The Recall Desk

State

South Dakota product recalls

73,576 recalls have nationwide distribution and so reach South Dakota. 2,686 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total
2,686
Critical
401
Severe
747
Most recent
2026-10-14

Of the 2,686 recalls naming South Dakota we have scored against our rubric, 401 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 747 (28%) are Severe.

These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

676–700 of 76262

  • ModerateNHTSA·26T014000·2026-09-10

    Wheel Pros Recalls 549 Avix TrailTek RT Tires for Incorrect Markings

    Wheel Pros is recalling 549 Avix TrailTek RT tires because the sidewall is incorrectly labeled 'Not for Highway Use,' failing to meet federal safety standards.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0851-2026·2026-09-09

    Optimal Balance Pharmacy Recalls Contaminated Glutathione Injection Vials

    Optimal Balance Pharmacy is recalling 53 vials of Glutathione 200 mg/mL due to bacterial endotoxin contamination.

    Product
    Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3086-2026·2026-09-09

    Fresenius 5008X HD/HDF Blood Tubing Set Recalled for Leak Risk

    Fresenius Medical Care is recalling 18,600 units of 5008X HD/HDF blood tubing sets due to a heightened probability of blood leaks that could cause blood loss and hypovolemia.

    Product
    5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0819-2026·2026-09-09

    Baxter Recalls Vasopressin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Vasopressin in 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    VASOPRESSIN IN 0.9% SODIUM CHLORIDE — VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN IN 0.9% SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1309-2026·2026-09-09

    Hampton Grocer Lactation Granola Recalled for Salmonella Contamination Risk

    The Hampton Grocer is recalling Small Batch Lactation Granola due to potential Salmonella contamination. Consumers should stop eating the product and return it for a refund.

    Product
    THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS + MORINGA; SUPPORTS + PROMOTES HEALTHY LACTATION; INGREDIENTS Organic Gluten Free Oats Organic Maple Syrup Organic Pumpkin Seeds Organic Coconut Oil Almond Butter…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3085-2026·2026-09-09

    Fresenius 5008X Blood Tubing Set Recalled for Potential Blood Leak

    Fresenius Medical Care is recalling 5008X HD/HDF Standard Blood Tubing Sets due to a heightened probability of blood leak from the Arterial Alpha Clip connection.

    Product
    5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3061-2026·2026-09-09

    Medline Eye and Cataract Kits Recalled for Potential Sterility Breach

    Medline is recalling 2,080 eye and cataract preop kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A; 3) CATARACT PREOP KIT, Model Number: DYKS1583A; 4) CATARACT PREOP KIT, Model Number: DYKS1583B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3063-2026·2026-09-09

    Medline Blood Draw and Phlebotomy Kits Recalled for Sterility Breach

    Medline is recalling approximately 996,692 blood draw and phlebotomy kits due to potential sterility breaches in the packaging. The defect may expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D; 3) QP KIT, Catalog Number: DYNDB3005F; 4) DOUBLE RED CELL PHLEBOTOMY KIT, Catalog Number: DYNDB3006C; 5) PLATELET PHLEBOTOMY KIT, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V576000·2026-09-09

    Ford Recalls 2026 F-150s Due to Rear Axle Bearing Defect

    Ford is recalling 2026 F-150 vehicles because incorrect rear axle tail bearings may cause wheel lock-up or driveshaft separation, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0809-2026·2026-09-09

    Baxter Recalls Famotidine Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Famotidine Injection due to CGMP deviations. The product was distributed in the US, Puerto Rico, and Chile.

    Product
    FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0810-2026·2026-09-09

    Baxter Recalls Dexmedetomidine Hydrochloride Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Dexmedetomidine Hydrochloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0821-2026·2026-09-09

    Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Daptomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall covers the US, Puerto Rico, and Chile.

    Product
    Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0718-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3084-2026·2026-09-09

    Fresenius Medical Care Recalls 5008X Standard HD Pre-Flush Blood Tubing Sets

    Fresenius Medical Care is recalling 120 units of 5008X Standard HD Pre-Flush Blood Tubing Sets due to a heightened probability of blood leaks during treatment.

    Product
    5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3062-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 18,290 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number: DYKM1881A; 3) TRIMA KIT, Model Number: DYNDB3077C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E063000·2026-09-09

    Ford Recalls Battery Energy Control Modules for Software Defect

    Ford is recalling specific Battery Energy Control Modules (BECM) because software errors may cause incorrect charge readings or overheating, increasing crash and fire risks.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3048-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 104 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT, Model Number: ACC010741; 2) KIT ANESTHESIA L&D A- LINE SET, Model Number: DYKMBNDL199A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3057-2026·2026-09-09

    Medline Blood Culture Kits Recalled for Potential Sterility Breach

    Medline is recalling 3,650 blood culture kits nationwide due to potential packaging defects that may compromise sterility and expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number: DYNDH1487A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0817-2026·2026-09-09

    Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to CGMP deviations. The affected product was distributed in the US, Puerto Rico, and Chile.

    Product
    CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V583000·2026-09-09

    Daimler Trucks Recalls Freightliner and Western Star Trucks for Brake Defect

    Daimler Trucks North America is recalling certain 2020-2023 Freightliner Cascadia and 2022 Western Star 49X trucks because corroded brake valves may cause the vehicle to pull during braking.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0820-2026·2026-09-09

    Baxter Recalls Vancomycin Injection Due to CGMP Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Vancomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3060-2026·2026-09-09

    Medline C-Section Prep Kits Recalled for Potential Sterility Breach

    Medline is recalling 352 C-Section Prep kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) C-SECTION PREP, Model Number: DYNJ32702B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0814-2026·2026-09-09

    Baxter Recalls Nexterone Amiodarone Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Nexterone (amiodarone hydrochloride) injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    NEXTERONE — NEXTERONE (AMIODARONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V578000·2026-09-09

    Ford Recalls 2023-2027 F-150 Trucks for Fuel Tank Securing Defect

    Ford is recalling 2023-2027 F-150 vehicles because the fuel tank may be improperly secured, posing risks of fuel leaks, engine stalls, or the tank detaching while driving.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3053-2026·2026-09-09

    Medline Ultrasound Breast Pack Recalled for Potential Sterility Breach

    Medline is recalling 300 Ultrasound Breast Packs due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) ULTRASOUND BREAST PACK, Model Number: DYNJ63375C
    Category
    Medical Device
    Distribution
    Distributed nationwide