The Recall Desk

State

Georgia product recalls

73,817 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.

Which agencies issued them

These figures cover only the 9,635 recalls whose distribution notice names Georgia specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48276–48300 of 83452

  • HighFDA (Devices)·Z-2692-2017·2017-07-19

    St. Jude Medical Recalls Proclaim 7 Elite Implantable Pulse Generators

    St. Jude Medical is recalling 9,529 Proclaim 7 Elite implantable pulse generators due to a risk of losing neuromodulation therapy when exposed to monopolar electrosurgical devices.

    Product
    Proclaim 7 Elite, Implantable Pulse Generator, REF 3662, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2712-2017·2017-07-19

    Toshiba APLIO i-series Ultrasound Systems Recalled for Incorrect Velocity Readings

    Toshiba is recalling 28 APLIO i-series diagnostic ultrasound systems because they may display incorrect velocity values when using the Continuous Trace method.

    Product
    APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 TUS AI800 diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2714-2017·2017-07-19

    ArjoHuntleigh Flowtron ACS900 Medical Pump Recalled for Deflation Failure

    Arjo, Inc. is recalling 40,675 Flowtron ACS900 medical pumps worldwide because the device may fail to deflate the calf garment as intended without triggering an alarm.

    Product
    ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2698-2017·2017-07-19

    Arrow Recalls EVOLUTION Pressure Injectable PICC Catheters Due to Hub Tab Detachment

    Arrow International is recalling EVOLUTION Pressure Injectable PICC catheters because the peel-away component hub tabs may prematurely detach during use.

    Product
    Arrow EVOLUTION Pressure Injectable PICC with Chlorag+ard Antimicrobial and Antithrombogenic Technology
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-2550-2017·2017-07-19

    Matlaws Pre-Cooked Fish Sticks Recalled for Undeclared Milk

    National Fish & Seafood, Inc. is recalling Matlaws All Natural Panko Pre-Cooked Fish Sticks because the product may contain undeclared milk.

    Product
    MATLAWS ALL NATURAL PANKO PRE COOKED FISH STICKS 1/10 LB and 10/2 LB
    Category
    Food
    Distribution
    24 states
  • HighFDA (Devices)·Z-2727-2017·2017-07-19

    Natus Neurology Recalls Elite Obstetric Probes Due to Excessive Background Noise

    Natus Neurology is recalling 2,335 Elite Obstetric probes because excessive background noise may mask fetal heart rate and blood flow monitoring.

    Product
    Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe, Model #: X1L008, Catalog Code: NW20. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.
    Category
    Medical Device
    Distribution
    44 states
  • HighFDA (Food)·F-2588-2017·2017-07-19

    NatureBox Mini Crispy Snickerdoodles Recalled for Cashew Fragment

    NatureBox is recalling Mini Crispy Snickerdoodles because a cashew fragment was found during packing, posing a potential allergen risk.

    Product
    NatureBox Mini Crispy Snickerdoodles: Cinnamon-sugar cookies made with whole wheat. Contains: Wheat, Milk and Egg.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2463-2017·2017-07-19

    3CS Organics Recalls HIPP Infant Formula Due to Labeling Issues

    3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack full English labeling.

    Product
    HIPP HA Combiotik HA 1, 500g (4/case), HIPP Combiotik HA 2, 500g (4/case), HA Combiotik Pre HA, 500g (4/case), HIPP Combiotic Growing Up Milk 3, 600g (4bx/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2711-2017·2017-07-19

    Toshiba APLIO 500 Ultrasound Systems Recalled for Incorrect Velocity Trace Values

    Toshiba American Medical Systems Inc. is recalling 307 APLIO 500 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method on Spectral Doppler.

    Product
    APLIO 500 TUS-A500 diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2380-2017·2017-07-19

    Source Naturals Hydrogen Boost Capsules Recalled for Undeclared Boron

    Source Naturals Hydrogen Boost Capsules are being recalled because they contain low levels of undeclared boron. The recall covers 55,354 units distributed nationwide.

    Product
    Source Naturals Hydrogen Boost Capsule: 6 Count Trial, 30 Count, 60 Count; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1855: 60 count Bottle - Product SN1856; 6 count Bottle - Product SN2314; 30 count + 30…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2464-2017·2017-07-19

    3CS Organics Recalls HIPP Organic Infant Milk Products for Labeling Issues

    3CS Organics is recalling HIPP Organic infant milk products because they are not FDA approved and lack full English labeling.

    Product
    HIPP Organic Comb Hungry Infant Milk, 800g (4bx/case), HIPP Organic Comb First Infant Milk, 800g (4bx/case), HIPP Organic Combiotic Follow on Milk 2, 800g (4bx/case), HIPP Organic Good Night Milk from 6 Months, 350g (12cans/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2584-2017·2017-07-19

    Lyrical Foods Recalls Kite Hill Almond Yogurt Due to Spoilage

    Lyrical Foods is voluntarily recalling Kite Hill Almond Yogurt because some packages spoiled before the best by date.

    Product
    Kite Hill Almond Yogurt, Strawberry ,NET WT. 5.3 oz (150G) ; Case UPC: 8-56624-00414-2 Distributed by Lyrical Foods, Hayward, CA.
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-2465-2017·2017-07-19

    HIPP Infant Formula Recalled for Lack of FDA Approval and English Labels

    3CS Organics LLC is recalling HIPP infant formula products because they are not FDA approved and lack complete English labeling.

    Product
    HIPP Tetrapack-Liquid , Single Serve Combiotik Hungry Infant, 200mL (6pk/24cases), HIPP Tetrapak-Liquid, Single Serve Combiotik First Infant Milk, 200mL (6pk/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2708-2017·2017-07-19

    Toshiba XARIO 100 Ultrasound Systems Recalled for Incorrect Velocity Readings

    Toshiba American Medical Systems is recalling seven XARIO 100 diagnostic ultrasound systems because they may display incorrect values when using the Continuous Trace method for velocity measurements.

    Product
    XARIO 100 TUS-X100 diagnostic ultrasound system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2469-2017·2017-07-19

    3CS Organics Recalls Topfer Lactana Bio Infant Formula for Labeling Issues

    3CS Organics LLC is recalling Topfer Lactana Bio infant and follow-up formula because the product is not FDA approved and lacks complete English labeling.

    Product
    Topfer Lactana Bio 1 Anfangsmilch, 600g (3/case), Topfer Lactana Bio 2, Bio Folgemilch, 600g (3bx/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2462-2017·2017-07-19

    3CS Organics Recalls HIPP Bio Combiotik Infant Formula for Labeling Issues

    3CS Organics LLC is recalling HIPP Bio Combiotik infant formula products because they are not FDA approved and not all products are labeled in English.

    Product
    HIPP Bio Combiotik 1, Canister, 900g (4/case), HIPP Bio Combiotik 2, Canister, 900g (4/case), HIPP Bio Combiotik 3, Canister, 900g (4/case), HIPP Bio Combiotik 1, 600g (4bx/case), HIPP Bio Combiotik 2, 600g (4bx/case), HIPP Bio Combiotik 3, 600g (4/case), HIPP Bio Compiotik…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2467-2017·2017-07-19

    HOLLE Organic Infant Formula Recalled for Lack of FDA Approval

    3CS Organics LLC is recalling HOLLE organic infant formula products because they are not FDA approved and lack English labeling.

    Product
    HOLLE Bio Zulgelingen Opvolgmelk 2, (3/case), HOLLE Bio Lait de suite, 2, 400g (6/case), HOLLE Bio Lait pour Nourrissons Zulgelingenmelk, 400g (6/case), HOLLE Lait Pour Nourrissons 1er Age Bio, 400g (6/case). HOLLE Bio Lait de Suit Au Lait De Chevre, 400g (6/case) , HOLLE…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2582-2017·2017-07-19

    Lyrical Foods Recalls Kite Hill Almond Yogurt Due to Spoilage

    Lyrical Foods is voluntarily recalling Kite Hill Almond Yogurt because some packages spoiled before the best by date.

    Product
    Kite Hill Almond Yogurt, Pineapple, NET WT. 5.3 oz (150G) Case UPC: 8-56624-00435-7 Distributed by Lyrical Foods, Hayward, CA.
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Devices)·Z-2730-2017·2017-07-19

    Beckman Coulter Synchron AQUA CAL Level 1 Calibration Kits Recalled

    Beckman Coulter is recalling Synchron AQUA CAL Level 1 kits due to a sodium recovery shift that may affect system calibration.

    Product
    Beckman Coulter Synchron AQUA CAL Level 1, Part No. 471288 Product Usage: Used for the system calibration of Na, K, Cl, Urea N, Urea, Glucose Creatine, Ca, CO2, and P in UniCel DxC Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2383-2017·2017-07-19

    Source Naturals Renewal Antioxidant Tablets Recalled for Undeclared Boron

    Threshold Enterprises Ltd is recalling Source Naturals Renewal Antioxidant Tablets because they contain low levels of undeclared boron.

    Product
    Source Naturals Renewal Antioxidant Tablet: 10 Count Sample Pack, 30 Count, 60 Count, & 120 Count per bottle; Ingredient: Maltodextrin, Cellulose (Capsules, Silica and magnesium stearate; 30 count Bottle - Product SN1750: 60 count Bottle - Product SN1751; 120 count…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2581-2017·2017-07-19

    Lyrical Foods Recalls Kite Hill Almond Yogurt Due to Spoilage

    Lyrical Foods is voluntarily recalling Kite Hill Almond Yogurt because some packages spoiled before the best by date.

    Product
    Kite Hill Almond Yogurt, Peach, NET WT. 5.3 oz (150G) Case UPC: 8-56624-00415-9 Distributed by Lyrical Foods, Hayward, CA.
    Category
    Food
    Distribution
    15 states
  • ModerateFDA (Food)·F-2461-2017·2017-07-19

    HIPP Anti-Reflux Infant Formula Recalled for Lack of FDA Approval

    3CS ORGANICS LLC is recalling HIPP Anti-Reflux AR Bio-Spezialnahrung because the product is not FDA approved and lacks complete English labeling.

    Product
    HIPP Anti-Reflux AR Bio-Spezialnahrung, 500g (4/case)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2715-2017·2017-07-19

    CryoLife On-X Prosthetic Heart Valve Recall for Incorrect Labeling

    CryoLife, Inc. is recalling 52 On-X Prosthetic Heart Valves because the sewing ring type was mislabeled as Standard instead of Anatomic.

    Product
    On-X Prosthetic Heart Valve Product Usage: Indicated for the replacement of diseased, damaged, or malfunctioning native or prosthetic heart valves in the aortic and mitral positions
    Category
    Medical Device
    Distribution
    Distributed nationwide