The Recall Desk

State

Mississippi product recalls

72,919 recalls have nationwide distribution and so reach Mississippi. 5,349 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total
5,349
Critical
923
Severe
1,126
Most recent
2026-09-09

Of the 5,349 recalls naming Mississippi we have scored against our rubric, 923 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,126 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,349 recalls whose distribution notice names Mississippi specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2601–2625 of 78268

  • HighFDA (Devices)·Z-1698-2026·2026-04-08

    da Vinci mega needle driver recalled over broken or frayed cables

    Intuitive Surgical is recalling da Vinci S and Si Mega Needle Driver Instruments following increased complaints of broken or frayed grip cables in reusable instruments.

    Product
    Brand Name: da Vinci S, Si Mega Needle Driver Instrument Product Name: da Vinci S, Si Mega Needle Driver Instrument Model/Catalog Number: 420194 Software Version: NA Product Description: EndoWrist Instruments or Da Vinci S/Si Reusable instruments, including blunt and sharp en
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1659-2026·2026-04-08

    Philips Allura Xper FD10C X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10C because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD10C; System Code: 722001;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1676-2026·2026-04-08

    Philips Azurion 7 B20 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 B20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1667-2026·2026-04-08

    Philips Allura Xper FD10 OR Table X-ray may not start reliably

    Philips is recalling the Allura Xper FD10 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10 OR Table; System Code: (1) 722022, (2)722033;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1677-2026·2026-04-08

    Philips Azurion 7 M12 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2026·2026-04-08

    Philips Azurion 3 M12 X-ray may not start from foot switch

    Philips is recalling the Azurion 3 M12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 3 M12; System Code: (1)722063, (2)722221, (3)722229;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1675-2026·2026-04-08

    Philips Azurion 7 B12 X-ray may not start from foot switch

    Philips is recalling the Azurion 7 B12 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1666-2026·2026-04-08

    Philips Allura Xper FD20 Biplane OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20 Biplane OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20 Biplane OR Table; System Code: (1) 722020, (2)722025;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1668-2026·2026-04-08

    Philips Allura Xper FD20/10 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/10 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/10; System Code: 722029;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1669-2026·2026-04-08

    Philips Allura Xper FD20/20 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20/20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/20; System Code: 722038;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1660-2026·2026-04-08

    Philips Allura Xper FD10F X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD10F because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD10F; System Code: 722002;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1670-2026·2026-04-08

    Philips Allura Xper FD20/20 OR Table X-ray may not start

    Philips is recalling the Allura Xper FD20/20 OR Table because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    Allura Xper FD20/20 OR Table; System Code: 722039;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1663-2026·2026-04-08

    Philips Allura Xper FD20 X-ray may not start from foot switch

    Philips is recalling the Allura Xper FD20 because X-ray imaging may not be initiated, or may occur intermittently, when using the wired foot switch.

    Product
    ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1687-2026·2026-04-08

    Artoura ultra high profile expander infusion needles may be blunt

    Mentor is recalling Artoura Breast Tissue Expanders in the smooth ultra high profile range because the infusion sets may contain a dull or blunt needle tip.

    Product
    Artoura Breast Tissue Expanders Reference Numbers: SDC-100UH SDC-110UH SDC-120UH SDC-130UH SDC-135UH SDC-140UH Smooth Ultra High Profile Tissue Expander, 350cc, 455cc, 535cc, 650cc, 700cc, 850cc
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1709-2026·2026-04-08

    Medline laryngoscopy bronchoscopy kits contain Olympus valves shedding rubber fragments

    Medline is recalling four bronchoscopy and laryngoscopy kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.

    Product
    Medline kits containing Olympus biopsy valves: 1. BRONCHOSCOPY, DYNJ900898I DYNJ901922G 2. FLEXIBLE BRONCHOSCOPY KIT, DYKM1417I DYKM1417J 3. LARYNGOSCOPY/BRONCHOSCOPY PACK, DYNJ58146A 4. RIGID KIT, DYNDA2138A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V221000·2026-04-08

    Forest River Recalls 2026 Travel Trailers Due to Incorrect Weight Labeling

    Forest River is recalling 2026 Westbrook and Avenger travel trailers because the Federal Placard label may list an incorrect dry weight, potentially leading to vehicle overloading.

    Product
    FOREST RIVER — FOREST RIVER AVENGER, WESTBROOK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V219000·2026-04-06

    Greenpower Recalls School Buses Due to Missing Mirror Warning Label

    Greenpower is recalling 2020-2024 Nano Beast and 2021-2024 Beast school buses because a warning label on the cross-view mirror may be missing, potentially increasing crash risk.

    Product
    GREENPOWER — GREENPOWER NANO BEAST SCHOOL BUS, BEAST SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V218000·2026-04-06

    2024 Genesis G90 seat belt anchors may detach in crash

    Hyundai is recalling certain 2023–2026 Genesis G90 vehicles because driver and passenger seat belt anchors may detach. Detached anchors cannot adequately restrain occupants in a crash, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI, GENESIS SANTA FE HYBRID, IONIQ 6, SANTA FE, G90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V217000·2026-04-06

    Pierce Recalls Firetrucks Due to Faulty Stabilizer Indicator Light

    Pierce Manufacturing is recalling 2015-2026 aerial firetrucks because a faulty light may falsely indicate the vehicle is stable, increasing injury risk during operation.

    Product
    PIERCE — PIERCE IMPEL, ENFORCER, ARROW XT, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·PHA-04012026-01·2026-04-06

    USDA Retracts Lead Alert for Dorada Chicken Nuggets

    USDA FSIS retracted a public health alert for Dorada chicken nuggets after follow-up testing confirmed the initial lead result was a laboratory error.

    Product
    Dorada Foods — FSIS Retracts Public Health Alert for Frozen, Ready-to-Eat Chicken Nuggets Due to Updated Laboratory Result
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V216000·2026-04-03

    Mercedes-Benz Recalls Vehicles for Drive Shaft Universal Joint Breakage Risk

    Mercedes-Benz is recalling specific 2018-2020 E-Class and S-Class models because the drive shaft universal joint may break, causing a sudden loss of drive power and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 560 4MATIC COUPE, E 450 4MATIC, E 400 4MATIC, E 400 4MATIC CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26379·2026-04-02

    HTRC and Haisito battery chargers can ignite causing fires

    Huizhou Haitan Technology is recalling T400 battery chargers because they can ignite or cause a connected battery to ignite. Thirty-three fires and explosions have been reported.

    Product
    HTRC and Haisito battery chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26377·2026-04-02

    Granitestone sauté pan handle screw caps can eject when heated

    E Mishan & Sons is recalling Granitestone Diamond Pro Blue sauté pans because the metal cap on the handle screw can detach and forcefully eject when heated. One injury has been reported.

    Product
    Granitestone Diamond Pro Blue Sauté Pans
    Category
    Consumer Product
    Distribution
    Distributed nationwide