The Recall Desk

State

Georgia product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42676–42700 of 83444

  • SevereNHTSA·18E081000·2018-08-10

    Cummins Recalls Diesel Engines Due to Fuel Line Burst Risk

    Cummins is recalling ISX15 and X15 diesel engines because a restricted fuel pump screen can cause the nylon fuel line to burst, leading to fuel leaks or engine stalling.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V526000·2018-08-10

    KZRV Sportsmen Travel Trailers Recalled for Propane Line Fire Risk

    KZRV is recalling 2018-2019 Sportsmen 333BHK travel trailers because liquid propane lines routed through the wheel well may be damaged by road debris, increasing fire risk.

    Product
    KZRV — KZRV SPORTSMEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E080000·2018-08-09

    TRW Recalls Outer Tie Rods for Loss of Steering Risk

    TRW is recalling specific outer tie rods sold as replacement parts for 1988-2000 GM vehicles because the locking nut may fail, causing a loss of steering.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V525000·2018-08-09

    Freightliner Trucks Recalled for Insufficiently Tightened Brake Caliper Bolts

    Daimler Trucks North America is recalling 2018-2019 Freightliner trucks because brake caliper mounting bolts may be loose, which can reduce braking effectiveness and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER 108SD, 114SD, CASCADIA, 122SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V523000·2018-08-09

    Chrysler Recalls 2018-2019 Vehicles for Rear Brake Caliper Coating Defect

    Chrysler is recalling specific 2018-2019 Dodge and Jeep vehicles because rear brake caliper pistons may have insufficient coating, potentially reducing braking performance.

    Product
    DODGE — DODGE, JEEP GRAND CARAVAN, CHEROKEE, JOURNEY, COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V524000·2018-08-09

    Chrysler, Jeep, and Ram Vehicles Recalled for Powertrain Control Module Defect

    FCA US LLC is recalling specific 2017-2019 Chrysler, Jeep, Ram, Dodge, and Fiat vehicles because a faulty voltage regulator chip may cause the vehicle to stall or fail to start.

    Product
    CHRYSLER — CHRYSLER, RAM, JEEP PACIFICA PLUG-IN HYBRID, PACIFICA, 1500, RENEGADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18202·2018-08-09

    Vitamix Recalls Ascent and Venturist Blending Containers Due to Laceration Hazard

    Vitamix is recalling Ascent and Venturist series blending containers because they can separate from the blade base, exposing blades and posing a laceration hazard.

    Product
    Ascent™ and Venturist™ Series 8-ounce and 20-ounce blending containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V511000·2018-08-09

    Gillig Recalls Low Floor Buses Due to Turn Signal Flashing Defect

    Gillig is recalling 2012-2018 Low Floor buses because front and rear turn signals may flash at different rates, potentially confusing other drivers.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1675-2018·2018-08-08

    Probiotic Supplement Recalled for Potential Undeclared Allergens

    LL'S Magnetic Clay Inc. is recalling Prescript-Assist Probiotic & Prebiotic supplements because they may contain undeclared almonds, shellfish, milk, eggs, or peanuts.

    Product
    Prescript-Assist Broad Spectrum Probiotic & Prebiotic Gastrointestinal Support Dietary Supplement, 60-capsule or 90-capsule bottles; UPC Codes: 853956003157, 853956003539
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1802-2018·2018-08-08

    Sugar Foods Recalls Cheese Garlic Croutons Due to Whey Powder Contamination

    Sugar Foods Corporation is recalling HMS Cheese Garlic Croutons because they were produced using recalled whey powder.

    Product
    HMS Cheese Garlic Croutons: 2.5 lb. foil pouch Item # 74906 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2559-2018·2018-08-08

    Galt Medical Recalls Vascular Dilators and Introducer Kits Due to Endotoxins

    Galt Medical Corporation is recalling specific vascular dilators and introducer kits because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    1) Vascular Dilator, Sterile EO, Rx Only, Catalog #: DIL-100-12; 2) Dilator, Sterile EO, Rx Only, Catalog #: DIL-600-11; 3) Tearaway Introducer, Sterile EO, Rx Only, Catalog #: a) INT-028-14; b) INT-028-24; c) INT-029-05; d) INT-106-01; e) INT-106-14; 4) Micro-Access…
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Devices)·Z-2558-2018·2018-08-08

    Galt Medical Recalls Sterile Hemostasis Valve Introducer Systems Due to Endotoxins

    Galt Medical Corporation is recalling specific sterile hemostasis valve introducer systems and kits because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c) BCL-100-06; d) BCL-500-36; 2) Elite HV Introducer Set, Sterile EO, Rx Only, Catalog #: a) CLI-105-14; 3) AngioGate HV Introducer Kit, Sterile EO, Catalog #…
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Food)·F-1800-2018·2018-08-08

    Sugar Foods Recalls Seasoned Croutons Due to Whey Powder Contamination

    Sugar Foods Corporation is recalling First Street Restaurant Style Seasoned Croutons because they were made with recalled whey powder.

    Product
    First Street Restaurant Style Seasoned Croutons: 24 oz. foil pouch Item # 31424 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1805-2018·2018-08-08

    Sugar Foods Recalls Sizzler Seasoned Croutons Due to Whey Powder Contamination

    Sugar Foods Corporation is recalling Sizzler HMS Seasoned Croutons because they were made with recalled whey powder. The product was distributed in six states.

    Product
    Sizzler HMS Seasoned Croutons: 2.5 lb. foil pouch Item # 74803 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1807-2018·2018-08-08

    Sugar Foods Croutons Recalled Due to Contaminated Whey Ingredient

    Sugar Foods Corporation is recalling seasoned croutons because they were made with recalled whey powder.

    Product
    Classic Sysco cube seasoned croutons: 0.25 oz. plastic pouch Item # 20602 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-2563-2018·2018-08-08

    Galt Medical Recalls Centeze Centesis Catheters Due to Bacterial Endotoxins

    Galt Medical Corporation is recalling 300 units of Centeze Centesis Catheters because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    Centeze Centesis Catheter, Catalog #: a) DRC-006-05, b) DRC-006-15,
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Food)·F-1798-2018·2018-08-08

    Sugar Foods Recalls Homestyle Seasoned Croutons Due to Whey Powder Contamination

    Sugar Foods Corporation is recalling 4 oz. pouches of Homestyle Seasoned Croutons because they were produced using recalled whey powder.

    Product
    Homestyle Seasoned Croutons: 4 oz. foil pouch Item # 73689 UPC 10083661736898 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1804-2018·2018-08-08

    Sugar Foods Recalls Italian Seasoned Croutons Due to Whey Powder Contamination

    Sugar Foods Corporation is recalling 1 lb. foil pouches of Homestyle Italian Seasoned Croutons because they were made with recalled whey powder.

    Product
    Homestyle Italian Seasoned Croutons: 1 lb. foil pouch Item # 74384 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-1806-2018·2018-08-08

    Sugar Foods Recalls Garlic Butter Focaccia Crumbles Due to Whey Powder Issue

    Sugar Foods Corporation is recalling Garlic Butter and Black Pepper Focaccia Crumbles because they were made with recalled whey powder.

    Product
    Garlic Butter and Black Pepper Focaccia Crumbles: 400 lb. Gaylord Tote Item # 78939 Sugar Foods Corporation 6190 E. Slauson Ave. Los Angeles, CA 90047
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-1023-2018·2018-08-08

    Pfizer Recalls Daptomycin Injection Due to Microbial Contamination

    Pfizer is recalling Daptomycin for Injection due to reports of adverse events indicative of infusion reactions related to microbiological contamination.

    Product
    Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-0106-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2594-2018·2018-08-08

    Integra LifeSciences Recalls Mayfield Infinity XR2 Base Units Due to Fracture Risk

    Integra LifeSciences is recalling Mayfield Infinity XR2 Low Profile Base Units because the knob assembly in the swivel adapter may fracture or break during use.

    Product
    MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp…
    Category
    Medical Device
    Distribution
    Distributed nationwide