The Recall Desk

State

Minnesota product recalls

20,082 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.

6201–6225 of 20082

  • HighNHTSA·25V001000·2025-02-01

    Aston Martin Vehicles Recalled: Infotainment Display Obstructs Rearview Camera

    Aston Martin is recalling certain 2024-2025 DB12, Vantage, and DBX707 vehicles. The infotainment home screen menu may obstruct the rearview camera when in reverse, reducing rear visibility and increasing the risk of a crash.

    Product
    ASTON MARTIN — 2024 ASTON MARTIN DB12
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V030000·2025-02-01

    Jaguar I-PACE vehicles recalled for insufficient pedestrian warning sounds

    Jaguar is recalling 2021-2022 I-PACE vehicles because they fail to produce sufficient pedestrian warning sounds when stationary or in reverse, violating federal safety standards. Dealers will update the audio amplifier software at no charge.

    Product
    JAGUAR — 2022 JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V031000·2025-02-01

    Land Rover Range Rover Sport PHEV Pedestrian Warning Sound Defect

    Land Rover is recalling certain 2020-2022 Range Rover PHEV and Range Rover Sport PHEV vehicles because they fail to make sufficient warning sounds when stationary and in reverse, violating federal safety standards for hybrid and electric vehicles.

    Product
    LAND ROVER — 2021 LAND ROVER RANGE ROVER SPORT PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25114·2025-01-30

    Portable Folding Stadium Seats Recalled Due to Fall and Injury Hazards

    AMX Global is recalling about 22,500 portable folding stadium seats because security hooks can crack and break, posing fall and injury risks. The company received reports of hook failures including falls and an injury.

    Product
    AMX Global Portable Folding Stadium Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25112·2025-01-30

    Hair Dryers Recalled for Missing Immersion Protection, Electrocution Risk

    AliExpress is recalling about 980 Multi Styler Hair Dryers sold online from May 2023 through November 2024 because they lack an immersion protection device and pose an electrocution hazard if they fall into water while plugged in.

    Product
    6-in-1 Multi Styler and 5-in-1 Multi Styler Hair Dryers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25109·2025-01-30

    Matrix-brand Training Cycles Recalled Due to Unexpected Seat Collapse

    Johnson Health Tech North America is recalling approximately 12,885 Matrix-brand Training Cycles due to seats that can unexpectedly lower during use. The company received 63 reports, including two falls, but no injuries have been reported.

    Product
    Matrix-brand Training Cycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25111·2025-01-30

    Digital Kitchen Scales Recalled for Coin Battery Ingestion Risk

    Greater Goods digital kitchen scales with easily accessible lithium coin batteries violate federal safety regulations due to missing child-resistant packaging and warnings. Ingestion of coin batteries can cause serious injury or death; no incidents have been reported.

    Product
    Greater Goods Digital Kitchen Scales
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25113·2025-01-30

    Girls pajamas recalled due to flammability regulation violation, burn-injury risk

    Cozchique, Tebbis, and Beeziac girls pajamas sold on Amazon violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. About 6,050 units distributed May through September 2024.

    Product
    Cozchique, Tebbis and Beeziac Girls Pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25110·2025-01-30

    Cabinet Health 4 oz. Refillable Medicine Bottles Recalled for Degrading Lids

    Cabinet Health is recalling about 65,000 refillable 4 oz. medicine bottles. The plastic lids can degrade with repeated use, losing child-resistance and posing a poisoning risk if children access the contents.

    Product
    Cabinet Health 4 oz. Refillable Medicine Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25115·2025-01-30

    Pearhead Infant Learning Toy Sets Recalled for Choking Hazard in Rattle

    Pearhead Infant Learning Toy Sets are recalled because the wooden egg-shaped rattle can lodge in a child's throat, creating a choking hazard. The recall affects about 2,700 units sold from August through October 2024.

    Product
    Pearhead Infant Learning Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0960-2025·2025-01-29

    VDR4 Phasitron Breathing Circuit Recalled for Potential Ventilation Reduction

    Percussionaire Corporation is recalling VDR4 Phasitron breathing circuit models due to a venturi component that may stick and reduce ventilation. This Class I recall affects over 4,700 units worldwide.

