The Recall Desk

State

Mississippi product recalls

20,199 recalls have nationwide distribution and so reach Mississippi. 0 additional recalls listed Mississippi specifically in their distribution scope.

About recalls in Mississippi

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 Mississippi 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.

8701–8725 of 20199

  • HighFDA (Devices)·Z-2145-2024·2024-06-26

    FDA Recalls VICRYL Plus Antibacterial Sutures Due to Packaging Defect

    Ethicon is recalling VICRYL Plus Antibacterial Sutures due to a packaging machine defect that created holes in the primary packaging, potentially compromising product sterility. Affected sutures may pose an infection risk.

    Product
    VICRYL Plus Antibacterial (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, except for ophthalmic, cardiovascular and neurological tissues. PRODUCT CODE: VCP196H VCP417H VCP602H VCP603H VCP662H VCPB259H VCPB94
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0556-2024·2024-06-26

    Drug Recall: Eptifibatide Injection Due to Failed Degradation Specifications

    Eugia US LLC is recalling 15,500 vials of Eptifibatide injection nationwide due to failed impurities and degradation specifications. The defect involves a related substance identified as Eptifibatide dimer.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·24281·2024-06-25

    MGA Entertainment Recalls Miniverse Make It Mini Sets with Liquid Resins

    MGA Entertainment recalls about 21 million Miniverse Make It Mini Sets with unused liquid resins due to risk of skin, eye, and respiratory irritation. The recalled sets contain acrylates in amounts prohibited in children's products.

    Product
    Miniverse Make It Mini Sets with Liquid Resins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24272·2024-06-20

    JoyJolt Declan Glass Coffee Mugs Recalled for Burn and Laceration Hazards

    MM Products is recalling about 580,000 JoyJolt Declan single-wall glass coffee mugs because they can break and crack when filled with hot liquids, posing burn and laceration hazards. The mugs were sold online from September 2019 through May 2022.

    Product
    JoyJolt Drinkware Declan Single-Wall Glass Coffee Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24273·2024-06-20

    Frontgate Newport Chaise Lounge Chairs Recalled for Finger Crushing and Amputation

    Cinmar recalls approximately 70,000 Frontgate Resort Collection Newport aluminum and teak chaise lounge chairs because the adjustable backrest can descend with force while seated, causing finger crushing and amputation injuries.

    Product
    Frontgate Resort Collection Newport Aluminum and Teak Chaises
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24271·2024-06-20

    myCharge POWER HUB Portable Chargers Recalled for Fire and Burn Hazards

    myCharge is recalling about 567,000 POWER HUB All-In-One 10,000mAh portable chargers sold exclusively at Costco from January 2022 through November 2023 because they can overheat while charging, posing fire and burn hazards. Two residential fires and property damage totaling approximately $165,000 have been reported.

    Product
    myCharge POWER HUB All-In-One 10,000mAh portable chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24270·2024-06-20

    Yeti Link Expansion Modules and EC8 Cables Recalled for Fire and Burn Hazards

    Goal Zero is recalling about 34,460 Yeti Link Expansion Modules and EC8 Cables because the connections can overheat and melt, posing fire and burn hazards. Two reports of cables melting inside vehicles have been received with minor property damage but no injuries.

    Product
    Yeti Link Expansion Modules and EC8 Cables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24278·2024-06-20

    Orly Lavender Scented Candles Recalled for Fire and Burn Hazards

    CBOCS Distribution Inc. is recalling about 3,600 lavender scented candles in wooden bread bowls sold at Cracker Barrel Old Country Store from November 2023 through May 2024. The candle flames can reach excessive heights and ignite the wooden bowl, posing fire and burn risks.

    Product
    Lavender scented candles in a round wooden bread bowl
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24274·2024-06-20

    Theefun Kids Gardening Tools Sets Recalled for Excess Phthalates

    Theefun Kids Gardening Tools Sets (model HJL-001) are recalled because the brown handle strings contain phthalates that exceed federal safety limits. Phthalates are toxic if ingested by young children.

    Product
    Theefun Kids Gardening Tools Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24269·2024-06-20

    StyleCraft Instinct Cordless Hair Clippers Recalled for Fire and Burn Hazards

    StyleCraft is recalling about 50,000 Instinct Professional Vector Motor Cordless Hair Clippers because the lithium-ion battery can overheat, posing fire and burn hazards. Six incidents of battery overheating or fire have been reported, including one minor burn.

    Product
    Instinct Professional Vector Motor Cordless Hair Clippers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24275·2024-06-20

    Babboe Cargo Bicycles Recalled for Frame Cracking and Fall Hazard

    Babboe cargo bicycles manufactured by Babboe B.V. are being recalled because their frames can crack, bend, and break, posing a fall hazard to riders. The recall affects about 300 units sold in the United States through bicycle retailers nationwide between January 2011 and March 2024.

    Product
    Cargo bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24277·2024-06-20

    Head Rush Technologies Recalls TRUBLUE iQ Auto Belay Devices for Fall Hazard

    Head Rush Technologies is recalling TRUBLUE iQ Auto Belay Devices because they can fail to retract, creating a risk of serious injury or death from falls. About 2,200 units were sold online from November 2022 through February 2024.

    Product
    TRUBLUE iQ Auto Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24279·2024-06-20

    Cedona Natural View Six-Drawer Dressers Recalled for Tip-Over Hazard

    Global Homes USA is recalling about 400 Cedona Natural View six-drawer dressers sold at Rooms To Go for tip-over and entrapment hazards that can injure or kill children if not anchored to a wall.

    Product
    Cedona Natural View six-drawer dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24276·2024-06-20

    Vitamix Blending Containers and Blade Bases Recalled for Laceration Hazard

    Vitamix Ascent and Venturist Series 8-ounce and 20-ounce blending containers and blade bases can separate from their bases, exposing sharp blades. The company has received 27 reports of lacerations, including 11 from a previous 2018 recall.

    Product
    Vitamix Ascent® Series and Venturist® Series 8-ounce and 20-ounce Blending Containers and Blade Bases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0554-2024·2024-06-19

    Docetaxel Injection Recalled Nationwide for Stopper Particulate Matter

    Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper contaminating the drug. The recall affects 2,806 vials distributed nationwide.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1345-2024·2024-06-19

    Baraka Brand Ground Black Pepper Recalled for Potential Salmonella Contamination

    U.B.C. Food Distributors is recalling Baraka brand ground black pepper due to potential Salmonella contamination. The product is packaged in 7oz retail containers with UPC 8 22514 26626 6.

    Product
    Baraka brand ground black pepper packaged in 7oz retail containers with UPC 8 22514 26626 6; 10 units per case
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1921-2024·2024-06-19

    Thoratec HeartMate System Monitor display malfunction in left ventricular assist devices

    The Thoratec HeartMate System Monitor is being recalled due to display malfunctions affecting 4,842 devices worldwide. These issues may prevent proper monitoring and device control.

    Product
    Thoratec HeartMate System Monitor, REF: 1286, L1286, 1286A, L1286A, 1286A-US, L1286A-US, 1286C, L1286C, L1386, 1286A-CAN, 1286INT and L1286INT. Left ventricular assist device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0553-2024·2024-06-19

    Docetaxel Injection Recalled Due to Particulate Matter in Stopper

    Sagent Pharmaceuticals is recalling Docetaxel Injection due to particulate matter from the vial stopper. Lot F1040001 was distributed nationwide.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL ANHYDROUS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1347-2024·2024-06-19

    Mt. Capra Goat Milk Formula Kit Recalled for Lack of FDA Premarket Notification

    Mt. Capra Goat Milk Formula Recipe Kit recalled for marketing as infant formula without FDA premarket notification.

    Product
    Mt. Capra Goat Milk Formula Recipe Kit (net wt. 10lbs. 8oz.) and Bundle Refill. Each Goat Milk Formula Recipe Kit consist of 10 individually packaged ingredients: *Whole Goat Milk *Goat Milk Lactose *Goat Milk Ghee -Extra Virgin Olive Oil -Expeller-Pressed Grapeseed Oil
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2024·2024-06-19

    Stimuplex A Anesthesia Needles Recalled for Undisclosed DEHP in Glue

    B Braun Medical Inc is recalling 108,811 units of Stimuplex A anesthesia needles because the devices are labeled as DEHP-free but the glue contains traces of DEHP.

    Product
    Stimuplex A, 30 DEG, 20GX6", 0.90x150mm, Catalogue Number: 4894278
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2141-2024·2024-06-19

    Fresenius AquaA hemodialysis water purification device pressure control malfunction

    Fresenius is recalling 4 hemodialysis water purification devices for pressure control malfunctions. When concentrate pressure exceeds the 19.9 bar limit, the device stops supplying water and halts dialysis treatment.

    Product
    US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of water to be used for hemodialysis Vivonic Part Numbers: G02020110 Fresenius Part Number: 24-090A-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0546-2024·2024-06-19

    Zilretta Injectable Drug Recalled for Failed Stability Specifications

    Pacira Pharmaceuticals is recalling 43,768 kits of Zilretta injectable suspension due to failed stability specifications at 2–8°C storage for 12 months followed by 25°C for 6 weeks. No illnesses or injuries have been reported.

    Product
    ZILRETTA — ZILRETTA (TRIAMCINOLONE ACETONIDE EXTENDED-RELEASE INJECTABLE SUSPENSION)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2040-2024·2024-06-19

    Cardiac SPECT System Recalled for Defective Service Handle Fastening

    GE Medical Systems is recalling MyoSPECT cardiac imaging systems due to service handles on internal lead covers that could loosen or release, potentially causing the cover to drop and injure service personnel. The recall affects 133 devices distributed worldwide.

    Product
    MyoSPECT System, Model H3912AA and H3912B, and MyoSPECT ES System, Model H3912AB and H3912BD, dedicated cardiac SPECT (single photon emission computerized tomography system).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2033-2024·2024-06-19

    Streptococcal A Rapid Test Kits Recalled for Unauthorized Distribution

    Wondfo USA is recalling 102,500 units of IMCO Strep A Rapid Test Kits due to unauthorized distribution for at-home, over-the-counter, and direct-to-consumer use.

    Product
    Independent Medical Co-op Inc., Streptococcal A rapid test kits, labeled as: IMCO Strep A Rapid Test Strip and IMCO Strep A Rapid Test, Part Number STP25-IMC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2139-2024·2024-06-19

    Aeos Robotic Digital Microscope recalled for safety mechanism failure

    Aesculap Inc is recalling Aeos Robotic Digital Microscope models with Product Code PV010 due to failure of the integrated safety mechanism. The robotic arm may drop more than 10 cm from its original position after the emergency stop button is pressed.

    Product
    Aeos Robotic Digital Microscope, Product Code: PV010
    Category
    Medical Device
    Distribution
    Distributed nationwide