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.

Which agencies issued them

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.

36326–36350 of 83373

  • ModerateFDA (Food)·F-2144-2019·2019-09-18

    Calcium Supplement Recalled for Lacking Declared Vitamin D Content

    Jivan Shakti Inc. is recalling 790 bottles of Dr. Naram's Rasayana D Tablet because FDA testing found no Vitamin D in the product.

    Product
    Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement with Vitamin D*, Dietary Supplement, 60 Tablets, FOR EXPORT ONLY, Imported & Distributed by: Jivan Shakti INC, 933 South Street, Peekskill, NY 10566…
    Category
    Food
    Distribution
    20 states
  • LowFDA (Drugs)·D-1848-2019·2019-09-18

    Mylan Recalls Gatifloxacin Ophthalmic Solution Due to Unknown Impurity

    Mylan Pharmaceuticals is recalling Gatifloxacin Ophthalmic Solution 0.5% due to an out-of-specification result for an unknown impurity.

    Product
    Gatifloxacin Ophthalmic Solution 0.5%, 2.5 mL per bottle, Rx Only, Mfd. for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505. Made in India. NDC: 0378-5431-35
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2490-2019·2019-09-18

    Randox Calibration Serum Recalled for Incorrect Analyte Targets

    Randox Laboratories is recalling calibration sera due to realigned targets for AST and ALT. The recall affects 307 kits distributed nationwide and in several foreign locations.

    Product
    This is an in vitro diagnostic product intended for use as a calibration serum in clinical chemistry assays. Randox calibration sera contain 42 analytes and are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1847-2019·2019-09-18

    Lamivudine Tablets Recalled for Incorrect Package Insert Labeling

    American Health Packaging is recalling Lamivudine Tablets due to an error in the package insert that incorrectly lists tablet description coding.

    Product
    Lamivudine Tablets, USP, 150 mg, 30 (3x10) count Unit Dose Blisters Carton, NDC 60687-362-21 (Individual Dose NDC: 60687-362-11), Distributed by American Health Packaging, Columbus, OH
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V656000·2019-09-17

    McNeilus CNG Trucks Recalled for Pressure Relief Device Defect

    McNeilus is recalling 330 CNG-powered trucks from 2013-2018 because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    MCNEILUS — MCNEILUS MA SIDE LOADER, AUTOREACH, STANDARD MIXER, ZERO RADIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V658000·2019-09-17

    Hyundai Translead Recalls 2017-2018 Duralite HT Flatbed Trailers

    Hyundai Translead is recalling 2017-2018 Duralite HT flatbed trailers because bulkhead brackets may break, causing the bulkhead to detach and create a road hazard.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD DURALITE HT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·092-2019·2019-09-17

    Perdue Recalls Frozen Chicken Tenders for Undeclared Wheat Allergen

    Perdue Foods is recalling approximately 495 pounds of frozen chicken breast tenders because they contain undeclared wheat and are mislabeled as gluten-free.

    Product
    Perdue Foods LLC — Perdue Foods LLC Recalls Simply Smart Organics Frozen Chicken Ready-to-Eat Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·19V659000·2019-09-17

    Terex TLM Aerial Vehicles Recalled for Boom Valve Defect

    Terex is recalling 2016-2017 TLM aerial devices because an incorrect holding valve may cause the boom to drift down if a hose bursts.

    Product
    TEREX — TEREX TLM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V655000·2019-09-16

    Airstream Recalls 2016-2017 Trailers Due to Electrical Fire Risk

    Airstream is recalling specific 2016-2017 Flying Cloud and International trailers because an inverter may contact a fuse, creating a fire hazard.

    Product
    AIRSTREAM — AIRSTREAM FLYING CLOUD, INTERNATIONAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V654000·2019-09-12

    Nissan and Infiniti Recall Vehicles for Backup Camera Display Defect

    Nissan is recalling 2018-2019 Nissan and Infiniti vehicles because backup camera settings can be adjusted to hide the rear view image, increasing crash risk.

    Product
    NISSAN — NISSAN, INFINITI ROGUE SPORT, ARMADA, VERSA, ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E062000·2019-09-12

    Chrysler Recalls Mopar Passenger Air Bag Modules Due to Testing Defect

    Chrysler is recalling specific Mopar replacement passenger air bag modules that did not complete developmental testing. These modules may not perform as designed in a crash, increasing injury risk.

    Product
    AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2481-2019·2019-09-11

    OMNIlife ApeX Acetabular Liner Recalled for Oxidation Test Failure

    OMNIlife science Inc. is recalling six ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.

    Product
    OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component ApeX-LNK crosslinked Acetabular Insert, 10 deg hood; Product Code : H5-54840
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2446-2019·2019-09-11

    Stryker Recalls Berchtold Chromophare Monitor Carrier Arms Due to Weld Defects

    Stryker Communications is recalling 52 Berchtold Chromophare Dual Monitor Carrier Arms or Dual Flat Panels because the mounts may have insufficient welds.

    Product
    Berchtold Chromophare Dual Monitor Carrier Arm or Dual Flat Panel, a component of Berchtold Chromophare Ceiling Mounted Surgical Light System.
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-2470-2019·2019-09-11

    B. Braun Epidural Tray Recall Due to Filter Membrane Damage

    B. Braun Medical is recalling 960 epidural trays because filter membrane damage prevents the filter from achieving its intended capacity.

    Product
    CE17TKFCN EPID TRAY W/ 17GA TUOHY NRFIT Catalog # 339186
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2479-2019·2019-09-11

    OMNIlife ApeX Acetabular Liner Recalled for Oxidation Testing Failure

    OMNIlife science Inc. is recalling 14 ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.

    Product
    OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Liner 53-28; Product code: H6-25328
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2474-2019·2019-09-11

    B. Braun Medical Recalls Cont. Epidural Needles Due to Filter Damage

    B. Braun Medical is recalling 1,230 units of CE18TKSTN Cont. Epidural Needles because the filter membrane is damaged, preventing the device from achieving its intended filter capacity.

    Product
    CE18TKSTN CONT EPID W/SOFT TIP NRFIT Catalog # 339191
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2356-2019·2019-09-11

    Norm-O-Temp 111W Medical Device Recalled for Missing Tissue Damage Warning

    Cincinnati Sub-Zero Products LLC is recalling Norm-O-Temp model 111W units because the manual lacks instructions warning that exceeding 40 Celsius for extended periods can cause tissue damage.

    Product
    Norm-O-Temp model 111W
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-2480-2019·2019-09-11

    OMNIlife ApeX Acetabular Liner Recalled for Oxidation Test Failure

    OMNIlife science Inc. is recalling 22 ApeX acetabular liners that failed oxidation testing. The defect may cause higher wear rates, potentially leading to revision surgery.

    Product
    OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28; Product code: H6-25128
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2466-2019·2019-09-11

    B. Braun Medical Recalls Espocan Spinal/Epidural Trial Needles

    B. Braun Medical is recalling 100 units of Espocan Spinal/Epidural Trial Needles because damage to the filter membrane prevents the filter from achieving its intended capacity.

    Product
    ES1725KFXN ESPOCAN SPINAL/EPID TRY NRFIT Catalog # 339114
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Devices)·Z-2468-2019·2019-09-11

    B. Braun Recalls FEF 100N Flat Epidural Filters Due to Membrane Damage

    B. Braun Medical is recalling 250 units of FEF 100N Flat Epidural Filters because damage to the filter membrane prevents the device from achieving its intended filter capacity.

    Product
    FEF 100N FLAT EPIDURAL FILTER NRFIT Catalog # 339160
    Category
    Medical Device
    Distribution
    10 states