The Recall Desk

State

Tennessee product recalls

72,940 recalls have nationwide distribution and so reach Tennessee. 7,819 additional recalls listed Tennessee specifically in their distribution scope.

What the numbers show

Total
7,819
Critical
1,317
Severe
1,653
Most recent
2026-09-09

Of the 7,819 recalls naming Tennessee we have scored against our rubric, 1,317 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,653 (21%) are Severe.

These figures cover only the 7,819 recalls whose distribution notice names Tennessee specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3101–3125 of 80759

  • HighFDA (Devices)·Z-1445-2026·2026-03-04

    Olympus 28 French resection sheath recalled over ceramic tip breakage

    Olympus is recalling its Resection Sheath, 28 Fr, model A22043A, used in urologic applications, after complaints that the ceramic tip of the resection sheath can break.

    Product
    Olympus Resection Sheath, 28 Fr.; Model No. A22043A. Resection sheath for urologic applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1432-2026·2026-03-04

    Medline nail kits recalled over saline wound wash sterility failure

    Medline is recalling Nail Kit convenience kits, model POD14214, because the manufacturer of the sterile saline wound wash they contain may not have met the required sterility assurance level.

    Product
    Medline Convenience Kits: 1) NAIL KIT, Model Number: POD14214
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1463-2026·2026-03-04

    Medline Kits with Tego Connectors Recalled Due to Silicone Seal Defects

    Medline Industries, LP is recalling specific Medline Kits containing Tego Connectors because the silicone seals may dome or tear, potentially causing fluid leakage or blocked paths.

    Product
    Medline Kits containing Tego Connectors: Medline IR Pack, SKU DYNJ67205C Medline NO CATHETER DIALYSIS INSERTION, SKU CVI5200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0527-2026·2026-03-04

    Yoyo Gummy Assorted Flavor Recalled Due to Unallowed Color Additive

    SB FOOD LLC is recalling Yoyo Gummy Assorted Flavor because the product contains Carmoisine (E122) - Acid Red 14, which is an unallowed color.

    Product
    Yoyo Gummy Assorted Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-1472-2026·2026-03-04

    Adapt Pump Medical Device Recalled Due to Microclimate Management Function Failure

    Agiliti Health - Ellis is recalling Adapt Pumps (Model 61600200) because the Microclimate Management function may fail to re-engage after using the Autofirm function.

    Product
    Adapt Pump, Model/Catalog Number: 61600200-Adapt Pump, component of Adapt support surfaces (Adapt Air, Adapt Air EX, Adapt Air Pro, Adapt Air Pro EX, Adapt Convertible, Adapt Convertible EX), sofware version 1.3.0; Mattress, Air Flotation, Alternating Pressure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0528-2026·2026-03-04

    FDA Recalls Yoyo Gummy Tropical Flavor Candy for Unauthorized Color Additive

    SB FOOD LLC is recalling Yoyo Gummy Tropical Flavor candy because it contains Carmoisine (E122), a color additive not approved for use in this product. The recalled product was distributed to 15 states.

    Product
    Yoyo Gummy Tropical Flavor, 2.8 Oz (80g) , Plastic Bag, 24 bags per case
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-1462-2026·2026-03-04

    Edermy PIE PAK units recalled for lacking FDA 510(k) clearance

    Edermy LLC is recalling PIE PAK models P2HC-A, P2HC-S and P2HC because the devices lack 510(k) clearance from the FDA.

    Product
    PIE PAK Models: P2HC-A, P2HC-S, P2HC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0343-2026·2026-03-04

    Eptifibatide Injection Labeling Error Recall by Slate Run

    Slate Run Pharmaceuticals is recalling Eptifibatide Injection due to a labeling error on the carton, which incorrectly describes the dosing instructions.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2026-EXP·2026-03-03

    Ajinomoto Recalls Chicken and Pork Fried Rice Due to Glass Contamination

    Ajinomoto Foods North America is expanding a recall for frozen fried rice, ramen, and shu mai products due to possible glass contamination. No injuries have been reported.

    Product
    Ajinomoto Foods North America — Ajinomoto Foods North America, Inc. Expands Recall for Chicken and Pork Fried Rice, Ramen, and Shu Mai Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·26V120000·2026-03-03

    Ford Recalls 2026 Lincoln Navigator for Driver Seat Software Defect

    Ford is recalling 2026 Lincoln Navigator vehicles because the driver seat software may malfunction at low speeds, causing the seat to move unexpectedly and increasing crash risk.

    Product
    LINCOLN — LINCOLN NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V124000·2026-03-03

    Ford Bronco and Edge Vehicles Recalled for Camera Software Issue

    Ford is recalling certain 2021-2026 Bronco and 2021-2024 Edge vehicles because the rearview camera may fail to display an image due to an overheating module.

    Product
    FORD — FORD BRONCO, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V123000·2026-03-03

    Lincoln Corsair and Ford vehicles recalled for rearview camera display issues

    Ford Motor Company is recalling certain 2020-2024 Lincoln and Ford vehicles because the center display may show an inverted rearview image, increasing crash risks.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER, ESCAPE, CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V117000·2026-03-03

    Ford and Lincoln vehicles recalled due to windshield wiper motor failure risk

    Ford Motor Company is recalling certain 2020-2022 Ford and Lincoln vehicles because the windshield wiper motors may fail, potentially reducing visibility and increasing crash risks.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, AVIATOR, EXPLORER, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V122000·2026-03-03

    2025 Ford Vehicles Recalled for EGR Valve Failure Risk

    Ford is recalling certain 2025 vehicles due to a potential EGR valve failure that could cause an unexpected loss of drive power, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, RANGER, MUSTANG, MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03012026-01·2026-03-01

    USDA Issues Public Health Alert for Punahele Beef Jerky Due to Undeclared Soy

    USDA FSIS issued a public health alert for Punahele beef jerky products containing undeclared soy lecithin. Consumers are advised not to consume the items.

    Product
    Punahele Jerky Company, Inc. — FSIS Issues Public Health Alert for Ready-To-Eat Beef Jerky Products Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalCPSC·26284·2026-02-26

    Royal Oak Flame Saber Lighters Recalled Due to Fire and Burn Hazards

    Royal Oak Enterprises is recalling approximately 190,560 Flame Saber Lighters because they lack required child-resistant mechanisms, posing a risk of serious injury or death.

    Product
    Royal Oak Flame Saber Lighters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26291·2026-02-26

    Grtard Magnetic Stick Figure Toy Sets Recalled Due to Ingestion Hazard

    Grtard is recalling approximately 130 Grtard Magnet Stick Figure Men Toy Sets because they contain loose magnets that pose a serious injury or death risk if swallowed.

    Product
    Grtard Magnet Stick Figure Men Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26288·2026-02-26

    Trankerloop Baby Bath Seats Recalled Due to Drowning Risk

    Trankerloop is recalling approximately 2,380 baby bath seats because they are unstable and can tip over, posing a risk of serious injury or death from drowning.

    Product
    Trankerloop Baby Bath Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26297·2026-02-26

    TheKiddoSpace Recalls Children's Montessori Egg Puzzle Toys Over Choking Hazard

    TheKiddoSpace is recalling its Children's Montessori Egg Puzzle Toys due to a choking hazard. The recalled toys are intended for children under three years of age and the eggs can block a child's airway, posing a risk of choking and death to children.

    Product
    TheKiddoSpace Children's Montessori Egg Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26286·2026-02-26

    Tubby Tots Fizzy Flask Bath Magic Bath Foam Sets Recalled for Impact Hazard

    Surreal Brands is recalling Tubby Tots Fizzy Flask Bath Magic bath foam sets because moisture can build up pressure in the container, causing pieces to eject forcefully.

    Product
    Tubby Tots Fizzy Flask Bath Magic bath foam set
    Category
    Consumer Product
    Distribution
    Distributed nationwide