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.

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.

49776–49800 of 83452

  • HighUSDA FSIS·pha-042017·2017-04-20

    Conagra Recalls Chicken Nuggets Meal Trays Due to Salmonella Risk

    Conagra Brands is recalling 110,817 pounds of frozen chicken nugget meal trays because the included brownie mix may be contaminated with Salmonella.

    Product
    FSIS Issues Public Health Alert For Chicken Nuggets Meal Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0661-2017·2017-04-19

    Akorn Recalls Latanoprost Ophthalmic Solution Due to Sterility Assurance Issues

    Akorn, Inc. is recalling Latanoprost Ophthalmic Solution, 0.005%, because bottles were found empty, under-filled, or leaking, compromising sterility.

    Product
    LATANOPROST OPHTHALMIC SOLUTION, 0.005%, 125 ug/2.5 mL, packaged in 2.5 mL bottle, Rx only, Manufactured for: Akorn, Inc., Lake Forest, IL 60045, NDC 17478-625-12
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1909-2017·2017-04-19

    SoyNut Butter Company Recalls Blueberry Granola Due to E. coli Risk

    The SoyNut Butter Company is recalling I.M. Healthy Blueberry Granola nationwide due to potential contamination with E. coli O157.

    Product
    I.M. Healthy Blueberry Granola; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1910-2017·2017-04-19

    SoyNut Butter Company Recalls Carb Not Beanit Butter Due to E. coli Risk

    The SoyNut Butter Company is recalling Dixie Diners' Club Carb Not Beanit Butter due to potential E. coli O157 contamination.

    Product
    Dixie Diners' Club Carb Not Beanit Butter, 15oz., Dixie USA, Inc., P.O. Box 1969, Tomball, TX 77377
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1906-2017·2017-04-19

    SoyNut Butter Company Recalls I.M. Healthy Granola Due to E. coli Risk

    The SoyNut Butter Company is recalling I.M. Healthy Original Granola due to potential contamination with E. coli O157.

    Product
    I.M. Healthy, Original Granola; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1911-2017·2017-04-19

    SoyNut Butter Recalled for Potential E. coli O157 Contamination

    The SoyNut Butter Company is recalling B'Gan Quality Product SoyNut Butter due to potential E. coli O157 contamination.

    Product
    B'Gan Quality Product, SoyNut Butter, Creamy; Dist. By: S. Bertram Inc, Linden, NJ 07036
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1903-2017·2017-04-19

    SoyNut Butter Recalled for Potential E. coli O157 Contamination

    The SoyNut Butter Company is recalling I.M. Healthy Unsweetened SoyNut Butter due to potential E. coli O157 contamination. Consumers should stop using the product.

    Product
    I.M. Healthy, Unsweetened SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V260000·2017-04-19

    Tesla Recalls Model S and X for Parking Brake Gear Defect

    Tesla is recalling 2016 Model S and 2016-2017 Model X vehicles because a parking brake gear may fracture, potentially causing the vehicle to roll or become immobile.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1777-2017·2017-04-19

    Welch Allyn ProBP 2400 Digital Blood Pressure Device Recall

    Welch Allyn is recalling 981 ProBP 2400 digital blood pressure devices due to a defective electrical component that may cause over-voltage battery charging and melting of plastic parts.

    Product
    Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ONLY, Made in China --- Distributed by Welch Allyn Inc., 4341 State Street Road, Skaneateles Falls, NY 13153 --- Microlife Corporation 9F, 431, RuiGuang Road, NeiHu, Taipei, 11492, Taiwan, R.O.C.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1908-2017·2017-04-19

    I.M. Healthy Apple Granola Recalled for Potential E. coli O157 Contamination

    The SoyNut Butter Company is recalling I.M. Healthy Apple Granola due to potential E. coli O157 contamination. The product was distributed nationwide.

    Product
    I.M. Healthy Apple Granola; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1761-2017·2017-04-19

    PerkinElmer Recalls Specimen Gate Laboratory Software Due to Data Errors

    PerkinElmer is recalling 29 units of Specimen Gate Laboratory software due to a potential for errors in patient results. The software is used for processing laboratory data.

    Product
    Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing software used in the storage, retrieving, and processing of laboratory data.
    Category
    Medical Device
    Distribution
    23 states
  • SevereNHTSA·17V263000·2017-04-19

    Gillig Recalls 2015-2016 Low Floor Buses for Suspension Defect

    Gillig is recalling 2,604 Low Floor transit buses because improperly seated snap rings in the suspension kneeling modules may cause a loss of air pressure, increasing crash risk.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1904-2017·2017-04-19

    SoyNut Butter Recalled for Potential E. coli O157 Contamination

    The SoyNut Butter Company is recalling I.M. Healthy Honey Creamy SoyNut Butter due to potential E. coli O157 contamination.

