The Recall Desk

State

Georgia product recalls

73,817 recalls have nationwide distribution and so reach Georgia. 9,635 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,635
Critical
1,471
Severe
2,567
Most recent
2026-11-04

Of the 9,635 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 2,567 (27%) are Severe.

These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49976–50000 of 83452

  • HighNHTSA·17V239000·2017-04-10

    Thor Motor Coach Recalls 2017 Motorhomes Due to Incorrect Hitch Weight Labels

    Thor Motor Coach is recalling 2017 Ace, Hurricane, and Windsport motorhomes because tow hitch labels incorrectly state a 10,000 lb capacity instead of the actual 8,000 lbs.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR WINDSPORT, HURRICANE, ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V244000·2017-04-10

    Mercedes-Benz Recalls 2016 Metris for Front Seatbelt Pretensioner Defect

    Daimler Vans USA is recalling 2016 Mercedes-Benz Metris vehicles because front seatbelt pretensioners may not function properly in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V238000·2017-04-10

    Thor Motor Coach Recalls 2017 Palazzo Motorhomes for Incorrect Tire Labeling

    Thor Motor Coach is recalling 2017 Palazzo 36.1 and 36.3 motorhomes because the federal certification label lists an incorrect front tire rim size, which could lead to unsafe driving conditions if the rim is replaced based on that error.

    Product
    THOR — THOR PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V236000·2017-04-07

    Altec Recalls 2004-2005 Aerial Devices Due to Boom Failure Risk

    Altec is recalling 2004-2005 aerial devices and elevators because the fiberglass upper boom may fail without warning, increasing the risk of serious injury or death.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V237000·2017-04-07

    Forest River Cherokee Recalled for Incorrect Federal Placard Weight Ratings

    Forest River is recalling 2007-2011 Cherokee recreational trailers because incorrect Federal Placards list higher weight ratings than the actual capacity, increasing the risk of overloading and crashes.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V233000·2017-04-06

    Mitsubishi Recalls 2016 Outlander Models for Door Latch Defect

    Mitsubishi is recalling 35,674 2016 Outlander and Outlander Sport vehicles because door latches may not secure in high temperatures, increasing injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V234000·2017-04-06

    Micro Bird Recalls 2016-2017 G5 School Buses for Fuel Valve Defect

    Micro Bird is recalling 2016-2017 G5 school buses with specific propane kits because a fuel valve may short circuit, causing the engine to shut off while driving.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17126·2017-04-06

    Marin Pine Mountain Bicycles Recalled Due to Fork Failure Hazards

    Marin Mountain Bikes is recalling 2016 and 2017 Pine Mountain bicycles because the front forks can bend or break, posing fall and crash hazards.

    Product
    Pine Mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1721-2017·2017-04-05

    FDA Recalls Ruth's Lite Pimento Spread Due to Listeria Risk

    B & H Foods is recalling 2,776 units of Ruth's Lite Pimento Spread because the product may be contaminated with Listeria monocytogenes.

    Product
    Ruth's Lite Pimento Spread, 12 oz. (UPC 74952-12000), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic containers.
    Category
    Food
    Distribution
    6 states
  • CriticalFDA (Food)·F-1777-2017·2017-04-05

    Saputo Recalls Dutchmark Smoked Gouda Cheese Due to Listeria Risk

    Saputo Cheese USA is recalling Dutchmark Smoked Gouda Cheese because it may be contaminated with Listeria monocytogenes.

    Product
    Dutchmark, Pasteurized Processed Smoked Gouda Cheese. Product case Label: 989922 Dutchmark, Net Wt 24.00.
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Devices)·Z-1417-2017·2017-04-05

    Philips HeartStart MRx Monitor/Defibrillator Recalled for Potential Failure to Deliver Therapy

    Philips is recalling HeartStart MRx Monitor/Defibrillators because they may fail to deliver therapy or monitoring when operating on a single battery.