    Product
    VDR4 Phasitron Breathing Circuit Models that contain the venturi component: -A50094 D 5PK, Phasitron Kit, VDR, Single Patient, 5pk -A51001, VDR4 Control Unit Tester -PRT 991, VDR W/SWIVEL T SINGLE PATIENT PHASITRON -PRT 992, VDR4 HUMIDIFICATION ADAPTER KIT, CASE OF 10 -PRT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0207-2025·2025-01-29

    FOUZEE SugarLin Herbal Formula Capsules Recalled for Undeclared Prescription Drugs

    Shoppers-Plaza is recalling FOUZEE SugarLin Herbal Formula capsules because FDA testing found undeclared metformin and glyburide. The product was marketed without FDA approval.

    Product
    FOUZEE SugarLin HERBAL FORMULA capsules, 180 capsules per bottle, Sold and Distributed by Shoppers-Plaza, Hawthorne, CA 90250. Product of India. UPC 8 26656 69047 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1018-2025·2025-01-29

    Randox Lipoprotein (a) Diagnostic Assay Lacks FDA Clearance, Recalled

    Randox Laboratories is recalling 33 Randox Lipoprotein (a) diagnostic kits nationwide. The assay's claims for use on Roche Cobas c501 analyzers lack required FDA clearance or approval.

    Product
    Randox Lipoprotein (a) - In vitro diagnostic (IVD) use as Randox Lipoprotein (a) assay on automated analysers. Catalog Number: LP2757
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0989-2025·2025-01-29

    CardioMEMS Heart Failure Monitoring System Cloud Migration Causes Inaccurate Pressure Readings

    St. Jude Medical recalled 431 CardioMEMS HF pressure measurement systems after a cloud data migration reverted systems to outdated configuration, causing inaccurate pulmonary artery pressure readings.

    Product
    CARDIOMEMS HF PRESSURE MEASUREMENT SYSTEM CardioMEMSTM HF System Hosptial Electronics System (PES) REF CM3000 Merlin.net Patient Care Network (PCN) Heart Failure Web Application (Which interfaces with CardioMEMSTM HF System Patient Electronics System (PES) and CardioMEMSTM HF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1012-2025·2025-01-29

    Dressing change kits recalled due to packaging defect compromising sterility

    Trinity Sterile is recalling Dressing Change Kits with ChloraPrep and HaloGUARD due to potential holes in the package that could compromise product sterility. The recall affects 1,980 units distributed across multiple states.

    Product
    Brand Name: IMed Products Product Name: Dressing Change Kit with ChloraPrep 3mL & HaloGUARD Model/Catalog Number: IM46062 Software Version: N/A Product Description: Dressing change kit, case of 30, lot #600022, 66 cases affected. Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1008-2025·2025-01-29

    Repeater Bone Tamp Recalled for Component Incompatibility in Spinal Fusion

    Integrity Implants Inc. is recalling Repeater Bone Tamp devices (Model ASY-00132) due to incompatibility between Revision A bone tamps and Revision C bone funnels used in spinal fusion procedures.

    Product
    Brand Name: N/A Product Name: Repeater Bone Tamp Model/Catalog Number: ASY-00132 Software Version: N/A Product Description: The Repeater Bone Tamp is a cylindrical shaft used to push bone graft material through a corresponding bone funnel into the FlareHawk interbody fusion d
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1003-2025·2025-01-29

    Olympus Thunderbeat Surgical Instruments Recalled for Probe Tip Damage

    Olympus is recalling Thunderbeat hand instruments (Model TB-0535FCS) because probe tips can be damaged or break during use. The recall affects 27,352 units distributed internationally.

