The Recall Desk

State

Mississippi product recalls

73,381 recalls have nationwide distribution and so reach Mississippi. 5,377 additional recalls listed Mississippi specifically in their distribution scope.

What the numbers show

Total
5,377
Critical
933
Severe
1,346
Most recent
2026-09-23

Of the 5,377 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 1,346 (25%) are Severe.

These figures cover only the 5,377 recalls whose distribution notice names Mississippi specifically. The 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19501–19525 of 78758

  • HighCPSC·23042·2022-11-10

    Mockingbird Single-to-Double Strollers Recalled Due to Fall Hazard

    Mockingbird Single-to-Double Strollers may have cracks in the frame that pose a fall risk to children. The manufacturer has received 138 reports of frame cracks, including 8 injuries, and is offering free frame reinforcement kits.

    Product
    Mockingbird Single-to-Double Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V834000·2022-11-10

    2023 International MV vehicles recalled for loose wheel hub risk

    Navistar is recalling 2023 International MV vehicles because locking clips on the wheel hub retaining nut may be damaged, causing the wheel hub to loosen and separate from the axle housing, which increases crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V835000·2022-11-10

    RAM 2500 and 3500 transmission fluid leak increases fire risk

    RAM is recalling certain 2500 and 3500 vehicles due to transmission fluid leaks that could cause fires. Dealers will replace the affected components at no cost.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23041·2022-11-10

    Hunter Fan Recalls Five Lighting Collections Due to Electric Shock Hazard

    Hunter Fan Company is recalling approximately 2,600 light fixtures from five collections because internal wires can become damaged, posing an electric shock hazard. Consumers should stop using the products immediately and contact Hunter for a full refund.

    Product
    Hunter branded Devon Park, Astwood, Highland Hill, Kerrison and Van Nuys light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0153-2023·2022-11-09

    CritiCool Thermoregulation Device Recalled Due to Pump Failure

    The CritiCool thermoregulation device may experience premature pump failure leading to a HALT 4 error from which the device cannot recover, potentially delaying treatment. One death has been reported.

    Product
    CritiCool, thermoregulation device
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V832000·2022-11-09

    Motorhome interior step tread may detach, increasing fall injury risk

    Holiday Rambler and Fleetwood motorhomes (2022–2023) have interior step treads that may be improperly secured and can detach when stepped on, creating a fall hazard.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD INVICTA, VACATIONER, BOUNDER, FORTIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0158-2023·2022-11-09

    Surgical Cataract Pack Recalled Due to Compromised Sterile Packaging

    Medline Industries is recalling 300 units of Bausch + Lomb Cataract Packs due to breather pouches with seal openings that may compromise sterility. The affected surgical kits were distributed nationwide.

    Product
    BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0082-2023·2022-11-09

    Domino and C&H Sugar recalled for potential metal wire contamination

    Domino Foods Inc is recalling Domino and C&H Granulated Pure Cane Sugar (Easy Baking Tub) due to potential contamination with metal wire from a broken screen. The recalled product was distributed to distribution centers in 22 states.

    Product
    Domino and C&H Granulated Pure Cane Sugar Easy Baking Tub packaged in 3.5lb plastic tubs 6 tubs per case
    Category
    Food
    Distribution
    22 states
  • HighFDA (Food)·F-0120-2023·2022-11-09

    Cottage Cheese Products Recalled for Possible Plastic Foreign Objects

    Multiple cottage cheese brands are recalled due to possible plastic foreign objects. The recall affects 391,824 cases distributed to 38 states.

    Product
    Hannaford Cottage Cheese, 16oz and 24 oz; Hood Country Style Cottage Cheese, 16 oz, 24 oz., 32 oz.; Hood Large Curd Cottage Cheese, 16 oz; IGA Cottage Cheese, 16 oz; IGA Large Curd Cottage Cheese, 16 oz; Market Basket Cottage Cheese, 16 oz, 24 oz; Weis Cottage Cheese, 16 oz and…
    Category
    Food
    Distribution
    39 states
  • HighFDA (Food)·F-0123-2023·2022-11-09

    Hood Cottage Cheese with Blueberries Recalled for Plastic Contamination

    HP Hood LLC is recalling Hood Cottage Cheese with Blueberries (16 oz) because the product may contain plastic pieces. Affected products have best-by dates between October 24, 2022 and December 12, 2022.

    Product
    Hood Cottage Cheese with Blueberries, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Food)·F-0125-2023·2022-11-09

    Hood and Penn Maid Cottage Cheese Recalled for Possible Plastic Contamination

    HP Hood LLC is recalling Hood and Penn Maid cottage cheese with pineapple and cherry due to possible plastic foreign objects. Affected products have best-by dates between October 24, 2022 and December 12, 2022.

    Product
    Hood Cottage Cheese with Pineapple & Cherry, 16 oz; Penn Maid Cottage Cheese with Pineapple & Cherry, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Drugs)·D-0030-2023·2022-11-09

    Ceftazidime Intravitreal Solution Recalled for Sterility Assurance Failure

    Vital Care Compounder is recalling Ceftazidime intravitreal injection solutions due to manufacturing conditions that cannot guarantee product sterility. Affected lots were distributed to patients in Alabama, Louisiana, Mississippi, and Tennessee.