    Product
    I.M. Healthy, Honey Creamy SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1905-2017·2017-04-19

    SoyNut Butter Recalled for Potential E. coli O157 Contamination

    The SoyNut Butter Company is recalling I.M. Healthy Chocolate SoyNut Butter due to potential E. coli O157 contamination.

    Product
    I.M. Healthy, Chocolate SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1902-2017·2017-04-19

    SoyNut Butter Recalled for Potential E. coli O157 Contamination

    The SoyNut Butter Company is recalling I.M. Healthy Chunky SoyNut Butter due to potential E. coli O157 contamination. The product was distributed nationwide.

    Product
    I.M. Healthy, Chunky SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1773-2017·2017-04-19

    Draegar Delta XL Patient Monitors Recalled for Low Oxygen Alarm Failure

    Draegar Medical Systems is recalling Delta XL patient monitors because the low oxygen alarm may fail to sound when oxygen levels drop below the limit.

    Product
    Delta XL, Catalog Number: MS18596 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Product Usage: The devices are intended to be used in the environment where patient care is provided by Healthcare Professionals, i.e. Physicians…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0664-2017·2017-04-19

    Medisca Recalls Estrone USP Bulk Due to cGMP Deviations

    Medisca, Inc. is recalling Estrone, USP Bulk in various bottle sizes due to current Good Manufacturing Practice (cGMP) deviations identified during an FDA inspection.

    Product
    ESTRONE, USP Bulk, in a) 100 mgs (NDC 38779-0891-05), b) 1 gram (NDC 38779-0891-06), c) 5 grams (NDC 38779-0891-03), d) 25 grams (NDC 38779-0891-04), and e) 100 grams (NDC 38779-0891-09) Bottles, Packed by MEDISCA INC. PLATTSBURGH, NY 12901; Product Code 0891
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1907-2017·2017-04-19

    SoyNut Butter Company Recalls Granola Due to E. coli O157 Risk

    The SoyNut Butter Company is recalling I.M. Healthy Raisin & Cranberry Granola due to potential E. coli O157 contamination.

    Product
    I.M. Healthy Raisin & Cranberry Granola; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1901-2017·2017-04-19

    SoyNut Butter Recalled for Potential E. coli O157 Contamination

    The SoyNut Butter Company is recalling I.M. Healthy Creamy SoyNut Butter nationwide due to potential E. coli O157 contamination.

    Product
    I.M. Healthy, Creamy SoyNut Butter; Peanut Free; The SoyNut butter Company, Glenview, IL 60025
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1757-2017·2017-04-19

    ConMed Recalls Hyfrecator 2000 ESU Cartons with Non-Sterile Handpiece Sheaths

    ConMed is recalling Hyfrecator 2000 ESU cartons because they were packaged with non-sterile handpiece sheaths labeled as sterile, posing a risk of infection.

    Product
    Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 115 VOLTS AC, REF/Catalog Number 7-900-115, Rx Only . There is no problem with the Hyfrecator 2000 Electrosurgical Units.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1785-2017·2017-04-19

    Windstone Medical Recalls Cataract Packs Due to Sterile Packaging Concerns

    Windstone Medical Packaging is recalling 7,508 cataract packs because the sterile packaging of the included eye pads may be compromised.

    Product
    Cataract Pack, part numbers 008886-1, AMS2806, PSS3442, PSS3442(A, WAL1155, and WAL1155(A. Product packaged in a convenient manner for use in a general clinical procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1760-2017·2017-04-19

    ConMed Recalls Hyfrecator 2000 Handpiece Sheaths Due to Sterility Labeling Error

    ConMed is recalling Hyfrecator 2000 handpiece sheaths because non-sterile units were packaged in pouches labeled as sterile, posing a risk of infection.

    Product
    HYFRECATOR 2000 HANDPIECE SHEATH, REF/Part Number 7-796-19, Rx ONLY, STERILE, Single Patient Use -- CONMED CORPORATION, 525 FRENCH ROAD UTICA, NY 13502. --- There is no problem with the Hyfrecator 2000 Electrosurgical Units or with cases of P/N 7-796-19 sold in cases as P/N…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1798-2017·2017-04-19

    Windstone Medical Setup Packs Recalled for Potential Sterility Compromise

    Windstone Medical Packaging is recalling 500 Setup Packs containing Medtronic Curity Eye Pads due to potential sterile packaging compromise.

    Product
    Setup Pack, part number AMS3112(A Product packaged in a convenient manner for use in a general clinical procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1793-2017·2017-04-19

    Windstone Medical Minor Operation Kit Recall Due to Sterile Packaging Concerns

    Windstone Medical Packaging is recalling 700 Minor Operation Kits because the sterile packaging of the included Medtronic Curity Eye Pad may be compromised.

    Product
    Minor Operation Kit, part number AMS1530 Product packaged in a convenient manner for use in a general clinical procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide