The Recall Desk

State

Georgia product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57151–57175 of 83468

  • HighFDA (Devices)·Z-0766-2016·2016-02-17

    Philips TraumaDiagnost X-ray Units Recalled for Arm Fall Hazard

    Philips is recalling TraumaDiagnost radiological examination units because the arm may not be fastened securely and could fall down.

    Product
    Philips Healthcare TraumaDiagnost; Codes: 72001, 720011, 720013, 720020; A radiological examination unit for emergency work and routine skeletal diagnosis.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-0549-2016·2016-02-17

    Zingerman's Candy Bars Recalled for Undeclared Soy and Milk Allergens

    Zingerman's Candy Manufactory is recalling Zzang! Holiday 4 pack Candy Bars due to undeclared soy and milk allergens.

    Product
    Zzang! Holiday 4 pack Candy Bars, 10.5 oz., packaged in preprinted cardboard boxes
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-0688-2016·2016-02-17

    Moog Recalls Curlin Infusion Pumps Due to Calibration Defect

    Moog is recalling specific Curlin infusion pumps because calibration errors may cause them to deliver medication faster than programmed.

    Product
    Moog Curlin Infusion, Ambulatory Infusion Pump The Curlin Ambulatory Infusion System includes Curlin Ambulatory multi-therapy and PainSmart pumps. Curlin 4000, catalog number 340; Curlin 6000, 6000 CMS, and PainSmart IOD, catalog number 360; and Curlin Pump Calibration Set…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0787-2016·2016-02-17

    DePuy SIGMA HP MBT Non-Keel Punch Knee Instrument Recalled

    DePuy Orthopaedics is recalling 351 SIGMA HP MBT Non-Keel Punch Knee Instruments due to a design defect that may cause surgical complications.

    Product
    SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be used as an option in stabilizing the tibial trial during trial reduction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V090000·2016-02-17

    Navistar Recalls 2016 IC CE Buses for Hood Strap Defect

    Navistar is recalling 104 model year 2016 IC CE commercial buses because hood straps may elongate, causing the hood to open unexpectedly during braking and obstructing the driver's vision.

    Product
    IC BUS — IC BUS CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0565-2016·2016-02-17

    Celestial Seasonings Roastaroma Herbal Tea Recalled for Gluten Mislabeling

    Hain Celestial is recalling Roastaroma Herbal Tea because some packages are labeled 'Gluten Free' but contain barley.

    Product
    Celestial Seasonings Roastaroma Herbal Tea Lot code: Best Before 20DEC17 Pack size: 6 retail units (20 count)/ per case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0550-2016·2016-02-17

    Zingerman's Recalls Chocolate Marshmallows Due to Undeclared Soy

    Zingerman's Candy Manufactory is recalling 8-ounce bags of Chocolate Marshmallows because they contain undeclared soy. The recall affects 134 units distributed across 18 states and Washington, D.C.

    Product
    Chocolate Marshmallows, 8 oz., packaged in plastic bags, UPC 8 44397 00077 5
    Category
    Food
    Distribution
    18 states
  • HighCPSC·16103·2016-02-17

    Michaels Recalls Artificial Poinsettias Due to Mold Exposure Risk

    Michaels is recalling Ashland artificial poinsettia stems and bushes because mold may be present, posing a risk of respiratory or other infections.

    Product
    Ashland Poinsettia Stems and Bushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0788-2016·2016-02-17

    Zimmer Biomet Recalls Endobon Xenograft Granules Due to Cytotoxicity Failure

    Biomet France SARL is recalling Endobon-Xenograft Granules because the product failed cytotoxicity tests at 36 months. Use past the 18-month shelf life may cause patient illness or injury.

    Product
    Endobon-Xenograft Granules, Zimmer Biomet, Synthetic Bone Grafting Material, used in dental and/or surgical procedures. Endobon Xenograft Granules, Bone Grafting Material, Synthetic are used in the following dental and/or surgical procedures: " Alveolar ridge…
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Food)·F-0546-2016·2016-02-17

    Zzang! Original Candy Bar Recalled for Undeclared Soy and Milk

    Zingerman's Candy Manufactory is recalling Zzang! Original Candy Bars due to undeclared soy and milk allergens.

    Product
    Zzang! Original Candy Bar, 2.5 oz., packaged in preprinted cardboard boxes, UPC 8 44397 00014 0
    Category
    Food
    Distribution
    18 states
  • HighFDA (Food)·F-0548-2016·2016-02-17

    Zingerman's Wowza Candy Bar Recalled for Undeclared Soy and Milk

    Zingerman's Candy Manufactory is recalling 1,499 Wowza Candy Bars due to undeclared soy and milk ingredients.

