The Recall Desk

State

Mississippi product recalls

73,584 recalls have nationwide distribution and so reach Mississippi. 5,379 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total
5,379
Critical
933
Severe
1,347
Most recent
2026-10-24

Of the 5,379 recalls naming Mississippi we have scored against our rubric, 933 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,347 (25%) are Severe.

These figures cover only the 5,379 recalls whose distribution notice names Mississippi specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

726–750 of 78963

  • 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
  • SevereFDA (Drugs)·D-0808-2026·2026-09-09

    Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations

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

    Product
    CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0834-2026·2026-09-09

    Teva Recalls Trazodone Hydrochloride Tablets Due to Foreign Material

    Teva Pharmaceuticals is recalling 175,392 bottles of Trazodone Hydrochloride 50 mg tablets because they may contain foreign tablets or capsules.

    Product
    TRAZODONE HYDROCHLORIDE — TRAZODONE HYDROCHLORIDE (TRAZODONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V582000·2026-09-09

    Ford Recalls 2023-2025 Mustang Mach E for Battery Software Defect

    Ford is recalling 2023-2025 Mustang Mach E vehicles with specific battery modules due to software errors that may cause power loss or fire.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3087-2026·2026-09-09

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

    Fresenius Medical Care is recalling 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 Twister Blood Tubing Set Part Number 03-5350-8
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0807-2026·2026-09-09

    Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling Daptomycin in Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Daptomycin, in 0.9% Sodium Chloride Injection, 500 mg per 50 mL (10 mg/mL), 500 mg total, in 50 mL Single Dose Container (24 bags/carton), Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0714-24.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3046-2026·2026-09-09

    AVID Medical Recalls Halyard Neurological Sponges Due to Endotoxin Variability

    AVID Medical is recalling specific lots of Halyard medical convenience kits containing Ritmed Neurological Sponges due to potential endotoxin level variability.

    Product
    Halyard medical convenience kits labeled as: 1) A-P PACK - 205936, Model/Item Number (kit) ANAP22-01; 2) POSTERIOR PACK - 205960, Model/Item Number (kit) ANPP15-01; 3) ANEURYSM PACK, Model/Item Number (kit) BPAY14-01; 4) SPINE PACK, Model/Item Number (kit) HSLM53-01…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V580000·2026-09-09

    Ford Recalls 2026 Bronco Vehicles Due to Air Bag Mounting Defect

    Ford is recalling 2026 Bronco vehicles because a metal burr on the side curtain air bag bracket may tear the bag during deployment, increasing injury risk.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0805-2026·2026-09-09

    Baxter Recalls Vancomycin Injection Due to Manufacturing 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
  • HighFDA (Devices)·Z-3059-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 3,752 Labor CDS and Vag Delivery Admission Bags due to packaging wrinkles that may compromise sterility, risking microbial contamination.

    Product
    Medline Convenience Kits: 1) LABOR CDS, Model Number: CDS981762B; 2) VAG DELIVERY ADMISSION BAG, Model Number: DYKA1054F
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3066-2026·2026-09-09

    Baxter Novum IQ Syringe Pump Recalled for Software Infusion Issue

    Baxter Healthcare is recalling four Novum IQ Syringe Pump loaner units due to a software issue that may occur during multi-syringe infusions.

    Product
    Baxter Novum IQ Syringe Pump, Loaner, Model Number 40800BAXUSL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3072-2026·2026-09-09

    Medline Blood Culture Kits Recalled Due to Potential Seal Defects

    Medline is recalling blood culture kits containing BD ChloraPrep applicators due to potential packaging seal defects that could lead to infection.

    Product
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BLOOD CULTURE KIT 2 W/CONNECT DYNDH1487A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3069-2026·2026-09-09

    Medline Convenience Kits Recalled Due to Potential Applicator Seal Defects

    Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators due to potential packaging seal defects that could lead to infection.

    Product
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators BASIN PACK-LF DYNJ42828B EYE BASIN TRAY-LF DYNJ42832B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3073-2026·2026-09-09

    Medline Blood Culture Kits Recalled Due to Incomplete Applicator Seals

    Medline is recalling blood culture kits containing BD ChloraPrep applicators with open or incomplete seals. The defect may allow contamination, posing a risk of infection.

    Product
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators ADULT BLOOD CULTURE KIT DYNDH1444D BLOOD CULTR KT DIVRSN DEVICE DYNDH1866 BLOOD CULTURE KIT DYNDH1462B DYNDH1622C DYNDH1622D DYNDH1622F DYNDH1715B DYNDH2028 DYNDH2048 BLOOD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3075-2026·2026-09-09

    Medline Convenience Kits Recalled Due to Potential Applicator Seal Defects

    Medline is recalling specific lots of convenience kits containing BD ChloraPrep applicators due to potential packaging seal defects that could allow contamination.

    Product
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators PATIENT ADMIN KIT DYKA1384B DYKA1384C WELCOME KIT DYKS1206D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3068-2026·2026-09-09

    Medline Convenience Kits Recalled Due to Potential Applicator Seal Defects

    Medline is recalling specific lots of Convenience Kits containing BD ChloraPrep Clear applicators because packaging seals may be open or incomplete, posing a risk of infection.

    Product
    Medline Convenience Kits containing BD ChloraPrep Clear - 1mL Applicators OPEN HEART CDS983348AA CDS983348AB
    Category
    Medical Device
    Distribution
    Distributed nationwide