    Product
    CEFTAZIDIME INTRAVITREAL 2.25MG/0.1ML Solution, 0.5 mL syringe, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0044-2023·2022-11-09

    Compounded Injectable Drug Recalled Due to Sterility Assurance Defect

    A compounded injectable medication containing papaverine, phentolamine, and prostaglandin was recalled after FDA inspection found it was not produced under conditions that guarantee sterility. The product was distributed in Alabama, Louisiana, Mississippi, and Tennessee.

    Product
    PAPAVERINE / PHENTOLAMINE / PROSTAGLANDIN INJ 75MG/2.5MG/50MCG/ BOTTLE SOLUTION, 5 ML vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-0170-2023·2022-11-09

    Aneurysm Embolization System Detachment Controller Recalled for Manufacturing Defect

    MICROVENTION is recalling WEB Detachment Controllers due to an out-of-specification tunnel opening that may prevent proper implant detachment. This defect could delay treatment and cause vessel damage from implant manipulation.

    Product
    WEB Detachment Controller, REF: WDC-2, WDC, MV-WDC2. Component of WEB Aneurysm Embolization System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0042-2023·2022-11-09

    Pharmacy Plus Injectable Drug Recall Due to Sterility Assurance Failure

    Pharmacy Plus, Inc. recalled a compounded injectable medication (56 vials) due to manufacturing processes that cannot guarantee product sterility. Distributed in Alabama, Louisiana, Mississippi, and Tennessee.

    Product
    PAPAVERINE / PHENTOLAMINE / PROSTAGLANDIN 150MG / 2.5MG / 50MCG SOLUTION, 5 mL vials, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0051-2023·2022-11-09

    Prescription eye drops recalled due to sterility assurance defect

    Vital Care Compounder is recalling 378 droptainers of PRED ACETATE/GATIFLOXACIN eye drops distributed in AL, LA, MS, and TN due to inability to guarantee manufacturing sterility. No illnesses have been reported.

    Product
    PRED ACETATE / GATIFLOXACIN 1% / 0.5% SUSP, 10 mL droptainers, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-0157-2023·2022-11-09

    Bausch + Lomb Ophthalmic Surgical Kits Recalled for Sterile Packaging Defect

    Medline Industries is recalling 800 Bausch + Lomb Basic Ophthalmic surgical kits (Lot 22DBN365) for defective breather pouch seals. Opened seals in the packaging compromise the sterile conditions required for surgical procedures.

    Product
    BAUSCH + LOMB BASIC OPHTHALMIC PACK, REF LYN023BSBLB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0106-2023·2022-11-09

    Bella Cucina Walnut Sage Pesto recalled for undeclared milk allergen

    Bella Cucina Artful Food is recalling Walnut Sage Pesto because milk is present in the product but not declared on the label. Consumers allergic to milk should not consume this product.

    Product
    Bella Cucina Artful Food Walnut Sage Pesto Net Wt. 6 oz (169g) glass jar, UPC 6 19193 00041 6 Manufactured by Bella Cucina Artful Food Atlanta, GA 30310
    Category
    Food
    Distribution
    45 states
  • HighFDA (Food)·F-0124-2023·2022-11-09

    Hood Cottage Cheese Recalled for Possible Plastic Contamination

    HP Hood is recalling Hood Cottage Cheese with Cucumber & Dill (16 oz) because the product may contain plastic foreign objects. Consumers should not eat the recalled product.

    Product
    Hood Cottage Cheese with Cucumber & Dill, 16 oz
    Category
    Food
    Distribution
    39 states
  • HighFDA (Drugs)·D-0035-2023·2022-11-09

    Lidocaine/Phenylephrine Injectable Solution Recalled for Sterility Defect

    Pharmacy Plus Inc.'s Lidocaine/Phenylephrine injectable solution is recalled due to manufacturing process deficiencies that cannot guarantee product sterility. The recall affects 389 syringes distributed in Alabama, Louisiana, Mississippi, and Tennessee.

    Product
    LIDOCAINE/PHENYLEPHRINE PF SYR 1%/1.5% Solution, 3 mL syringes, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0034-2023·2022-11-09

    Laureth-9 Injectable Solution Recalled for Lack of Sterility Assurance

    A compounded Laureth-9 injectable solution has been recalled after the FDA found the manufacturing process could not guarantee sterility. The recalled product (lot 66513) was distributed in AL, LA, MS, and TN.

    Product
    LAURETH-9 INJ 2% Solution, 30 ML vial, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0057-2023·2022-11-09

    Voriconazole ophthalmic solution recalled for sterility concerns

    Pharmacy Plus, Inc. (Vital Care Compounder) is recalling Voriconazole Ophthalmic Solution 2% because FDA inspection found manufacturing processes cannot guarantee the product's sterility.

    Product
    VORICONAZOLE OPTH SOLUTION 2% STERILE SOLN, 10 ML droptainer, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-0040-2023·2022-11-09

    Moxifloxacin Preservative-Free Eye Drops Recalled for Sterility Assurance Failure

    Pharmacy Plus, Inc. is recalling Moxifloxacin 0.15 mg/0.1 mL preservative-free eye drops in 1 mL syringes due to lack of assured sterility. FDA inspection found the manufacturing process could not guarantee the product's sterility.

    Product
    MOXIFLOXACIN PRESERVATIVE FREE SYR, 0.15 mg/0.1 mL, Sterile Solution, 1 mL syringes, Rx only, Vital Care Compounder, 115 S. 40th Ave., Hattiesburg, MS 39402
    Category
    Drug
    Distribution
    4 states