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.

39501–39525 of 83373

  • ModerateFDA (Drugs)·D-1012-2019·2019-03-20

    Medtech Recalls Little Remedies New Baby Essentials Kit for Labeling Errors

    Medtech Products is recalling 4,716 Little Remedies New Baby Essentials Kits because the cartons contain incorrect labeling for two of the five items inside.

    Product
    Little Remedies New Baby Essentials Kit. Each kit contains 1 each of the following products: Little Remedies Infant Fever Reducer (acetaminophen 150mg) 2 fl. oz. bottle, Little Remedies Saline Spray/Drops (sodium chloride) 0.5 fl oz., Little Remedies Gripe Water (zingiber…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1004-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications. The recall covers 140,589 bottles distributed nationwide.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets, USP 80mg/12.5 mg, 30-coun bottles, Rx Only, Manufactured for: Macleods Pharma USA, Inc. Plainsboro, NJ 08536 Manufactured by: Macleods Pharmaceuticals Ltd. Baddi, Imachal Pradesh, India NDC 33342-129-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1001-2019·2019-03-20

    Ossur Halo System Ring Kits Recalled for Labeling and Safety Testing

    Ossur Americas is recalling 182 units of Halo system ring kits due to a labeling error and the need for confirmatory safety testing.

    Product
    Ossur, Sterile, Part/ Description: 505300T/ CB RING KIT TI SM; 505300V2/ OB V2 RING KIT TI SM; 505400T/ CB RING KIT TI STD; 505400V2/ OB V2 RING KIT TI STD; 505500T/ CB RING KIT TI LG; 505500V2/ OB V2 RING KIT TI LG; 515300V2/ OB V2 RING KIT TI SM-No App; 515400V2…
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Drugs)·D-1003-2019·2019-03-20

    Macleods Pharma Recalls Telmisartan and Hydrochlorothiazide Tablets for Blend Uniformity

    Macleods Pharma USA is recalling Telmisartan and Hydrochlorothiazide tablets because they failed blend uniformity specifications.

    Product
    Telmisartan and Hyrdochlorothiazide Tablets 40mg/12.5 mg, 30-count bottles, Rx Only, Manufactured for:Macleods Pharma USA, Inc. Plainsboro, NJ 08536, Manufactured for: Macleods Pharmaceuticals Ltd. Baddi, Himchal Pradesh INDIA, NDC 33342-128-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1005-2019·2019-03-20

    Zimmer NexGen Trabecular Metal Tibial Augment Recall for Label Mismatch

    Zimmer Trabecular Metal Technology is recalling 24 units of NexGen Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Right Lateral/Left Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800426 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1007-2019·2019-03-20

    Olympus Ultrasound Gastrovideoscope Recalled Due to Adhesive Preparation Error

    Olympus is recalling one ultrasound gastrovideoscope because the adhesive used for its repair was incorrectly prepared, potentially affecting the device's durability.

    Product
    Olympus GF-UCT180 Ultrasound Gastrovideoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0991-2019·2019-03-20

    Boehringer Ingelheim Recalls Mirapex Tablets Due to Low Weight

    Boehringer Ingelheim is recalling 112 cartons of Mirapex 1 mg tablets because routine stability testing identified low-weight tablets.

    Product
    Mirapex (pramipexole dihydrochloride) Tablets, 1 mg, 100-count unit-dose tablets per folding carton, Rx only, Distributed by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877 USA, Made in Germany, NDC 0597-0190-61.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·19V211000·2019-03-19

    Collins Recalls 2015-2019 School Buses Due to Barrier Restraint Defect

    Collins Bus is recalling 2015-2019 school buses because a specific barrier may fail to restrain unbelted occupants during a crash, increasing injury risk.

    Product
    COLLINS — COLLINS DH400, DH516, DE500, DE416
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V212000·2019-03-19

    Alexis Fire Equipment Recalls 2018 Fire Apparatus Due to Brake Light Defect

    Alexis Fire Equipment is recalling 11 units of 2018 Custom Fire Apparatus because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V209000·2019-03-18

    Mack Trucks Recalls 2020 Models Due to Blocked Rear Reflectors

    Mack Trucks is recalling 2020 Anthem and Pinnacle trucks because exhaust systems may block rear reflectors, reducing vehicle visibility.

    Product
    MACK — MACK ANTHEM (AN), PINNACLE (PI/PN), PINNACLE (CHU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V206000·2019-03-18

    Keystone Recalls 2019 Dutchmen Trailers Due to Cooktop Burn Hazard

    Keystone RV is recalling 2019 Dutchmen Coleman and Aspen Trail trailers because the cooktop may cause excessive heat buildup and burns when the furnace is on.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN, ASPEN TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19728·2019-03-14

    Kawasaki Recalls Mule Pro-MX Utility Vehicles Due to Fuel Leak Fire Hazard

    Kawasaki is recalling about 2,600 Mule Pro-MX off-highway utility vehicles because oil cooler hoses and fuel tank cap gaskets can fail, causing fuel leaks and fire hazards.

    Product
    Kawasaki Mule™ Pro-MX™ off-highway utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V204000·2019-03-14

    Hyundai Recalls 2013 Veloster Vehicles Due to Engine Software Defect

    Hyundai is recalling 2013 Veloster vehicles with 1.6-liter turbo engines because software may cause premature ignition, risking engine damage, fire, or stalling.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V201000·2019-03-14

    Chrysler Recalls 2019 Jeep Wrangler and Ram 1500 for Steering Defect

    Chrysler is recalling 2019 Jeep Wrangler and Ram 1500 vehicles because improperly machined steering column stub shafts may break, potentially causing the steering wheel to detach.

    Product
    JEEP — JEEP, RAM WRANGLER, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19082·2019-03-14

    Tech Gear 5.7 Recalls Heated Socks Due to Fire and Burn Hazards

    Tech Gear 5.7 is recalling Mobile Warming Performance Heated Socks because the lithium-ion battery can overheat, melt, or ignite, posing fire and burn risks.

    Product
    Mobile Warming Performance Heated Socks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V200000·2019-03-14

    Thor Motor Coach Recalls 2018-2019 Aria and Palazzo Motorhomes

    Thor Motor Coach is recalling 2018-2019 Aria and 2019 Palazzo motorhomes because loose steering and tie rod arm bolts may separate, increasing crash risk.

    Product
    THOR — THOR PALAZZO, ARIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19083·2019-03-14

    O'Brien Performer Pro Combo Water Skis Recalled for Injury Hazard

    O'Brien Watersports is recalling Performer Pro Combo water skis because the bindings can detach during falls, causing the skis to break and injure users.

    Product
    Performer Pro Combo water skis
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V203000·2019-03-14

    Chrysler Recalls 2019 Models for Instrument Cluster Illumination Defect

    Chrysler is recalling 2019 Dodge Challenger, Charger, and Chrysler 300 vehicles because the instrument cluster may fail to illuminate driver warnings, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER, DODGE 300, CHARGER, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide