The Recall Desk

State

Georgia product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42001–42025 of 83441

  • CriticalFDA (Drugs)·D-1202-2018·2018-09-19

    HelloLife Recalls Thyroveev Homeopathic Medicine Due to Microbial Contamination

    HelloLife is recalling 370 bottles of Thyroveev homeopathic medicine due to microbial contamination. The product was distributed nationwide and internationally.

    Product
    Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-025-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3132-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail 130¿ 13 mm x 180 mm, Item Number: 814513180
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3074-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 400 mm, Item Number: 814313400
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3161-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 440 mm, Item Number: 814611440
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3086-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 420 mm, Item Number: 814409420
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3155-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 320 mm, Item Number: 814611320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3048-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Issue

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 300 mm, Item Number 814309300
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3069-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 300 mm, Item Number: 814313300
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3090-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 11 mm x 320 mm, Item Number: 814411320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3087-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 440 mm, Item Number: 814409440
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3070-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 320 mm, Item Number: 814313320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3166-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 320 mm, Item Number: 814613320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3148-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Issue

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 320 mm, Item Number: 814609320
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3107-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 460 mm, Item Number: 814413460
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3129-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 420 mm, Item Number: 814511420
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3068-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 280 mm, Item Number: 814313280
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3054-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 9 mm x 460 mm, Item Number: 814309460
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3134-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 280 mm, Item Number: 814513280
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3135-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 13 mm x 300 mm, Item Number: 814513300
    Category
    Medical Device
    Distribution
    42 states
  • SevereNHTSA·18V647000·2018-09-19

    Spartan Metrostar Emergency Vehicles Recalled for Wheel Stud Defect

    Spartan Motors is recalling 2018-2019 Metrostar emergency vehicles because improperly heat-treated wheel studs may fail, potentially causing the wheel to detach.

    Product
    SPARTAN — SPARTAN METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3082-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 9 mm x 340 mm, Item Number: 814409340
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Devices)·Z-3127-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 11 mm x 380 mm, Item Number: 814511380
    Category
    Medical Device
    Distribution
    42 states
  • SevereNHTSA·18V646000·2018-09-19

    Freightliner Recalls 2018-2019 Models Due to Steering Shaft Defect

    Daimler Trucks North America is recalling 2018-2019 Freightliner 108SD, 114SD, and Business Class M2 vehicles because an incorrectly installed steering shaft may disconnect the steering wheel from the front wheels.

    Product
    FREIGHTLINER — FREIGHTLINER 108SD, 114SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide