The Recall Desk

State

Mississippi product recalls

20,083 recalls have nationwide distribution and so reach Mississippi. 0 additional recalls listed Mississippi specifically in their distribution scope.

About recalls in Mississippi

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Mississippi consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

5401–5425 of 20083

  • HighCPSC·25217·2025-04-10

    Modus Furniture Kentfield Dressers Recalled for Tip-Over and Entrapment Hazards

    Kentfield Solid Wood Eight-Drawer Dressers can tip over if not wall-anchored, risking entrapment injuries or death to children. Modus Furniture is offering free repair kits and installation.

    Product
    Kentfield Solid Wood Eight-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V769000·2025-04-10

    2022-2024 Suzuki GSX1300R motorcycles recalled for brake master cylinder defect

    Suzuki is recalling 2022-2024 GSX1300R motorcycles for a brake master cylinder defect that can reduce stopping power and increase crash risk. Dealers will replace the affected components at no cost.

    Product
    SUZUKI — 2024 SUZUKI GSX1300R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25222·2025-04-10

    Babyjoy High Chair Activity Centers Recalled for Entrapment and Fall Hazards

    Costway recalls about 1,400 Babyjoy Convertible 6-in-1 High Chair Activity Centers sold online at Walmart.com due to leg openings that can trap children and a tray that can disengage, posing entrapment and fall hazards.

    Product
    Babyjoy Convertible 6-in-1 High Chair Activity Centers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25215·2025-04-10

    Fisher-Price Brunch & Go Stroller Toys Recalled for Choking Hazard

    Fisher-Price is recalling about 253,000 Brunch & Go Stroller Toys because the egg component can crack and create choking hazards. No injuries have been reported; consumers should immediately stop use and request a free replacement.

    Product
    Brunch & Go Stroller Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25221·2025-04-10

    Multifunctional Puzzle Crab Toys with Magnets Recalled for Ingestion Hazard

    About 600 magnetic puzzle crab toys sold on Walmart.com are recalled because swallowed magnets can cause serious digestive injury. Consumers should stop using them immediately and request a full refund.

    Product
    Multifunctional Puzzle Crab Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1493-2025·2025-04-09

    VentStar Flex 220 Breathing Circuit Recalled for Potential Hose Cracks

    Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.

    Product
    Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1497-2025·2025-04-09

    Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks

    Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1498-2025·2025-04-09

    Anesthesia Circuit Kit Flex (P)2 recalled for potential breathing hose cracks

    Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is inten
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1495-2025·2025-04-09

    Draeger Anesthesia Circuit Kit Flex 1 recalled for potential hose cracks

    Draeger, Inc. is recalling Anesthesia Circuit Kit Flex 1 devices nationwide and internationally due to potential cracks in the breathing circuit hose that conducts anesthesia gases.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V574000·2025-04-09

    2025 Jeep Wagoneer S Incorrectly Installed Spring Disables Park Function

    Chrysler recalls 2024-2025 Jeep Wagoneer S and Dodge Charger electric vehicles due to an incorrectly installed spring that may disable the park function, potentially causing vehicle rollaway.

    Product
    JEEP — 2025 JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1496-2025·2025-04-09

    Anesthesia Circuit Kit Flex 2 recalled due to breathing hose crack risk

    Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1494-2025·2025-04-09

    Draeger ID Circuit Flex 220 breathing circuit hoses subject to cracking

    Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.

    Product
    Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1499-2025·2025-04-09

    Anesthesia Circuit Kit Flex EPA recalled due to breathing hose cracking

    Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intend
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1480-2025·2025-04-09

    Nasopore Nasal Dressing Recall Due to Compromised Sterile Packaging Seals

    Stryker Corporation is recalling Nasopore nasal dressings due to potentially compromised sterile packaging seals. Affected units totaling 182,344 may have lost sterility, posing a contamination risk.

    Product
    Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1481-2025·2025-04-09

    Nasopore Nasal Dressings Recalled Due to Breached Sterility Seals

    Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.

    Product
    Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1501-2025·2025-04-09

    Phoroptor VRx Digital Refraction System Recalled for Detachable Head

    Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.

    Product
    Phoroptor VRx Digital Refraction System Model Numbers: 16242
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V672000·2025-04-09

    2024 Harley-Davidson Motorcycles Recalled for Electrical Short Circuit Risk

    Harley-Davidson is recalling certain 2024 motorcycles because the voltage regulator output wire may rub on the crankcase, causing an electrical short circuit. This could result in loss of electrical and drive power while riding, increasing crash risk.

    Product
    HARLEY-DAVIDSON — 2024 HARLEY-DAVIDSON FLTRXSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1476-2025·2025-04-09

    Nasopore FD nasal dressing recalled for potential sterile barrier breach

    Stryker Corporation is recalling 182,344 units of Nasopore FD nasal dressing nationwide due to potentially breached sterile seals that may allow product contamination.

    Product
    Nasopore FD fragmentable nasal dressing, Catalog Numbers 5400-020-108 and 5400-020-108ITL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V657000·2025-04-09

    2023 Nissan Ariya Inverter Software May Cause Loss of Drive Power

    Nissan is recalling certain 2023 Ariya vehicles due to a potential inverter software defect that may cause an unexpected loss of drive power. The loss of drive power increases the risk of a crash.

    Product
    NISSAN — 2023 NISSAN ARIYA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V576000·2025-04-09

    Jeep Grand Cherokee Plug-In Hybrid Software Error Causes Loss of Drive Power

    Chrysler recalls certain 2022-2026 Jeep Grand Cherokee plug-in hybrids for a software error in the hybrid control processor that may cause loss of drive power and increase crash risk.

    Product
    JEEP — 2023 JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1474-2025·2025-04-09

    Nasopore nasal dressing recall: compromised sterile barrier seals

    Stryker recalls Nasopore 4cm fragmentable nasal dressings due to potential blister seal damage that compromises the sterile barrier. Nationwide distribution affected.

    Product
    Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25V577000·2025-04-09

    [pending] 2023 TOYOTA BZ4X

    Pending LLM rewrite. Source: NHTSA 25V577000.

    Product
    TOYOTA — 2023 TOYOTA BZ4X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V575000·2025-04-09

    [pending] 2025 JEEP WAGONEER S

    Pending LLM rewrite. Source: NHTSA 25V575000.

    Product
    JEEP — 2025 JEEP WAGONEER S
    Category
    Vehicle
    Distribution
    Distributed nationwide