, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V584000·2021-07-29

    Land Rover Defender Recall for Incorrect Child Seat Manual Information

    Jaguar Land Rover is recalling 2020-2021 Defender vehicles because the owner's manual incorrectly states that third-row seats have LATCH top tethers, which may lead to improper child seat installation.

    Product
    LAND ROVER — LAND ROVER DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21769·2021-07-29

    Children's Sleepwear Sets Recalled for Flammability Standard Violation

    SHEIN children's sleepwear sets fail to meet federal flammability standards and pose a burn injury risk. About 2,320 units sold online from August 2019 through January 2021 are affected.

    Product
    Children's Sleepwear Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V589000·2021-07-29

    Spartan RV Chassis Instrument Cluster May Intermittently Go Blank

    Shyft Group is recalling certain 2018-2022 Spartan RV Chassis models (K1, K2, K3, K4) because the instrument cluster may intermittently go blank while the vehicle is in motion, potentially obscuring critical speed and warning information.

    Product
    SPARTAN — SPARTAN K2, K4, K3, K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2117-2021·2021-07-28

    Exactech Connexion GXL Hip Implant Liners Recalled for Premature Wear Risk

    Exactech is recalling 89,050 Connexion GXL acetabular hip implant liners due to a risk of edge-loading and premature wear in certain implant configurations. No illnesses or injuries have been reported.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 130-32-XX, Acumatch GXL 0 Degree Liner, 32mm; and Novation GXL Liner, Neutral, 32mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2095-2021·2021-07-28

    Infant Heel Warmer Recalled Due to Risk of Rupture and Contents Splashing

    Cardinal Health is recalling 2.9 million infant heel warmers that may rupture or leak during activation, potentially splashing heated contents onto infants' eyes or skin and causing rash, burn, or inflammation.

    Product
    Infant Heel Warmer without Attachment Tab, Nonsterile, Active Product SKU MH00002N The infant heel warmer is activated at the point of care by squeezing the pouch. This mixes the substrates inside the pouch causing an exothermic chemical reaction, warming the pouch, which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2116-2021·2021-07-28

    Hip Implant Acetabular Liners Recalled for Premature Wear Risk

    Exactech Connexion GXL acetabular polyethylene liners used in orthopedic hip implants are recalled due to risk of edge-loading and premature wear in certain configurations. The recall affects 89,050 units distributed nationwide.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 130-28-XX, Acumatch GXL 0 Degree Liner, 28mm; Novation GXL Liner, Neutral, 28mm; and Novation GXL Neutral Liner, G0, 28mm ID. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21171·2021-07-28

    Children's Pajamas Recalled for Flammability Standard Violation

    Tkala Fashion children's pajamas fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 6,000 units sold on Amazon from January through June 2021 are affected.

    Product
    Children's Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2096-2021·2021-07-28

    Mediana Vital Signs Monitor May Fail to Power Up or Respond

    Mediana AVSM3 SNF vital signs monitors may fail to power up or have unresponsive button controls, potentially preventing patient vital sign monitoring. The company is recalling 618 units distributed in Wisconsin.

    Product
    AVSM3 SNF, Vital Signs Monitor The monitor is intended to be used to monitor noninvasive blood pressure (NIBP), functional arterial oxygen saturation (SpO2), pulse rate (PR), temperature (Temp) for adult, pediatric and neonatal patients in all areas of a hospital and…
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2097-2021·2021-07-28

    Medical Device Recall: Illuminated Laser Probe with Incorrect Expiration Date

    Dutch Ophthalmic USA is recalling 13 boxes of Illuminated Stepped Laser Probe Curved devices due to a barcode labeling error. The barcode displays 2025-10-27 when the correct expiration date is 2024-10-01.

    Product
    Illuminated Stepped Laser Probe Curved-for use in combination with 23G vitrectomy system Product Code: 7510.ALC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2126-2021·2021-07-28

    Exactech GXL Hip Implant Liners Recalled for Premature Wear Risk

    Exactech is recalling its Connexion GXL acetabular polyethylene liners used in hip implants because they may experience edge-loading and premature wear in certain patient configurations and surgical positioning. A total of 89,050 units were distributed nationwide.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 136-28-XX, Novation GXL Liner, +5mm Lateralized, 28mm; and Novation GXL Liner, +5mm Lateralized, G0, 22mm ID. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2132-2021·2021-07-28

    Exactech Hip Implant Liners Recalled Due to Premature Wear Risk

    Exactech is recalling Connexion GXL hip implant liners due to edge-loading and premature wear risk in certain patient configurations. The recall affects 89,050 units distributed nationwide.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 138-32-XX, Novation GXL Liner, 10 Deg Face, 32mm. Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 138-36-XX, Acumatch…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2124-2021·2021-07-28

    Hip implant liners recalled for edge-loading and premature wear

    Exactech Connexion GXL hip implant liners are recalled due to risk of edge-loading and premature wear in certain configurations. About 89,050 units distributed nationwide are affected.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 134-28-XX, Acumatch GXL, Ext Cov Liner, 28mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2021·2021-07-28

    Exactech Connexion GXL Hip Implant Liners Recalled for Premature Wear Risk

    Exactech recalls approximately 89,050 Connexion GXL acetabular polyethylene hip implant liners due to risk of edge-loading and premature wear in certain implant configurations.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-40-XX, Novation GXL Liner, Lipped Ant, 40mm; Novation GXL Liner, Lipped, 40mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2128-2021·2021-07-28

    Hip Implant Liners Recalled Due to Premature Wear Risk

    Exactech Connexion GXL acetabular polyethylene liners used in hip replacement systems are recalled due to risk of edge-loading and premature wear in certain patients. The 89,050 affected units were distributed nationwide.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 136-36-XX, Novation GXL Liner, +5mm Lateralized, 36mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0784-2021·2021-07-28

    Pow Pow Powders Vanilla Chai Powder Recalled for Undeclared Milk Allergen

    San Diego Coffee, Tea and Spice is recalling Pow Pow Powders Vanilla Chai because the product lacks ingredient and allergen labeling, leaving milk allergen undeclared. The recall affects smoothie mixes distributed in California.

    Product
    Pow Pow Powders: A standard of Quality Vanilla Chai; NET Wt. 3.50 lb. (1.59kg) Ingredients: Sugar, Non-Fat Dry Milk, Non-Dairy Creamer (coconut oil, Corn Syrup Solids, Sodium Caseinate (a milk derivative), Sodium Citrate, Mono and Diglycerides, Salt), Instant Black Tea…
    Category
    Food
    Distribution
    1 state