The Recall Desk

State

Minnesota product recalls

20,096 recalls have nationwide distribution and so reach Minnesota. 0 additional recalls listed Minnesota specifically in their distribution scope.

About recalls in Minnesota

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 Minnesota 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.

7826–7850 of 20096

  • ModerateFDA (Devices)·Z-2811-2024·2024-09-04

    BVI CustomEyes Procedure Packs recalled for syringe manufacturing defect

    Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The affected procedure packs contain low dead space Luer Lock and Luer Slip 1ml syringes distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000501;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2819-2024·2024-09-04

    Beaver Visitec Recalls Medical Device Syringes in CustomEyes Procedure Packs

    Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs because they contain defective syringes manufactured by Sol-M. The 237 affected units were distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000711;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2910-2024·2024-09-04

    BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled

    Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing 1ml syringes manufactured by Sol-Millennium Medical, Inc., distributed nationwide in the United States.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001753;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2822-2024·2024-09-04

    BVI CustomEyes Procedure Pack Syringes Voluntarily Recalled Nationwide

    Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-M Inc. due to a voluntary manufacturer recall of certain syringe types distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000759;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2790-2024·2024-09-04

    BVI CustomEyes Procedure Packs Containing Sol-M Syringes Recalled Voluntarily

    BVI CustomEyes Procedure Packs containing low dead space and luer slip syringes from Sol-Millennium Medical are being voluntarily recalled.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584727;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2931-2024·2024-09-04

    BVI CustomEyes Procedure Packs containing Sol-M syringes recalled

    Beaver Visitec International recalls CustomEyes Procedure Packs because they contain Sol-Millennium Medical syringes subject to a voluntary recall. Fourteen units distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001973;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2885-2024·2024-09-04

    BVI CustomEyes Procedure Packs recalled due to Sol-M syringes

    BVI CustomEyes Procedure Packs containing Sol-M syringes are being recalled due to a voluntary manufacturer recall of the syringe components included in these procedure packs.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001568;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2902-2024·2024-09-04

    BVI CustomEyes Procedure Packs Containing Sol-M Syringes Recalled

    Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing low dead space and luer slip tip syringes manufactured by Sol-Millennium Medical. The voluntary recall affects 29 units distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001695;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2835-2024·2024-09-04

    FDA Recalls BVI CustomEyes Procedure Packs Containing Sol-M Syringes

    Beaver Visitec International has voluntarily recalled BVI CustomEyes Procedure Packs containing syringes manufactured by Sol-Millennium Medical. The affected procedure packs were distributed nationwide in the United States.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000985;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V097000·2024-09-02

    2021-2022 Ford E-350 and E-450 Power Steering Fluid Loss Recall

    Ford is recalling certain 2021-2022 E-350 and E-450 vehicles due to a defective power steering connection that may cause loss of power steering fluid and brake assist.

    Product
    FORD — 2021 FORD E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V100000·2024-09-02

    Mercedes-Benz recalls 2021-2023 vehicles for ground cable fire risk

    Mercedes-Benz USA is recalling 2021-2023 models including AMG GT53, CLS450, E450, and others because the 48-volt ground cable connection may not be tightened properly, risking fire.

    Product
    MERCEDES-BENZ — 2023 MERCEDES-BENZ AMG GT53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V094000·2024-09-02

    2024 Coachmen Catalina Travel Trailers Recalled for Tire Puncture Risk

    Forest River is recalling 2024 Coachmen Catalina and Forest River Aurora travel trailers because the tire may contact the slide adjustment bolt and puncture. A punctured tire can cause loss of vehicle control and increase crash risk.

    Product
    COACHMEN — 2024 COACHMEN CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V108000·2024-09-02

    2023 Infiniti QX60 Second-Row Seat May Fail to Lock Properly

    The second-row adjustable seat may extend past its stopper and fail to lock in certain 2023 Infiniti QX60 vehicles. This defect could prevent proper occupant restraint during a crash, increasing injury risk.

    Product
    INFINITI — 2023 INFINITI QX60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24350·2024-08-29

    HALO 1000 Portable Power Stations Recalled for Fire and Burn Hazards

    About 5,740 HALO 1000 Portable Power Stations are recalled because their lithium-ion batteries can overheat and catch fire. One death from smoke inhalation and four fire incidents have been reported.