    Product
    HeartStart MRx Monitor/Defibrillator, Model numbers: M3535A (M3535ATZ) M3536A (M3536ATZ), M3536M, M3536MC, M3536M2, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, M3536M9
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1720-2017·2017-04-05

    B & H Foods Recalls Ruth's Jalapeno Pimento Spread for Listeria Risk

    B & H Foods is recalling 3,394 units of Ruth's Jalapeno Pimento Spread due to potential Listeria monocytogenes contamination. The product was distributed in six southeastern states.

    Product
    Ruth's Jalapeno Pimento Spread, 12 oz. (UPC 74952-12014), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic containers.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0616-2017·2017-04-05

    Claris Recalls Metronidazole Injection Due to Sterility Concerns

    Claris Lifesciences Inc. is recalling 72,072 units of Metronidazole Injection, USP, 500 mg/100 mL, due to a potential leak that may compromise sterility.

    Product
    Metronidazole Injection, USP, 500 mg/100 mL, Rx only, Manufactured for: Claris Lifesciences Inc. North Brunswick NJ, 08902, By: Claris Injectable Ltd. Gujarat, India, NDC 36000-001-24
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1718-2017·2017-04-05

    B & H Foods Recalls Ruth's Pimento Spread for Listeria Risk

    B & H Foods is recalling Ruth's Original Pimento Spread in 7oz, 12oz, and 24oz sizes due to potential Listeria monocytogenes contamination. The product was distributed in six southeastern states.

    Product
    Ruth's Original Pimento Spread 7oz (UPC 74952-0005), 12oz (UPC 74952-12023) and 24oz (74952-24023), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic containers.
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·17V231000·2017-04-05

    E-One Recalls Emergency Vehicles Due to Front Suspension Ball Joint Defect

    E-One is recalling 2013-2016 Quest, Typhoon, and Cyclone II emergency vehicles because front suspension ball joints can loosen and separate, potentially causing a loss of steering control.

    Product
    E-ONE — E-ONE QUEST, TYPHOON, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0618-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Pharmaceuticals is recalling specific lots of Atorvastatin Calcium 10 mg tablets due to potential microbial contamination and elevated bioburden.

    Product
    Atorvastatin Calcium Tablets, 10 mg*, packaged in a) 90-count bottles (NDC 0378-3950-77); b) 90-count bottles (NDC 0378-3950-09); c) 500-count bottles (NDC 0378-3950-05); d) 500-count bottles (NDC 0378-3950-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1497-2017·2017-04-05

    Merit Medical Recalls 7F Prelude Short Sheath Introducers Due to Detachment Risk

    Merit Medical Systems is voluntarily recalling 1,265 units of 7F Prelude Short Sheath Introducers because the sheath marker tips may detach during use.

    Product
    7F Prelude¿ Short Sheath Introducer. Catalog Numbers: K15-00070, K15-00170, PSS-7F-4-035MT, PSS-7F-4MT. Produc Usage: The Merit Prelude¿ Short Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1719-2017·2017-04-05

    B & H Foods Recalls Pimento Spread for Listeria Risk

    B & H Foods is recalling Ruth's Old Fashion Pimento Spread due to potential Listeria monocytogenes contamination. The product was distributed in six southeastern states.

    Product
    Ruth's Old Fashion Pimento Spread, 16oz. (UPC 74952-15005), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic containers.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1722-2017·2017-04-05

    B & H Foods Recalls Ruth's Cream Cheese for Listeria Risk

    B & H Foods is recalling 459 units of Ruth's Cream Cheese w/Pineapple-Pecans due to potential Listeria monocytogenes contamination. The product was distributed in six southeastern states.

    Product
    Ruth's Cream Cheese w/Pineapple-Pecans, 12 oz. (UPC 74952-12008), Packed By: B & H Foods, 181 Saluda ST, Chester, SC 29706, packed in plastic containers.
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0621-2017·2017-04-05

    Mylan Recalls Atorvastatin Calcium Tablets Due to Microbial Contamination

    Mylan Pharmaceuticals is recalling Atorvastatin Calcium Tablets, 80 mg, due to potential microbial contamination and elevated bioburden.

    Product
    Atorvastatin Calcium Tablets, 80 mg*, packaged in a) 90-count bottles (NDC 0378-3953-09) and b) 500-count bottles (NDC 0378-3953-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide