The Recall Desk

State

Michigan product recalls

19,702 recalls have nationwide distribution and so reach Michigan. 0 additional recalls listed Michigan specifically in their distribution scope.

About recalls in Michigan

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 Michigan 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.

476–500 of 19702

  • HighFDA (Devices)·Z-2258-2026·2026-06-03

    [pending] Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M

    Pending LLM rewrite. Source: FDA_DEVICE Z-2258-2026.

    Product
    Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2233-2026·2026-06-03

    [pending] Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINA

    Pending LLM rewrite. Source: FDA_DEVICE Z-2233-2026.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0245; 2) SPINAL TRAY W/PENCIL POINT NDL, Medline Kit SKU DYNJRA0555; 3) SPINAL TRAY, Medline Kit SKU DYNJRA0836A; 4) SPINAL T
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2237-2026·2026-06-03

    [pending] Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL

    Pending LLM rewrite. Source: FDA_DEVICE Z-2237-2026.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL ANESTHESIA TRAY-LF, Medline Kit SKU DYNJRA0102A; 2) SPINAL TRAY-LF, Medline Kit SKU DYNJRA0143B; 3) SPINAL PREP TRAY-LF, Medline Kit SKU DYNJRA0205B; 4) SPINAL TRAY, Medline Ki
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0551-2026·2026-06-03

    [pending] PRED MILD (PREDNISOLONE ACETATE)

    Pending LLM rewrite. Source: FDA_DRUG D-0551-2026.

    Product
    PRED MILD — PRED MILD (PREDNISOLONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2236-2026·2026-06-03

    [pending] Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPI

    Pending LLM rewrite. Source: FDA_DEVICE Z-2236-2026.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) SPINAL BLOCK TRAY, Medline Kit SKU DYNJRA1097; 2) TRAY, SPINAL PENCIL POINT 25G, Medline Kit SKU DYNJRA1154; 3) SPINAL TRAY, Medline Kit SKU DYNJRA1192A; 4) BLOCK TRAY, Medline
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2238-2026·2026-06-03

    [pending] Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Cod

    Pending LLM rewrite. Source: FDA_DEVICE Z-2238-2026.

    Product
    Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged, UK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V068000·2026-06-02

    [pending] 2025 HYUNDAI IONIQ 5

    Pending LLM rewrite. Source: NHTSA 26V068000.

    Product
    HYUNDAI — 2025 HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V070000·2026-06-02

    [pending] 2020 MERCEDES-BENZ METRIS

    Pending LLM rewrite. Source: NHTSA 26V070000.

    Product
    MERCEDES-BENZ — 2020 MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V069000·2026-06-02

    2026 Hyundai Kona vehicles recalled for front steering knuckle defect

    Hyundai is recalling certain 2026 Kona vehicles because the front steering knuckles may crack and break due to a manufacturing error, which can cause loss of steering control and increase crash risk.

    Product
    HYUNDAI — 2026 HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V102000·2026-06-02

    [pending] 2025 VOLVO VNR (4)

    Pending LLM rewrite. Source: NHTSA 25V102000.

    Product
    VOLVO — 2025 VOLVO VNR (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V073000·2026-06-02

    [pending] 2022 MERCEDES-BENZ EQB 300 4MATIC

    Pending LLM rewrite. Source: NHTSA 26V073000.

    Product
    MERCEDES-BENZ — 2022 MERCEDES-BENZ EQB 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V053000·2026-06-01

    [pending] 2024 NISSAN MURANO

    Pending LLM rewrite. Source: NHTSA 24V053000.

    Product
    NISSAN — 2024 NISSAN MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V054000·2026-06-01

    [pending] 2022 WINNEBAGO MICRO MINNIE FLX

    Pending LLM rewrite. Source: NHTSA 24V054000.

    Product
    WINNEBAGO — 2022 WINNEBAGO MICRO MINNIE FLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V051000·2026-06-01

    [pending] 2020 TESLA MODEL 3

    Pending LLM rewrite. Source: NHTSA 24V051000.

    Product
    TESLA — 2020 TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V052000·2026-06-01

    [pending] 2023 SPARTAN K2

    Pending LLM rewrite. Source: NHTSA 24V052000.

    Product
    SPARTAN — 2023 SPARTAN K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26508·2026-05-28

    MiniWarGaming and Primal Horizon Disc Magnets Violate Mandatory Safety Standard

    MiniWarGaming Inc. and Primal Horizon are recalling approximately 22,624 disc magnets that violate mandatory safety standards. The high-powered magnets pose a deadly ingestion hazard to children.

    Product
    MiniWarGaming and Primal Horizon Disc Magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26515·2026-05-28

    Anzmtosn Luminous Fidget Spinner Balls Recalled for Battery Ingestion Risk

    Anzmtosn Luminous Fidget Spinner Balls are recalled because the included mini flashlight contains easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children.

    Product
    Anzmtosn Luminous Fidget Spinner Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26514·2026-05-28

    Misco Sports Light-Up Racket Sets Recalled for Battery Ingestion Risk

    Missry Associates recalls Misco Sports Light-Up Racket Sets (model MT2287) because the battery compartment screw can detach and button cell batteries in the shuttlecock can be easily accessed by children, posing risk of serious injury or death if swallowed.

    Product
    Misco Sports Light-Up Racket Sets, model MT2287
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26512·2026-05-28

    Giantex Outdoor Lounge Chairs Recalled Due to Amputation Hazard

    Giantex outdoor lounge chairs model NP10025NY pose an amputation risk when adjusting the backrest due to exposed pinch points. One finger amputation has been reported.

    Product
    Giantex outdoor lounge chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26513·2026-05-28

    Joy Furniture Recalls Talan and Royce Living Room Furniture Sets

    Joy Furniture is recalling about 10,400 Talan and Royce sofas, loveseats, and recliners due to a fire hazard in the power switch that can overheat. The firm has reported 41 incidents including smoking, burning, and two fires, with no injuries reported so far.

    Product
    Talan and Royce Collection Sofas, Loveseats and Recliners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26522·2026-05-28

    Walmart recalls Mainstays 9-drawer fabric dressers due to tip-over hazard

    Walmart is recalling about 165,000 Mainstays 9-Drawer Fabric Dressers because they can tip over and cause entrapment if not anchored to a wall, creating a risk of serious injury or death to children.

    Product
    Mainstays 9-Drawer Fabric Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26506·2026-05-28

    Giantex and Costway Portable Steam Saunas Recalled for Burn Hazard

    Giantex and Costway portable steam saunas are recalled because the steam diffuser can position too close to the user's body, causing burns. Giantex has received nine burn reports, including one second-degree burn.

    Product
    Giantex and Costway 2-liter and 3-liter Portable Steam Saunas
    Category
    Consumer Product
    Distribution
    Distributed nationwide