    Product
    HALO 1000 Portable Power Stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24352·2024-08-29

    Glow in Dark Party Supplies Toy Sets Recalled for Battery Ingestion Hazard

    Glow in Dark Party Supplies Toy Sets sold on Amazon contain button cell batteries in Bunny Ears Headbands that can be easily accessed by children, posing a serious ingestion hazard. The sets violate federal battery-operated toy regulations.

    Product
    Glow in Dark Party Supplies Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24351·2024-08-29

    Fisher-Price Dumbbell Toy Recalled for Choking Hazard

    Fisher-Price is recalling a plastic dumbbell toy sold in the Baby Biceps Gift Set because the gray caps on the ends can come off, posing a choking hazard to infants. The firm has received seven reports of the ends coming off but no injuries have been reported.

    Product
    Dumbbell toy sold with Baby Biceps Gift Set
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2636-2024·2024-08-28

    McGrath Mac Video Laryngoscope battery depletion may cause thermal event and explosion

    McGrath Mac Video Laryngoscope devices may experience battery management system failures causing batteries to deplete below design thresholds, potentially resulting in thermal events and explosions.

    Product
    McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2587-2024·2024-08-28

    ClotTriever XL Catheter instructions updated to prevent device entrapment and embolism

    Inari Medical has updated instructions for the ClotTriever XL Catheter (30 mm) to prevent device entrapment and pulmonary embolism. Approximately 2,488 units distributed worldwide are affected.

    Product
    ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0638-2024·2024-08-28

    FDA Class I Recall: B. Braun Sodium Chloride Injection for Particulate Matter

    B. Braun Medical Inc. is recalling 63,444 containers of 0.9% Sodium Chloride Injection USP nationwide due to the presence of particulate matter. This intravenous medication may pose a serious health risk if administered to patients.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2637-2024·2024-08-28

    McGRATH MAC EMS Video Laryngoscope Battery Management System Recall

    Covidien is recalling McGRATH MAC EMS Video Laryngoscopes due to a battery management system defect that may deplete below design specifications, creating risk of thermal events and explosion. About 10,449 units were distributed worldwide.

    Product
    McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , Non-Sterile, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2641-2024·2024-08-28

    Bottle Decanter REF 2004S Recalled for Sterile Barrier Packaging Defects

    Microtek Medical Inc. is recalling Bottle Decanter REF 2004S units due to pin holes and tears found in the sterile barrier packaging during testing. Compromised packaging could allow contamination of the medical device.

    Product
    Bottle Decanter, REF 2004S. Packaged on a form, fill and seal machine with a poly/Tyvek material then placed 50 products to a case (cs).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2656-2024·2024-08-28

    Ophthalmic Surgical Knives Recalled Due to Sharpness Issues

    Alcon Research LLC is recalling certain ophthalmic knives (20 Gauge V-Lance model) due to complaints about sharpness. The affected units may not function properly during eye surgery.

    Product
    Product Desc: Product Name: 20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2660-2024·2024-08-28

    Ophthalmic surgical knives recalled for increased reports of dulled blades

    Alcon recalls specific ClearCut and A-OK ophthalmic surgical knives after reports of reduced blade sharpness. About 7,598 units were distributed nationwide and internationally.

    Product
    Product Desc: Product Name: CLEARCUT HP2 DB SLIT 3.2MM ANGCE Model/Catalog Number: 8065983265 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2674-2024·2024-08-28

    Alcon ophthalmic surgical knives recalled for sharpness defects

    Alcon Research LLC recalls ClearCut and A-OK ophthalmic surgical knives due to increased reports of sharpness issues that may affect surgical performance.

    Product
    Product Name: TOTALPLUS,25+ 7.5CPM VALV WD6 Model/Catalog Number: 8065751618 Software Version: N/A Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2680-2024·2024-08-28

    Alcon Ophthalmic Knives Recalled Due to Sharpness Defect Complaint Increase

    Alcon is recalling ClearCut and A-OK Corneal/Scleral ophthalmic knives due to increased complaints about sharpness. The recall affects 6,972 units distributed nationwide and internationally.

    Product
    Product Name: 25+TTLPL VPK 20000CPM BEV VAL Model/Catalog Number: 8065753106 Software Version: N/A Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide