The Recall Desk

State

Georgia product recalls

72,940 recalls have nationwide distribution and so reach Georgia. 9,588 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,588
Critical
1,464
Severe
2,164
Most recent
2026-09-09

Of the 9,588 recalls naming Georgia we have scored against our rubric, 1,464 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,164 (23%) are Severe.

These figures cover only the 9,588 recalls whose distribution notice names Georgia specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3851–3875 of 82528

  • HighCPSC·26194·2026-01-15

    HEZI power strips recalled over an ungrounded metal enclosure

    About 1,320 HEZI brand power strips are being recalled because they have an ungrounded metal enclosure that poses an electrocution hazard if energized.

    Product
    HEZI Branded Power Strips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26183·2026-01-15

    Energizer lanterns recalled because the lithium-ion battery can overheat

    About 4,100 Energizer Large Power Indicator Lanterns are being recalled because the lithium-ion batteries installed in them can overheat, posing a burn hazard.

    Product
    Energizer® Large Power Indicator Lanterns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0410-2026·2026-01-14

    Chanachur snack recalled over undeclared peanuts in 95 boxes

    South Asian Food is recalling 95 boxes of Bengal King Jhal Chanachur food treats because the product contains undeclared peanuts. The FDA has classified the action as Class I.

    Product
    Bengal King Jhal Chanachur food treats 12.34oz (350gm)
    Category
    Food
    Distribution
    10 states
  • CriticalFDA (Food)·H-0374-2026·2026-01-14

    Locatelli pecorino romano shippers recalled after testing positive for Listeria

    Ambriola is recalling 184 units of Locatelli Grated Pecorino Romano 48/8oz shippers after the product tested positive for Listeria monocytogenes.

    Product
    Locatelli Grated Pecorino Romano 48/8oz Shipper, Plastic Cup & Lid, 48 units per case
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Food)·H-0372-2026·2026-01-14

    Boar's Head pecorino romano in five pound bags recalled over Listeria

    Ambriola is recalling 405 five-pound bags of Boar's Head Pecorino Romano Grated after the product tested positive for Listeria monocytogenes.

    Product
    Boar's Head Pecorino Romano Grated, 5-pound plastic bag (unit)
    Category
    Food
    Distribution
    20 states
  • CriticalFDA (Devices)·Z-1002-2026·2026-01-14

    Mini Plus surgical kits recalled as not suitable for organ transplant

    AVID Medical is recalling 380 Halyard Mini Plus Kit South units because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard MINI PLUS KIT SOUTH, Kit Code: JACK097-08
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0288-2026·2026-01-14

    ReBoost nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ReBoost Nasal Spray after the products were found to contain yeast, mold and microbial contamination identified as Achromobacter.

    Product
    REBOOST — REBOOST (SILVER NITRATE,EUPHORBIA RESINIFERA RESIN, CALCIUM SULFIDE, GOLDENSEAL, POTASSIUM DICHROMATE,LUFFA OPERCULATA FRUIT, SODIUM CARBONATE, ECHINACEA UNSPECIFIED, CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE AND PULSATILLA VULGARIS)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1000-2026·2026-01-14

    Organ recovery packs recalled as not suitable for organ transplant

    AVID Medical is recalling 132 Halyard Organ Recovery OR Packs, kit code LLOG1000-15, because the devices are not suitable for organ transplant.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOG1000-15.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1001-2026·2026-01-14

    Organ recovery surgical packs recalled as not suitable for organ transplant

    AVID Medical is recalling 52 Halyard Organ Recovery OR Packs because the devices are not suitable for organ transplant. The FDA has classified the action as Class I.

    Product
    Halyard ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0289-2026·2026-01-14

    ClearLife allergy nasal spray recalled over yeast, mold and microbial contamination

    MediNatura is recalling all lots within expiry of ClearLife Allergy Nasal Spray, Extra Strength, after the products were found to contain yeast, mold and Achromobacter.

    Product
    CLEARLIFE EXTRA STRENGTH — CLEARLIFE EXTRA STRENGTH (ONION, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, LUFFA OPERCULATA FRUIT, SULFUR, AMBROSIA ARTEMISIIFOLIA WHOLE, EUPHRASIA STRICTA AND SCHOENOCAULON OFFICINALE SEED)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0373-2026·2026-01-14

    Ambriola Piccante pecorino romano recalled after testing positive for Listeria

    Ambriola is recalling 179 bags of Ambriola Piccante grated Pecorino Romano in 5 and 10-pound sizes after the product tested positive for Listeria monocytogenes.

    Product
    Ambriola Piccante grated Pecorino Romano, 5 and 10-pound plastic bags (units)
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1034-2026·2026-01-14

    Head fixation devices recalled because a torque screw may crack or separate

    IMRIS Imaging is recalling 122 HFD100 Head Fixation Devices because a torque screw may crack or separate, which could lead to inadequate head stabilization and risk of patient injury.

    Product
    Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog Number: 119695-000, 119629-000, 119630-000, 113803-000, 113803-600, 113802-000, 113802-600 Software Version: Not Applicable Product Description: The HFD100 Head Fixation Device provides rigid skeletal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1032-2026·2026-01-14

    Emergency call stations recalled over missing low battery alerts

    Securitas Healthcare is recalling 1,898 Arial 900 MHz Call Stations, model CSK200-900MR, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.

    Product
    Arial 900 MHz Call Station, Model Number CSK200-900MR, with Firmware version: 1.6.3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0392-2026·2026-01-14

    Italian parsley recalled over the pathogen Cyclospora cayetanensis

    MAYEJ Comercializadora is recalling 1,288 boxes of Italian Parsley over the pathogen Cyclospora cayetanensis.

    Product
    Italian Parsley packaged in 24lb boxes, 40 bunches per box in plastic.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1028-2026·2026-01-14

    Medication dispensing servers recalled over delayed updates from enterprise systems

    CareFusion 303 is recalling 2,079 BD Pyxis ES Enterprise Server systems over a software issue that may result in equipment not receiving timely updates of patient or medication information.

    Product
    BD Pyxis ES Enterprise Server Catalog Numbers 1115-00, 137672-02,137672-03 137671-02, 137671-03, 137670-02, 137670-03, 139676-01, 139421-01, 139420-01, 139419-01, 139419-02, 139673-01, 137081-01, 136451-01, 136451-02, 136450-01, 136450-02, 136449-01, 136449-02, 134148-01, 133760
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0351-2026·2026-01-14

    Aluminum sauce pans recalled after testing found leachable lead levels

    Town Food Service Equipment is recalling approximately 11,300 aluminum sauce pans in 1QT to 3QT sizes after the product was found to contain leachable lead levels.

    Product
    Town Food Service EQ CO Inc. brand Aluminum Sauce Pans in 1QT, 1.5QT, 2 QT, and 3QT sizes; UPC Codes: 843784003559, 843784003566, 843784003573, 843784003580
    Category
    Consumer Product
    Distribution
    35 states
  • HighFDA (Devices)·Z-1027-2026·2026-01-14

    Patient monitors recalled over unvalidated intracranial and bladder pressure measurements

    Remote Diagnostic Technologies is recalling 7,129 Philips Tempus Pro Patient Monitors because intracranial and bladder pressure measurements have not been tested or validated for accuracy.

    Product
    Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R. USB 2-Channel IBP Module, REF: 01-2017. Used with User/Operator Manual
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1031-2026·2026-01-14

    Arial call stations recalled over a firmware issue affecting battery alerts

    Securitas Healthcare is recalling 5,627 Arial 900 MHz Call Stations, model CSK200-900, because a firmware issue may prevent a low battery alert being transmitted before the battery fails.

    Product
    Arial 900 MHz Call Station, Model Number CSK200-900, with Firmware version: 1.6.3
    Category
    Medical Device
    Distribution
    Distributed nationwide