    Product
    Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: Thunderbeat, 5MM, 35CM, Front-actuated Grip Type S¿ Model Number: TB-0535FCS Catalog Number/Product Code: N5423810 Software Version: N/A Product Description: Thunderbeat instrument is a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1016-2025·2025-01-29

    Dressing Change Tray Recalled Due to Potential Package Sterility Compromise

    Trinity Sterile's Dressing Change Tray (Model TM6180CP, Lot 600032) is recalled because of a potential hole in the package that could compromise sterility. The recall affects 280 units distributed across Maryland, Pennsylvania, Tennessee, and Texas.

    Product
    Brand Name: Tacy Medical, Inc. Product Name: Dressing Change Tray CS/20 Model/Catalog Number: TM6180CP Software Version: N/A Product Description: Dressing change tray, case of 20, lot #600032, 50 cases affected. Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0982-2025·2025-01-29

    Stryker 3.0MM Neuro Precision Head Recalled for Package Labeling Mismatch

    Stryker is recalling the 3.0MM Precision Neuro Match Head due to a packaging discrepancy where the device may not match the product label. Approximately 1,489 units distributed worldwide are affected, including lot numbers 22179047, 22179027, and 22160017.

    Product
    stryker 3.0MM Precision Neuro Match Head, REF 5820-107-530, used to cut bone and bone cement during neurosurgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1005-2025·2025-01-29

    Medical Analyzer Software May Fail to Alert of Expired Reagent Packs

    The VITROS 5600 Integrated System's software (version 3.8.0 and higher) may fail to notify users when Signal Reagent Packs expire. This could result in use of expired reagents, causing no results or erroneous results from tests.

    Product
    Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog Number: 6802413 (New), 6802415 (Certified/Refurbished), 6904001 (China) Software Version: version 3.8.0 or higher Product Description: In vitro diagnostic chemistry analyzer. FDA 3 letter product
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0985-2025·2025-01-29

    Medtronic Recalls EOPA Arterial Cannula Models for Labeling Errors

    Medtronic Perfusion Systems is recalling EOPA Arterial Cannula models 77418 and 77422 due to incorrect labeling on seven manufacturing lots. Approximately 930 units were distributed worldwide.

    Product
    EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1006-2025·2025-01-29

    Diagnostic analyzer software may fail to alert users to expired reagents

    VITROS XT 7600 Integrated System software may not warn users when Signal Reagent Packs expire, risking inaccurate or missing test results.

    Product
    Brand Name: VITROS Product Name: VITROS XT 7600 Integrated System Model/Catalog Number: 6844461 (New), 6272222 (Certified), 6904003 (China) Software Version: version 3.8.0 or higher Product Description: In vitro diagnostic chemistry analyzer. FDA 3 letter product code: JJE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1007-2025·2025-01-29

    VITROS 3600 Diagnostic System May Fail to Alert Users to Expired Reagents

    The VITROS 3600 Immunodiagnostic System may not properly alert users when Signal Reagent Packs expire, risking use of expired products and potentially inaccurate test results. Affected systems worldwide should be checked for this software issue.

    Product
    Brand Name: VITROS Product Name: VITROS 3600 Immunodiagnostic System Model/Catalog Number: 6802783 (New), 6802914 (Certified/Refurbished), 6904000 (China) Software Version: version 3.8.0 or higher Product Description: In vitro diagnostic chemistry analyzer. FDA 3 letter pr
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1004-2025·2025-01-29

    BD PCR Cartridges for MAX System signal drift in select lots

    Specific lots of BD PCR Cartridges used with the MAX System may experience signal drift, potentially affecting diagnostic accuracy. BD has initiated a recall of 516,435 affected units worldwide.

    Product
    BD PCR Cartridges used with MAX System. Model Number: 437519
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0998-2025·2025-01-29

    Olympus Thunderbeat Surgical Instrument Recalled for Damaged or Breaking Probe Tips

    Olympus is recalling approximately 9,200 units of Thunderbeat surgical hand instruments distributed worldwide because probe tips can become damaged, break, or pads can detach during use.

    Product
    Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45 cm,Front-actuated Grip Type S Model Number: TB-0545FCS Catalog Number/Product Code: N5423330 Software Version: N/A Product Description: Thunderbeat instrument is a s
    Category
    Medical Device
    Distribution
    Distributed nationwide