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.

43701–43725 of 83444

  • ModerateFDA (Devices)·Z-1900-2018·2018-05-30

    Madison Polymeric Engineering Recalls Draco Enzymatic Deep-Cleaning Pads

    Madison Polymeric Engineering is recalling Draco Enzymatic Deep-Cleaning Pads due to microbial contamination with Yarrowia lipolytica, which causes an unpleasant odor.

    Product
    Draco Enzymatic Deep-Cleaning Pad, Draco Pad infused with Simple2 Enzymatic Detergent, Catologue Number HY0305Z
    Category
    Medical Device
    Distribution
    40 states
  • ModerateFDA (Drugs)·D-0837-2018·2018-05-30

    Lupin Recalls My Way Emergency Contraception Tablets for Lack of Approval

    Lupin Pharmaceuticals is recalling My Way emergency contraception tablets because the 2-pack configuration was marketed without the required regulatory approval.

    Product
    My Way (Levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, GAVIS Pharmaceuticals, A Lupin Group Company; Mfg. for Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, UPC 3 43386-622-31 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1912-2018·2018-05-30

    Spinal Elements Recalls Omega Lumbar Interbody Fusion Devices

    Spinal Elements is recalling 19 Omega Lumbar Interbody Fusion Devices because they were assembled with components that do not match the labeled lordosis angle.

    Product
    AMENDIA Omega Lumbar Interbody Fusion Device, Part Number 72-00-2-092812-11 The OmegaLIF(TM) (LIF(TM)) Expandable Lumbar Interbody Device is designed for use in intervertebral body spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) at…
    Category
    Medical Device
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1899-2018·2018-05-30

    Madison Polymeric Engineering Recalls Flexible Endoscope Pre-Clean Kits

    Madison Polymeric Engineering is recalling First Step EP-4 Flexible Endoscope Bedside Pre-Clean Kits due to microbial contamination with Yarrowia lipolytica.

    Product
    Travel Kit, First Step EP-4 Kit (200 mL) and 1 Soiled Scope Bag (White), Flexible Endoscope Bedside Pre-Clean Kit, Catalogue Number TK-200(W)
    Category
    Medical Device
    Distribution
    40 states
  • ModerateFDA (Drugs)·D-0838-2018·2018-05-30

    Lupin Recalls My Way Levonorgestrel Tablets for Lack of Approved NDA

    Lupin Pharmaceuticals is recalling My Way (levonorgestrel) emergency contraception tablets because the 2-pack configuration was marketed without an approved New Drug Application.

    Product
    My Way (levonorgestrel) Tablets TWO PACK, 1.5 mg each, packaged as 2 Treatments (Two 1.5mg Levonorgestrel Tablets) per carton, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202; Manufactured by: Lupin Limited, Pithampur (M.P.) - 454 775, INDIA, UPC 3 68180…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1920-2018·2018-05-30

    Implant Direct Legacy 4 Implant Recalled for Mislabeling

    Implant Direct Sybron Manufacturing is recalling 18 units of Legacy 4 Implants due to a mislabeled vial cap. The main label was correct, but the cap showed the wrong part number.

    Product
    ImplantDirect Legacy 4 Implant, 5.7mmD x 5.7mmD Platform, Part 885708, Rx, Sterile. The incorrect cap label shows part 855708, 5.7mmD Platform, 8mmL.
    Category
    Medical Device
    Distribution
    10 states
  • SevereNHTSA·18V351000·2018-05-29

    Western Star 4900 Trucks Recalled for Brake Hose Chafing Risk

    Daimler Trucks North America is recalling 2012-2019 Western Star 4900 trucks because front brake hoses may chafe against the hood, potentially reducing braking effectiveness.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V353000·2018-05-29

    Daimler Trucks Recalls 2017-2019 Models for Brake Caliper Bolt Issue

    Daimler Trucks North America is recalling 8,741 trucks because brake caliper mounting bolts may be insufficiently tightened, potentially reducing braking performance and increasing crash risk.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER, FCCC 5700, 4900, 4700, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V352000·2018-05-29

    Thomas Built Buses Recalling School Buses for Brake Bolt Issue

    Daimler Trucks North America is recalling 2,767 Thomas Built Buses Saf-T-Liner models from 2017-2019 because brake caliper mounting bolts may be insufficiently tightened.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER C2, SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V348000·2018-05-29

    Altec Recalls Aerial Devices Missing Towing Limit Placards

    Altec is recalling 2012-2018 aerial devices missing a placard stating maximum towing limits, which could lead to an overloaded receiver tube and increased crash risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V342000·2018-05-27

    GM Recalls 2018 Chevrolet Sonic for Driver Seat-Back Welding Defect

    General Motors is recalling 2018 Chevrolet Sonic vehicles because a joint in the driver's seat-back frame may not be properly welded, which could reduce strength in a crash.

    Product
    CHEVROLET — CHEVROLET SONIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V344000·2018-05-25

    Chrysler Recalls 2019 Jeep Cherokee for Engine Component Defects

    Chrysler is recalling 2019 Jeep Cherokee vehicles with 2.0L engines due to missing valve stem keepers or reversed camshaft caps that may cause engine failure and stalling.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V343000·2018-05-25

    2018 Jeep Wrangler Recall for Steering Shaft Weld Defect

    Chrysler is recalling 2018 Jeep Wrangler vehicles because a steering shaft weld may split, potentially causing loss of steering responsiveness and increasing crash risk.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V347000·2018-05-25

    Maserati Recalls 2018 Models Due to Front Sub Frame Weld Defects

    Maserati is recalling 2018 Levante, Ghibli, and Quattroporte vehicles because incomplete front sub frame welds may break, potentially causing loss of vehicle control.

    Product
    MASERATI — MASERATI LEVANTE, GHIBLI, QUATTROPORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V340000·2018-05-24

    GMC Recalls 2018 Terrain Models Due to Air Bag Module Software Defect

    General Motors is recalling 2018 GMC Terrain vehicles because the air bag control module may fail to power down, potentially preventing air bag deployment in a crash.

    Product
    GMC — GMC TERRAIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18166·2018-05-24

    IKEA Recalls SLADDA Bicycles Due to Belt Breakage and Fall Hazard

    IKEA is recalling approximately 4,900 SLADDA bicycles sold in the U.S. because the belt can break, posing a fall hazard. No injuries have been reported in the U.S.

    Product
    SLADDA bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18164·2018-05-24

    Bluefin Recalls Wireless Phone Chargers Due to Burn Hazard

    Bluefin International is recalling about 3,000 wireless phone chargers because they can overheat and cause burns. Consumers should stop using them and contact the company for a refund.

    Product
    Wireless phone chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide