The Recall Desk

State

Georgia product recalls

73,741 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,632
Critical
1,471
Severe
2,565
Most recent
2026-10-28

Of the 9,632 recalls naming Georgia we have scored against our rubric, 1,471 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,565 (27%) are Severe.

These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38676–38700 of 83373

  • SevereNHTSA·19V314000·2019-04-18

    Mercedes-Benz Recalls 2019 A 220 Vehicles Due to Brake Pedal Welding Defect

    Mercedes-Benz is recalling 2019 A 220 and A 220 4MATIC vehicles because improper welding may cause the pedal plate to bend, impairing brake pedal operation and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E030000·2019-04-18

    Bendix Recalls Air Disc Brake Calipers for School Buses

    Bendix is recalling ADB22X Air Disc Brake Calipers for school buses because the driver side rear brakes may drag, increasing the risk of fire.

    Product
    SERVICE BRAKES, AIR:DISC recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19107·2019-04-18

    Tekno Recalls Tuff Smoke-Less Grills Due to Fire and Burn Hazards

    Tekno Products is recalling Tuff smoke-less grills because they can overheat, posing fire and burn hazards. Consumers should stop using the grills and return them for a refund.

    Product
    Tuff smoke-less grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V312000·2019-04-18

    GM Recalls 2017-2019 Chevrolet Trax for Front Suspension Weld Defect

    General Motors is recalling 2017-2019 Chevrolet Trax vehicles because improperly welded front lower-control arm joints may break, causing partial separation and increased crash risk.

    Product
    CHEVROLET — CHEVROLET TRAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V309000·2019-04-18

    2019 Mercedes-Benz Sprinter Recalled for High-Beam Software Error

    Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vans because a software error may prevent drivers from turning off high beams, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V316000·2019-04-18

    Nissan Recalls 2019 Altima Vehicles Due to Fuel Pump Lock Ring Defect

    Nissan is recalling 2019 Altima vehicles with front-wheel drive and 2.5-liter engines because a fuel pump lock ring may not be fully engaged, potentially causing a fuel leak and fire risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19108·2019-04-18

    Target Recalls Wooden Toy Vehicles Due to Choking Hazard

    Target is recalling Bullseye's Playground wooden toy vehicles because wheels can detach, posing a choking hazard to children.

    Product
    Bullseye's Playground wooden toy vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19739·2019-04-18

    RH Recalls Callum Canopy Beds Due to Falling Rail Injury Hazard

    RH is recalling Callum Canopy Beds because horizontal canopy rails can detach and fall. No injuries have been reported, but consumers should stop using the beds until repaired.

    Product
    Callum Canopy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V313000·2019-04-18

    MobilityTrans Recalls Modified Ford and Ram Vans with Defective Foldaway Seats

    Mobility Transportation Services is recalling modified Ford and Ram vans because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    FORD — FORD, RAM, MOBILITY SPECIALISTS E-350, E-250, PROMASTER, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1135-2019·2019-04-17

    FDA Recalls Leopard Miracle Honey Containing Undeclared Sildenafil

    USA LESS Inc. is recalling Leopard Miracle Honey because it contains undeclared sildenafil, an unapproved drug for erectile dysfunction.

    Product
    LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1 Sachet 15 gr / 0.53 Oz is labeled as LEOPARD Miracle of Honey, UPC 8 699415 912859, Manufactured in Turkey, www leopardhoneytr.com.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1300-2019·2019-04-17

    Theo Chocolate Sea Salt 70% Dark Chocolate Bars Recalled for Undeclared Milk

    Theo Chocolate is recalling Sea Salt 70% Dark Chocolate bars due to undeclared milk. The product was distributed nationwide.

    Product
    Sea Salt 70% Dark Chocolate 3 oz. bars, wrapped in foil and paper wrapper, brand Theo Chocolate, UPC 8 74492 00325 8. The Sea Salt 70% Dark Chocolate 3 oz. bar's label is read in part: "***Sea Salt 70% Dark Chocolate *** Ingredients: Cocoa Beans, Cane Sugar, Sea Salt, Ground…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1118-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA testing found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/12.5mg, a) 30-count (NDC: 13668-117-30), b) 90-count (NDC: 13668-117-90) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1123-2019·2019-04-17

    Encore Medical Recalls Exprt Precision System Hip Implant Components

    Encore Medical is recalling 22 units of Exprt Precision System hip implant components due to loose or improperly seated bolts that may cause pain or require revision surgery.

    Product
    Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF: 495-00-065, 495-00-075, 495-00-085, 495-01-065, 495-01-075, 495-01-085
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Drugs)·D-1117-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 50mg/12.5mg, a) 30-count (NDC: 13668-116-30), b) 90-count (NDC: 13668-116-90), c) 1000-count (NDC: 13668-116-10) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1119-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/25mg, a) 30-count (NDC: 13668-118-30), b) 90-count (NDC: 13668-118-90), c) 1000-count (NDC: 13668-118-10) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1273-2019·2019-04-17

    Almark Foods Recalls Hard-Boiled Eggs Due to Listeria Test Results

    Almark Foods is recalling 20-pound pails of Nic's Peeled Pearls hard-boiled eggs after FDA notified the firm of positive Listeria monocytogenes test results.

    Product
    Nic's Peeled Pearls 20lb. Salad Grade Hard-Boiled Eggs NET WT. WHEN PACKED 20lbs Manufactured By: Almark Foods Gainesville, GA 30504 1.800.849.EGGS
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1111-2019·2019-04-17

    McDaniel Life-Line Recalls Indian Herb Paste Due to Unapproved New Drug Status

    McDaniel Life-Line LLC is voluntarily recalling 150 vials of Indian Herb Paste because the product is an unapproved new drug. The recall covers distribution in the US, Italy, Australia, Canada, and Poland.

    Product
    Indian Herb Paste (a dietary supplement) Ingredients: Galangal, Indian Paint, Yellow Dock & Licorice in an alloy of Life-Line tm and Zinc Chloride in 6 dram vials, McDaniel Life-Line LLC, Dimmitt, TX
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1114-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 25 mg, because FDA labs found an impurity above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 25 mg, a) 90-count (NDC: 13668-113-90), b) 1000-count (NDC: 13668-113-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V311000·2019-04-17

    Hyundai Recalls 2019 Veloster Vehicles Due to Door Latch Defect

    Hyundai is recalling 12,438 2019 Veloster vehicles because the driver's door latch can fail in a side impact crash, potentially allowing the door to open.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1116-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 100 mg, because FDA testing found an impurity above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 100 mg, a) 90-count (NDC: 13668-115-90), b) 1000-count (NDC: 13668-115-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen Road, Suite 102, Basking…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1115-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium Tablets, 50 mg, because FDA testing found an impurity above acceptable levels.

    Product
    LOSARTAN POTASSIUM TABLETS, USP, 50 mg, a) 30-count (NDC: 13668-409-30), b) 90-count (NDC: 13668-409-90), c) 1000-count (NDC: 13668-409-10), per bottle, Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V304000·2019-04-17

    Spartan Recalls 2019 Utilimaster Truck Bodies Due to Electrical Fire Risk

    Spartan Motors is recalling 2019 Utilimaster Truck Bodies because undersized wires may overheat, melt, and cause an unexpected engine shutdown, increasing crash risk.

    Product
    UTILIMASTER — UTILIMASTER TRUCK BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide