The Recall Desk

State

Georgia product recalls

72,940 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,588
Critical
1,464
Severe
2,164
Most recent
2026-09-09

Of the 9,588 recalls naming Georgia we have scored against our rubric, 1,464 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,164 (23%) are Severe.

These figures cover only the 9,588 recalls whose distribution notice names Georgia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3701–3725 of 82528

  • HighNHTSA·26V043000·2026-01-23

    2026 Brinkley RV Model Z Trailers Recalled for Fire Risk

    Brinkley RV is recalling certain 2026 Model Z trailers because shore power inlet lugs may be improperly tightened, causing wires to loosen, overheat, and create a fire hazard.

    Product
    BRINKLEY RV — BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26215·2026-01-22

    Semi electric homecare beds recalled over hand pendants that may overheat

    Medline is recalling 373,392 units of the Semi Electric Basic Homecare Bed because the hand control pendant and its cords may overheat and, in rare instances, pose a risk of fire.

    Product
    Mikario Trading 5-in-1 Convertible Baby Gyms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V031000·2026-01-22

    Chevrolet Blazer EV parking brake may activate unintentionally or fail

    GM is recalling certain 2024-2025 Chevrolet Blazer EV vehicles that may have been repaired incorrectly under recall 25V433, because the rear parking brake wiring harness may become damaged or corroded.

    Product
    CHEVROLET — CHEVROLET BLAZER EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26204·2026-01-22

    Pull string teething toys recalled over silicone strings that can lodge

    About 6,800 Yetonamr Pull String Teething Toys are being recalled because the silicone strings can reach the back of the throat and become lodged. CPSC is aware of 32 choking incidents.

    Product
    Yetonamr Pull String Teething Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26208·2026-01-22

    Magnetic stick figure toy sets recalled over loose ingestible magnets

    About 1,600 Vndueey Magnetic Men toy sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.

    Product
    Vndueey Magnetic Men Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26203·2026-01-22

    Treadmills recalled over power cords that can loosen from the socket

    About 47,000 Matrix and Vision treadmills are being recalled because the power cord can become loose from the power socket, posing a fire hazard.

    Product
    Matrix Retail T30, TF30, T50, TF50, and T75 treadmills, Vision T9800, TF20, T40, and T80 treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26206·2026-01-22

    Torch lighters recalled over a lack of child-resistant mechanisms

    About 7,500 Topkay Torch Lighters are being recalled because they do not have the child-resistant mechanisms required by the mandatory standard for multipurpose lighters.

    Product
    Topkay Torch Lighters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26202·2026-01-22

    Folding rocker chairs recalled over legs that can break

    About 35,300 Magellan Odyssey Rocker Chairs sold by Academy Sports + Outdoors are being recalled because the chairs' legs can break.

    Product
    Magellan Odyssey Rocker Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26207·2026-01-22

    Fidget magnet ball toys recalled over loose high-powered magnets

    About 9,300 Based Online Fidget Magnet Ball Toy Sets are being recalled because they contain magnets that can be swallowed by children. CPSC reports no injuries or incidents.

    Product
    Based Online Fidget Magnet Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V033000·2026-01-22

    Blue Bird Recalls One 2026 Vision Transit Bus for Window Markings

    Blue Bird is recalling one 2026 Vision transit bus because side or rear windows may have illegible DOT markings, failing federal safety standards.

    Product
    BLUE BIRD — BLUE BIRD VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V032000·2026-01-22

    Blue Bird Recalls 2026-2027 School Buses for Illegible Window Markings

    Blue Bird is recalling 2026-2027 Vision and All American school buses because side and rear windows may have illegible DOT markings, failing federal safety standards.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0404-2026·2026-01-21

    Ayurvedic gastro supplement recalled over potential undeclared wheat

    Herbs Forever is recalling 45 units of HerbsForever Gastro Care Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The FDA has classified the action as Class I.

    Product
    HerbsForever- Gastro Care; Ayruvedic Herbal Supplement; 90 VEGE Capsules; Extract 800 MG each capsule. UPC: 8 07814 00124 3
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0405-2026·2026-01-21

    Hingwastika churna supplement recalled over potential undeclared wheat

    Herbs Forever is recalling 45 units of HerbsForever Hingwastika Churna Ayurvedic Herbal Supplement over a potential undeclared allergen, wheat. The action is Class I.

    Product
    HerbsForever- Hingwastika Churna ; Ayruvedic Herbal Supplement; 90 VEGE Capsules; 100 GMS UPC: 8 07814 00622 4
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1021-2026·2026-01-21

    Libre 3 Plus sensors recalled in a second lot over carbon build up

    Abbott Diabetes Care is recalling 1,663,241 FreeStyle Libre 3 Plus sensors, REF 78768-01, because carbon build up in the sensor may result in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 78768-01 UDI-DI code: 00357599844011 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1052-2026·2026-01-21

    Holiday cookie tins recalled over undeclared almond, pecan and walnut

    One Roof LLC is recalling 197 Atwater's Holiday Cookie Tins over undeclared tree nut allergens: almonds, pecans and walnuts.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) RR-LE FORT MANDIBLE PACK-LF, Medline Kit SKU DYNJ0785864R; 2) RR-ASC EAR PACK-LF, Medline Kit SKU DYNJ0792607R.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1020-2026·2026-01-21

    Glucose monitoring sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 1,060,723 FreeStyle Libre 3 sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Sensor REF 72081-01 UDI-DI code: 00357599818005 The FreeStyle Libre 3 sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1023-2026·2026-01-21

    Libre 3 Plus sensors recalled over carbon build up causing low readings

    Abbott Diabetes Care is recalling 8,062 FreeStyle Libre 3 Plus sensors because a manufacturing process issue may cause carbon build up that results in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 72080-01 UDI-DI code: 00357599819002 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states
  • CriticalFDA (Devices)·Z-1022-2026·2026-01-21

    Libre 3 Plus sensors, REF 78769-01, recalled over carbon build up

    Abbott Diabetes Care is recalling 258,913 FreeStyle Libre 3 Plus sensors, REF 78769-01, because carbon build up in the sensor may result in incorrect low glucose results.

    Product
    FreeStyle Libre 3 Plus Sensor REF 78769-01 UDI-DI code: 00357599843014 The FreeStyle Libre 3 Plus sensor is a component of the FreeStyle Libre 3 Continuous Glucose Monitoring System.
    Category
    Medical Device
    Distribution
    36 states