The Recall Desk

State

Georgia product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40726–40750 of 83441

  • HighFDA (Food)·F-0626-2019·2018-11-28

    Cadence Gourmet Cauliflower & Cheese recall due to potential Salmonella and Listeria contamination

    The FDA is recalling Cadence Gourmet Cauliflower & Cheese because of potential Salmonella and/or Listeria Monocytogenes contamination.

    Product
    Cadence Gourmet Cauliflower & Cheese Net Weight: 10 lbs. (4.4 kg) / cs UPC: 00851124006375 Ingredients: Cauliflower, B¿chamel Sauce (Milk, Cultured Cream, Vegetable Broth [Water, sauteed Vegetables {carrots, celery, onions, tomatoes}, Salt, Yeast Extract, Dried Onion and…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0482-2019·2018-11-28

    GE Healthcare Recalls Panda iRes Infant Radiant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda iRes Infant Radiant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda iRes Infant Radiant Warmer. Device sold under the following product names: Panda iRes Warmer and Panda iRes Bedded Warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0624-2019·2018-11-28

    Cadence Gourmet Roasted Vegetables Recalled for Potential Pathogen Contamination

    Cadence Gourmet LLC is recalling Balsamic Roasted Vegetables due to potential Salmonella and Listeria contamination from McCain Foods USA ingredients.

    Product
    Cadence Gourmet Balsamic Roasted Vegetables; Net Weight: 10 lbs. (4.5 kg)/ cs UPC: 00851124006382 Ingredients: Zucchini, Artichoke, White Balsamic Sauce (Balsamic vinegar {wine vinegar, grape concentrate, Natural Flavor, Contains Sulfites] Olive Oil, Walnut Oil, Honey…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0483-2019·2018-11-28

    GE Healthcare Recalls Panda Freestanding Infant Warmers Due to Electric Leakage

    GE Healthcare is recalling 1,724 Panda Freestanding Infant Warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Panda Freestanding Warmer. Device sold under the following product names: Panda Freestanding Warmer and Panda Freestanding Warmer Generic ATO Model. Infant Radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V844000·2018-11-28

    Porsche Recalls 2017-2018 Models Due to Ski Bag Strap Defect

    Porsche is recalling certain 2017-2018 Cayenne and Macan vehicles because the optional ski bag strap may tear, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE CAYENNE, MACAN, MACAN GTS, MACAN S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0266-2019·2018-11-28

    L. Perrigo Recalls Calcium Carbonate Antacid Tablets Due to Metal Particles

    L. Perrigo is recalling specific lots of calcium carbonate antacid tablets because they were found to contain metal particles.

    Product
    Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-72, Distributed by DZA Brands, LLC, Salisbury, NC 28147, Scarborough, ME 04074], [HealthMart Pharmacy brand NDC: 62011-0295-1, Distributed by McKessen, One…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0481-2019·2018-11-28

    GE Healthcare Recalls Giraffe Infant Warmers Due to Electric Leakage Risk

    GE Healthcare is recalling 1,724 Giraffe infant radiant warmers worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Warmer. Device sold under the following product names: Giraffe Warmer and Giraffe Bedded Warmer. infant radiant warmer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0480-2019·2018-11-28

    GE Healthcare Recalls Giraffe Incubator Carestations Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe Incubator Carestations worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe Incubator Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0486-2019·2018-11-28

    Ascom Telligence Nurse Call System Recalled for Communication Failure

    Ascom (US) Inc. is recalling 57 units of the Telligence Nurse Call System because a gateway defect may prevent device failures from being displayed at staff consoles.

    Product
    Ascom Telligence Nurse Call System
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-0479-2019·2018-11-28

    GE Healthcare Recalls Giraffe OmniBed Neonatal Incubators Due to Electric Leakage

    GE Healthcare is recalling 1,724 Giraffe OmniBed Carestation neonatal incubators worldwide due to a potential electric leakage hazard that could affect users.

    Product
    Giraffe OmniBed Carestation. Neonatal incubator. Device sold under the following product names: Carestation and Carestation CS1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0625-2019·2018-11-28

    Cadence Gourmet Recalls Roasted Vegetable Blend for Potential Pathogen Contamination

    Cadence Gourmet LLC is recalling Roasted Vegetable Blend due to potential Salmonella and Listeria contamination from McCain Foods USA ingredients.

    Product
    Roasted Vegetable Blend; Net Weight: 30 lbs. (12 x 2.5 lb. bags) Corner Bakery Caf¿ Brand Ingredients: Zucchini, artichoke (water, citric acid and calcium chloride). Tomatoes, olive oil, canola oil, garlic, vinegar (potassium metabisulfite), salt, black pepper, spices.…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Food)·F-0654-2019·2018-11-28

    Harvest Food Group Recalls Mexican Style Roasted Corn for Listeria and Salmonella

    Harvest Food Group is recalling Signature Select Mexican Style Roasted Corn due to potential contamination with Listeria monocytogenes or Salmonella.

    Product
    Signature Select Mexican Style Roasted Corn; 12 oz.; 12/12oz. units per case; Keep Frozen Until Ready To Use; UPC 02113094060; Item# 21130-09406
    Category
    Food
    Distribution
    13 states
  • HighFDA (Food)·F-0655-2019·2018-11-28

    Zinetti Roasted Vegetable Blend Recalled for Listeria and Salmonella Risk

    Harvest Food Group is recalling Zinetti Roasted Vegetable Blend due to potential contamination with Listeria monocytogenes or Salmonella.

    Product
    Zinetti Roasted Vegetable Blend; 40lb. bulk case; Keep Frozen; Item# ZIN-RSVB-0040
    Category
    Food
    Distribution
    13 states
  • ModerateFDA (Devices)·Z-0489-2019·2018-11-28

    Merck Minicon Clinical Sample Concentrators Recalled for Performance Issues

    Merck Millipore is recalling Minicon Clinical Sample Concentrators because they may take up to 24 hours to concentrate samples, delaying diagnostic tests.

    Product
    Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon CS-15) Minicon concentrators are non-sterile, disposable, multiwall ultrafiltration devices. Minicon¿ clinical sample concentrators are for in vitro diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0476-2019·2018-11-28

    Ortho-Clinical VITROS dLDL Reagent Recalled for Negatively Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products dLDL Reagent GENs 26 and 27 because the in vitro diagnostic may produce negatively biased results.

    Product
    VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Diagnostic to quantitatively measure LDL Cholesterol (LDLC) Product Code: 6801728 UDI (10758750006793)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0283-2019·2018-11-28

    Dr. Reddy's Recalls Clopidogrel Tablets Due to Dissolution Failure

    Dr. Reddy's Laboratories is recalling specific lots of Clopidogrel Bisulfate tablets because they failed dissolution testing during stability checks.

    Product
    CLOPIDOGREL BISULFATE — CLOPIDOGREL BISULFATE (CLOPIDOGREL BISULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0275-2019·2018-11-28

    Ecolab Recalls Medi-Stat Foam Hand Soap Due to Labeling Error

    Ecolab Inc is recalling 14,108 bottles of Medi-Stat Foam Antimicrobial Hand Soap because the label may not match the formula in the bottle.

    Product
    Medi-Stat Foam, Antimicrobial Hand Soap, Chloroxylenol 0.5%, 1250 mL (42.3 fl oz), OTC, Ecolab, 370 Wabasha Street N, St. Paul, MN 55102, NDC 47593-503-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0388-2019·2018-11-28

    GE Healthcare Recalls DeltaVision OMX SR Imaging Systems Due to Interlock Defect

    GE Healthcare Biosciences is recalling 39 DeltaVision OMX SR Imaging Systems because the safety interlocks are not wired to be single-fault tolerant.

    Product
    DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0667-2019·2018-11-28

    Diamond Crystal Barbecue Sauce Recalled for Missing Ingredient Labels

    Diamond Crystal Brands is recalling House Blend Barbecue Sauce because the labels are missing required ingredient information, including soybean oil.

    Product
    HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calcium Disodium EDTA***DIAMOND CRYSTAL BRANDS, INC. SAVANNAH, GA 31405
    Category
    Food
    Distribution
    11 states
  • ModerateFDA (Drugs)·D-0273-2019·2018-11-28

    Nitrofurantoin Capsules Recalled for Potential Cross-Contamination with Unrelated Ingredients

    American Health Packaging is recalling specific lots of Nitrofurantoin Capsules due to potential cross-contamination with unrelated active ingredients.

    Product
    Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals), 100 mg, 100-count Unit Dose Blisters, Rx only, Amerisource Health Services DBA American Health Packaging, 2550-A John Glenn Avenue Columbus, OH 43217, NDC 68084-446-01 (Individual Dose NDC: 68064-446-11)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0485-2019·2018-11-28

    Tosoh AIA-900 Analyzer Software Issue May Delay Patient Testing

    Tosoh is recalling three AIA-900 immunoassay analyzers due to a software issue that may cause reagent data errors, potentially delaying patient results.

    Product
    Tosoh AIA-900 immunoassay Analyzer
    Category
    Medical Device
    Distribution
    2 states