    Product
    Zzang! Wowza Candy Bar,3 oz., packaged in reprinted cardboard boxes, UPC 8 44397 00072 0
    Category
    Food
    Distribution
    18 states
  • HighNHTSA·16V089000·2016-02-17

    Keystone Recalls 2016 Sprinter RVs Due to Falling Television Risk

    Keystone is recalling 2016 Sprinter recreational vehicles because a wall-mounted television may break off, posing an injury risk to occupants.

    Product
    KEYSTONE — KEYSTONE SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0547-2016·2016-02-17

    Zzang! Cashew Cow Candy Bar Recalled for Undeclared Soy

    Zingerman's Candy Manufactory is recalling Zzang! Cashew Cow Candy Bars due to undeclared soy. The product was distributed in 18 states and DC.

    Product
    Zzang! Cashew Cow Candy Bar,2 oz., packaged in reprinted cardboard boxes, UPC 8 44397 00015 7
    Category
    Food
    Distribution
    18 states
  • HighFDA (Drugs)·D-0655-2016·2016-02-17

    Fagron Recalls SyrSpend SF Grape Flavor Due to Yeast Contamination

    Fagron, Inc. is recalling SyrSpend SF Grape Flavor suspending base due to the presence of yeast. The recall affects 148 bottles distributed nationwide.

    Product
    SyrSpend SF, Suspending Base, Grape Flavored, a convenient, sweetened, sugar-free syrup-suspending vehicle specially formulated to assist in extemporaneous preparation of oral liquid dose forms, Rx Only, Shake Well, 4 L bottle, Manufactured by Fagron Inc., St. Paul, MN 55120…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·16104·2016-02-17

    Michaels Recalls Ashland Holiday Paper Boxes Due to Mold Risk

    Michaels is recalling Ashland holiday paper boxes because mold may be present, posing a risk of respiratory or other infections for consumers with compromised immune systems or mold allergies.

    Product
    Ashland® holiday paper boxes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0771-2016·2016-02-17

    Accuray CyberKnife Robotic Recall for Potential Gun Box Mounting Bracket Failure

    Accuray is recalling CyberKnife Robotic systems because the gun box mounting bracket may fail, allowing the gun box to fall and contact a patient.

    Product
    CyberKnife Robotic; Catalog/part number 032000 and 033000 Cosmetic cover package. Product Usage: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy for lesions, tumors, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0761-2016·2016-02-17

    Del Medical VS200 Radiographic Cassette Holder Recall for Falling Hazard

    Del Medical is recalling VS200 radiographic cassette holders and wall stands because they can suddenly fall to the ground and contact patients.

    Product
    VS200 radiographic Cassette Holder or Wall Stand. For use in radiology department.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0763-2016·2016-02-17

    GE Medical Systems Recalls Mavig Monitor Suspension System Due to Fall Risk

    GE Medical Systems is recalling 2,111 Mavig Monitor Suspension Systems because a reported incident involved a suspension arm falling to the floor.

    Product
    Mavig Monitor Suspension System, Model GD60, contained in the following Fluoroscopic imaging systems: Advantx LCV+, Advantx LCN+, Advantx LCLP+, Advantx LCA, INNOVA 2000, INNOVA 4100, INNOVA 3100, INNOVA 3131IQ, INNOVA 2121IQ, INNOVA 2100IQ, INNOVA 3100IQ, and INNOVA 4100IQ
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2016·2016-02-17

    Del Medical VS300 Radiographic Cassette Holder Recall for Falling Hazard

    Del Medical, Inc. is recalling VS300 radiographic cassette holders and wall stands because the unit can suddenly fall to the bottom of its travel and contact a patient.

    Product
    VS300 radiographic Cassette Holder or Wall Stand. For use in radiology department.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0778-2016·2016-02-17

    Zimmer Dental Implants Recalled for Missing Safety Information in Instructions

    Zimmer Dental Inc is recalling specific dental implants because the instructions for use omitted safety information regarding the 3.7 mmD and 4.1 mmD Trabecular Metal models.

    Product
    IMPLANT,TM, MTX FULL 4.1 mm x 10 mm diameter 3.5 mm Catalog #TMT4B10 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0574-2016·2016-02-17

    Bearded Brothers BOLD The Greek Energy Bars Recalled for Mold

    Bearded Brothers LLC is recalling BOLD The Greek energy bars due to mold. The recall covers 150 cases distributed nationwide.

    Product
    Bearded Brothers BOLD The Greek Net Wt. 1.5 oz/43 g UPC: 8-50430-00414-2.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0783-2016·2016-02-17

    Zimmer Dental Implants Recalled for Omitted Safety Information in Instructions

    Zimmer Dental Inc is recalling specific Trabecular Metal dental implants because safety information was missing from the instructions for use.

    Product
    IMPLANT,TM, MTX FULL 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMTB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
    Category
    Medical Device
    Distribution
    Distributed nationwide