The Recall Desk

State

Georgia product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54951–54975 of 83462

  • SevereFDA (Food)·F-1531-2016·2016-06-29

    Candy and Caramel Icing Recalled for Undeclared Milk and Soy Allergens

    The Caramel Factory, LLC. is recalling white and dark chocolate cashew turtles and tortoises, candy, baked goods, and caramel icing due to undeclared milk and soy.

    Product
    white and dark chocolate cashew turtles and tortoises
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·16V482000·2016-06-29

    Ford Recalls 2016 Transit Connects for Brake Pump Contamination

    Ford is recalling 2016 Transit Connect vehicles because metallic debris in the brake pump may degrade electronic stability control, increasing crash risk.

    Product
    FORD — FORD TRANSIT CONNECT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1534-2016·2016-06-29

    Candy and Baked Goods Recalled for Undeclared Milk and Soy Allergens

    The Caramel Factory, LLC. is recalling white and dark chocolate peanut clusters, candy, baked goods, and caramel icing due to undeclared milk and soy.

    Product
    white and dark chocolate peanut clusters
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·16V484000·2016-06-29

    Wabash National Van Trailers Recalled for Spring Brake Valve Defect

    Wabash National is recalling 2015-2017 Van Trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V485000·2016-06-29

    Nissan Recalls 2016 Sentra Vehicles Due to Engine Harness Defect

    Nissan is recalling 1,522 model year 2016 Sentra vehicles because an engine room harness terminal pin may be too large, potentially causing the engine to stall or fail to start.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V481000·2016-06-29

    Newmar Recalls 2017 Motorhomes Due to Wiper and Headlight Defect

    Newmar is recalling 2017 Ventana and Dutch Star motorhomes because wipers may block the view or headlights may turn off, increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA VL, VENTANA, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2047-2016·2016-06-29

    Ceg Enterprises Recalls Germ Terminator Toothbrush Sanitizers Due to Heat and Cord Issues

    Ceg Enterprises is recalling Germ Terminator GT100 toothbrush sanitizers due to reports of excessive heat, power cord discoloration, and suspected counterfeit UL labels.

    Product
    Germ Terminator, Toothbrush Steam Sterilization for Oral Health. Model GT100. The Germ Terminator uses steam heat to sanitize two manual toothbrushes or two toothbrush heads. Water is poured into a reservoir in the device's housing. The steam cycle is followed by a drying…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1556-2016·2016-06-29

    Caramel Factory Caramel Icing Recalled for Undeclared Soy Allergen

    The Caramel Factory is recalling Caramel Icing because it contains undeclared soy, a major food allergen.

    Product
    The Caramel Factory (TM) Caramel Icing, NET WT. 22OZ, 1 LB. 6OZ. (622 grams) and 2.5 GAL bucket
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-2040-2016·2016-06-29

    Immuno-Mycologics Recalls Histoplasma Yeast Complement Fixation Antigen Due to Bacterial Contamination

    Immuno-Mycologics, Inc. is recalling 467 units of Histoplasma Yeast Complement Fixation Antigen Dilute (Lot 111WH3) due to bacterial contamination. The product was distributed nationwide to specific states.

    Product
    Histoplasma Yeast Complement Fixation Antigen Dilute Ref# H30150 The fungal antigens and positive controls are used to detect antibodies in patient serum by the complement fixation (CF) procedure to aid in the diagnosis of four specific fungal diseases: Histoplasmosis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2017-2016·2016-06-29

    Siemens Biograph PET/CT Scanner Upgrade Recalled for Calibration Error

    Siemens Medical Solutions is recalling 2 Biograph TruePoint scanner upgrades because using non-Siemens phantoms for calibration may result in unexpected SUV values.

    Product
    Biograph Sys 16-3R to 16-4R upgrade, MATERIAL NUMBER 10525581 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2044-2016·2016-06-29

    Fresenius CLiC Monitor Recall for Potential Hemodialysis Pump Stoppage

    Fresenius Medical Care is recalling 875 CLiC monitors used with 2008T hemodialysis machines because a frozen screen may cause the blood pump to stop.

    Product
    Crit Line in a Clip (CLiC). CliC P/N: CL 10041001 CLiC is a continuous real-time monitor for non-invasive hematocrit oxygen saturation and percent change in blood volume measurement during hemodialysis treatment. Used in conjunction with the Fresenius 2008T Hemodialysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2005-2016·2016-06-29

    Siemens Biograph mCT-X 4R PET/CT Scanners Recalled for Calibration Error

    Siemens is recalling 83 Biograph mCT-X 4R scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.

    Product
    Biograph mCT-X 4R, MATERIAL NUMBER 10248670 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V480000·2016-06-29

    Kia Recalls 2016 Sorento Vehicles for Rear Suspension Weld Defect

    Kia is recalling 2016 Sorento vehicles because a rear suspension component may not be properly welded, which could break and increase the risk of a crash.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2031-2016·2016-06-29

    Siemens Biograph mCT-S PET/CT Scanners Recalled for Calibration Error

    Siemens Medical Solutions is recalling 100 Biograph mCT-S PET/CT scanners because using non-Siemens phantoms for calibration may result in unexpected SUV values.

    Product
    Biograph mCT-S(40) 4R, MATERIAL NUMBER 10248671 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic information.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2042-2016·2016-06-29

    Surgical Specialties Recalls Sharpoint Polypropylene Suture Due to Contamination

    Surgical Specialties Corporation is recalling Sharpoint Polypropylene Blue Monofilament 9-0 USP suture because it may contain Black Nylon 9-0 suture.

    Product
    Sharpoint Polypropylene Blue Monofilament 6"/15cm 9-0 USP, Product No. J2558N
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-2009-2016·2016-06-29

    Siemens Biograph PET/CT Scanners Recalled for Calibration Error Risk

    Siemens is recalling 46 Biograph 40 TruePoint PET/CT scanners due to a potential for unexpected SUV values if a non-Siemens phantom is used for calibration.

    Product
    BIOGRAPH 40 TruePoint w/TrueV, Material Number 10097304 The Siemens Biograph TruePoint systems are combined X-Ray Computed Tomography (CT) and Positron Emission Tomography (PET) scanners that provide registration and fusion of high resolution physiologic and anatomic…
    Category
    Medical Device
    Distribution
    Distributed nationwide