The Recall Desk

State

Mississippi product recalls

73,509 recalls have nationwide distribution and so reach Mississippi. 5,379 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total
5,379
Critical
933
Severe
1,347
Most recent
2026-10-24

Of the 5,379 recalls naming Mississippi we have scored against our rubric, 933 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,347 (25%) are Severe.

These figures cover only the 5,379 recalls whose distribution notice names Mississippi specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23776–23800 of 78888

  • HighNHTSA·22V029000·2022-01-25

    Forest River Recalls Transit Buses Due to Fire Risk from Relay Module

    Forest River is recalling specific 2021-2023 transit buses because a failed relay module can increase the risk of a fire. Dealers will install a wire jumper harness free of charge.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS, STARCRAFT BUS COMMUTE, SENATOR II HD, ALLSTAR XLT, ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V030000·2022-01-25

    2021 Harley-Davidson Motorcycles Instrument Cluster May Fail in Cold Weather

    Certain 2021 Harley-Davidson motorcycles may not display the speedometer or neutral indicator at startup in freezing temperatures, creating a crash risk. Owners should contact Harley-Davidson for a free software update.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON RH1250S, RA1250S, RA1250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V031000·2022-01-25

    Kia Recalls Vehicles Due to Potential Air Bag Deactivation

    Kia is recalling specific 2017-2019 models because a defect may prevent air bags from deploying in a crash.

    Product
    KIA — KIA FORTE KOUP, SOUL EV, SEDONA, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V028000·2022-01-24

    Inland Empire Trailers Recalls 2021 Models Due to Axle Spindle Nut Issues

    Inland Empire Trailers is recalling 50 units of 2021 trailers because improperly tightened axle spindle nuts may cause overheating and loss of control.

    Product
    INLAND EMPIRE TRAILERS — INLAND EMPIRE TRAILERS CUSTOM TRAILER, UTILITY/ DUMP TRAILER, FLAT DECK TRAILER, ENCLOSED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V027000·2022-01-24

    2022 Mitsubishi Outlander Recalled for Defective Fuel Pump

    Mitsubishi is recalling certain 2022 Outlander vehicles because the fuel pump may fail due to incorrectly fused internal components. Fuel pump failure can cause engine stall, increasing the risk of a crash.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V023000·2022-01-21

    BMW Recalls 2019-2020 K 1600 Motorcycles for Rear Suspension Defect

    BMW is recalling 2019-2020 K 1600 GT, GTL, and B motorcycles because a rear suspension link strut may be insufficiently strong, potentially affecting stability and increasing crash risk.

    Product
    BMW — BMW K 1600 GTL, K 1600 GT, K 1600 B
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V025000·2022-01-21

    Rosenbauer Fire Trucks Recalled for Rear Axle Drive Pinion Fracture Risk

    Rosenbauer America is recalling 127 Commander, Warrior, and Avenger vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, WARRIOR, AVENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V022000·2022-01-21

    Kia Recalls 2020 Cadenza for Rear Power Window Safety Issue

    Kia is recalling 2020 Cadenza vehicles because rear power windows can operate after the ignition is off, increasing injury risk.

    Product
    KIA — KIA CADENZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V026000·2022-01-21

    Trails West Recalls 2017-2021 Trailers Due to Propane Regulator Fire Risk

    Trails West is recalling 2017-2021 Sierra, Classic, Santa Fe, and Freeride trailers because a propane regulator may fail, increasing fire risk.

    Product
    TRAILS WEST — TRAILS WEST SIERRA, FREERIDE, CLASSIC, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E003000·2022-01-20

    Pacific Trailer Recalls RAM A Frame Couplers Due to Welding Defect

    Pacific Trailer is recalling RAM A Frame 2 5/16" couplers because improper welding may cause the trailer to separate from the tow vehicle.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V019000·2022-01-20

    Spartan Fire Vehicles Recalled for Rear Axle Drive Pinion Fracture Risk

    Marion Body Works is recalling 2021-2022 Spartan Fire vehicles because a rear axle drive pinion may fracture, potentially engaging the parking brake without warning and increasing crash risk.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V018000·2022-01-20

    2021-2022 Heartland RVs Recalled for Tire Belt Separation Risk

    Certain 2021-2022 Heartland Cyclone, Fuel, Gravity, and Road Warrior vehicles with Sailun tires may experience belt separation, risking loss of vehicle control. Dealers will replace affected tires at no cost.

