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.

38201–38225 of 83373

  • SevereNHTSA·19V393000·2019-05-24

    Blue Bird Recalls Buses Due to Rear Brake Dragging Risk

    Blue Bird is recalling certain 2015-2020 Vision and All American non-school buses because driver-side rear brakes may drag, posing a fire and injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V391000·2019-05-24

    Blue Bird Recalls School Buses Due to Rear Brake Dragging Risk

    Blue Bird is recalling 2015-2020 Vision and All American school buses because the driver-side rear brakes may drag, posing a fire and injury risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, ALL AMERICAN SCHOOL BUS, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V395000·2019-05-24

    Starcraft All Star XL Diesel Fuel Heater Fire Risk Recall

    Forest River is recalling 2018-2019 Starcraft All Star XL diesel vehicles because the fuel heater may overheat, melt plastic, and cause a fire or engine stall.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V392000·2019-05-24

    Land Rover Recalls Range Rover Models for Door Latch Defect

    Jaguar Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may appear closed but are unlatched, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E036000·2019-05-23

    Meritor recalls steer axles due to insufficient lubrication risk

    Meritor is recalling specific steer axles because insufficient lubrication may damage wheel end bearings, potentially causing wheel separation and loss of vehicle control.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E035000·2019-05-23

    Transfer Flow Recalls Rear Brake Lines for Mobility Van Conversions

    Transfer Flow is recalling rear brake lines for mobility van conversions due to incorrect tube nut fittings that may cause a pressure drop in the braking system.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V386000·2019-05-23

    BMW Recalls 2019 X7 Vehicles Due to Head Air Bag Alignment Defect

    BMW is recalling 2019 X7 xDrive40i and xDrive50i vehicles because the driver and passenger head air bags may not be properly aligned, potentially impairing deployment and increasing injury risk.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V387000·2019-05-23

    GM Recalls 2016-2019 Chevrolet Express and GMC Savana for Window Glass Defect

    General Motors is recalling 2016-2019 Chevrolet Express and GMC Savana vehicles because rear-quarter windows may use tempered glass instead of laminated glass, increasing injury risk in crashes.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V390000·2019-05-23

    Land Rover Recalls 2016 Range Rovers for Door Latch Defect

    Jaguar Land Rover is recalling 28,671 2016 Range Rover and Range Rover Sport vehicles because a stuck spring may leave the left door unlatched, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19127·2019-05-23

    DICK'S Sporting Goods Recalls Ethos Pull-Up Assist Due To Laceration Hazard

    DICK'S Sporting Goods is recalling Ethos Pull-Up Assist equipment because a plastic clip can break, posing a laceration hazard. Seven reports of equipment breaking resulted in six lacerations.

    Product
    Ethos Pull-Up Assist
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19125·2019-05-23

    Far East Brokers Recalls Fabulous Home Pineapple Corer and Slicers

    Far East Brokers is recalling Fabulous Home Pineapple Corer & Slicers because the metal blade can detach, posing a laceration hazard.

    Product
    Fabulous Home Pineapple Corer & Slicers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·058-2019·2019-05-23

    Blount Fine Foods Recalls Chicken Tortilla Soup Due to Plastic Contamination

    Blount Fine Foods is recalling specific lots of Panera Bread at Home Chicken Tortilla Soup due to possible plastic contamination. No illnesses have been reported.

    Product
    Blount Fine Foods Corp. — Blount Fine Foods Recalls Soup with Chicken Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-1292-2019·2019-05-22

    Titanium 4000 capsules recalled for undeclared sildenafil and tadalafil

    D.B.P. Distribution is recalling Titanium 4000 capsules because they contain undeclared sildenafil and tadalafil and were marketed without an approved NDA or ANDA.

    Product
    Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000 UPC 86077000020
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1275-2019·2019-05-22

    Ethicon Intraluminal Staplers Recalled for Insufficient Firing Stroke

    Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH21A) because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Straight Intraluminal Staplers, 21 mm diameter, Model SDH21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1273-2019·2019-05-22

    Ethicon Endo-Surgery Recalls Endoscopic Curved Intraluminal Staplers

    Ethicon Endo-Surgery is recalling 434,614 endoscopic curved intraluminal staplers because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Endoscopic Curved Intraluminal Stapler, 29 mm diameter, Model ECS29A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1277-2019·2019-05-22

    Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect

    Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Straight Intraluminal Staplers, 29 mm diameter, Model SDH29A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1278-2019·2019-05-22

    Ethicon Endo-Surgery Recalls Straight Intraluminal Staplers Due to Firing Defect

    Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH33A) because they may have an insufficient firing stroke to break the washer and completely form staples.

    Product
    Straight Intraluminal Staplers, 33 mm diameter, Model SDH33A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1351-2019·2019-05-22

    Molift 2-Point Sling Bar Recalled Due to Hook Breakage Risk

    Moller Vital is recalling 427 Molift 2-Point sling bars because broken hooks may cause the sling to slip, potentially leading to patient falls.

    Product
    Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
    Category
    Medical Device
    Distribution
    10 states