    Product
    HEARTLAND — HEARTLAND CYCLONE, GRAVITY, FUEL, ROAD WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0371-2022·2022-01-19

    Teva Norepinephrine Bitartrate Injection Recalled for Sterility Assurance

    Teva Pharmaceuticals is recalling Norepinephrine Bitartrate Injection USP due to lack of assurance of sterility. The affected lot is distributed in Tennessee, Mississippi, and Ohio.

    Product
    Norepinephrine Bitartrate Injection USP 4 mg/4 mL (1 mg/mL), 4 mL Single-Dose Vials, 10 vials per carton, Rx Only, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 0703-1153-03.
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Food)·F-0386-2022·2022-01-19

    Dream Pops Birthday Cake Bites Recalled for Undeclared Milk Allergen

    Dream Pops 100% Plant-Based Birthday Cake Bites are being recalled because they contain undeclared milk, a known allergen that poses a risk to people with milk allergies.

    Product
    100% Plant-Based Dream Pops Birthday Cake Bites UPC 854097008339
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0387-2022·2022-01-19

    Dream Pops Cookie Dough Bites Recalled for Undeclared Milk Allergen

    Dream Pops 100% Plant-Based Cookie Dough Bites are being recalled because they contain undeclared milk allergen. The product was distributed nationwide in the US and Canada.

    Product
    100% Plant-Based Dream Pops Cookie Dough Bites UPC 854097008322
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0369-2022·2022-01-19

    Exela Sodium Bicarbonate Injection Recalled for Sterility Assurance Failure

    Exela Pharma Sciences is recalling 8.4% Sodium Bicarbonate Injection due to lack of assurance of sterility. The affected lot (C0001088/P0001317, expiring 08/2023) was distributed nationwide.

    Product
    8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL), 50 mL vials, Rx Only, Manufactured and Distributed by: Exela Pharma Sciences, LLC., Lenoir, NC 28645, NDC 51754-5001-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0370-2022·2022-01-19

    Methylprednisolone Acetate Injectable Suspension Lacks Sterility Assurance

    Teva Pharmaceuticals is recalling Methylprednisolone Acetate Injectable Suspension 400 mg/10mL due to lack of assurance of sterility. The recall affects one lot distributed to facilities in Tennessee, Mississippi, and Ohio.

    Product
    MethylPREDNISolone Acetate Injectable Suspension USP 400 mg/10mL (40mg/mL), 10 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN 38141, Manufactured By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, NDC 16714-090-01, packaged in cartons.
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0375-2022·2022-01-19

    Clobetasol Propionate Ointment Recalled for Microbial Contamination

    Taro Pharmaceuticals is recalling Clobetasol Propionate Ointment USP 0.05% due to the presence of R. Pickettii bacteria in a non-sterile product. The affected lot may have been distributed nationwide through retailers.

    Product
    CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0468-2022·2022-01-19

    Maquet Sevoflurane vaporizer filling recalled due to potential hydrogen fluoride exposure

    Getinge Usa Sales Inc recalls Vaporizer Sevoflurane components in anesthesia systems due to potential chemical degradation that may cause hydrogen fluoride exposure via inhalation or skin contact.

    Product
    Vaporizer Sevoflurane Maquet Filling, Part No. 6886601 Component of the following systems: Product Code(s) UPN/UDI: Flow-c Anesthesia System 6887700 07325710009765 Flow-e Anesthesia System 6887900 07325710010457 Flow-i Anesthesia System C20 6888520 07325710010617 Flow-i…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0384-2022·2022-01-19

    Dream Pops Vanilla Sky Bites Recalled for Undeclared Milk Allergen

    Dream Pops 100% Plant-Based Vanilla Sky Bites are being recalled because they contain undeclared milk, a common allergen that may pose a health risk to consumers with milk allergies.

    Product
    100% Plant-Based Dream Pops Vanilla Sky Bites UPC 854097008254
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0385-2022·2022-01-19

    Dream Pops Berry Dreams Bites Recalled for Undeclared Milk Allergen

    Dream Pops is recalling 100% Plant-Based Dream Pops Berry Dreams Bites due to undeclared milk allergen. The product was distributed nationwide in the US and Canada with Best By dates from 6/28/22 to 10/21/22.

    Product
    100% Plant-Based Dream Pops Berry Dreams Bites UPC 854097008247
    Category
    Food
    Distribution
    Distributed nationwide