The Recall Desk

State

Georgia product recalls

73,741 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,632
Critical
1,471
Severe
2,565
Most recent
2026-10-28

Of the 9,632 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 2,565 (27%) are Severe.

These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38751–38775 of 83373

  • ModerateFDA (Drugs)·D-1113-2019·2019-04-17

    Gavilyte-N Recalled for Incorrect Flavor Labeling on Orange and Cherry Packets

    Lupin Somerset is recalling Gavilyte-N because orange and cherry flavor packets incorrectly list 'natural lemon flavor' as an ingredient.

    Product
    GAVILYTE-N — GAVILYTE-N (POLYETHYLENE GLYCOL-3350, SODIUM CHLORIDE, POTASSIUM CHLORIDE AND SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1243-2019·2019-04-17

    Newly Weds Foods Recalls Commercial Breader Batter Due to Plastic Contamination

    Newly Weds Foods is recalling 20,000 lbs of commercial breader batter that may contain small pieces of plastic. The product was distributed to commercial processors in 14 states.

    Product
    Commercial Breader Batter; A28986 BATTER MX X1; 50 pound bag
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1089-2019·2019-04-17

    Integra bioBLOCK Resorbable Subtalar Implant Recalled for Temperature Exposure

    Integra Limited is recalling 232 units of the bioBLOCK Resorbable Subtalar Implant because temperature indicators suggest exposure to temperatures above 110°F.

    Product
    Integra bioBLOCK Resorbable subtaler Implant, 10mm Catalog Number: 40010 - Product Usage: The bioBLOCK Implant is indicated for internal support to primary surgical interventions in the treatment of flatfoot.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1275-2019·2019-04-17

    Walgreens Probiotic Recalled for Incorrect Bacterial Strain

    Merical, LLC is recalling Walgreens Probiotic 12.5 Billion Active Cultures because the product contains a different bacterial strain than listed on the label.

    Product
    Walgreens Probiotic 12.5 Billion Active Cultures, 30 capsules; Dietary Supplement. Probiotic Blend 12.5 Billion CFU's L. rhamnosus HN001, L acidophilus La-14, L reuteri L.RE02. Other ingredients: Cellulose, Gelatin, Silicon Dioxide, Magnesium Stearate (vegetable…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1084-2019·2019-04-17

    X-Gen Recalls Clonidine Injection Vials Due to Labeling Error

    X-Gen Pharmaceuticals is recalling Clonidine HCL Injection vials because the side carton incorrectly lists the concentration as 500 mcg instead of 100 mcg per mL.

    Product
    CLONIDINE — CLONIDINE (CLONIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1082-2019·2019-04-17

    Auro Pharmacies Recalls Biotin Injection Vials for pH Failure

    Auro Pharmacies Inc. is recalling 167 vials of Biotin 10 mg/mL Injection because the product failed to meet its pH label claim.

    Product
    Biotin 10 mg/mL Injection, 30 mL vial, Rx only, 511 S. Harbor Blvd., Building. F, La Habra, CA 90631, 562-352-9630.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1134-2019·2019-04-17

    GE Healthcare Recalls Thallous Chloride TI 201 Injection Due to Chemical Contamination

    Medi-Physics Inc. dba GE Healthcare is recalling Thallous Chloride TI 201 Injection vials because trace amounts of an impurity were detected in the manufacturing reagent.

    Product
    Thallous Chloride TI 201 Injection, Specific Concentration: 37 MBq/mL (1 mCi/mL), Total Activity: 325.6 MBq (8.8 mCi) Volume: 8.8 mL vial, Rx Only, Mfg. by GE Healthcare, Medi-physics, Inc., Arlington Heights, IL 60004. NDC: 17156-299-18
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V306000·2019-04-16

    2019 Fleetwood and Holiday Rambler Motorhomes Recalled for Exhaust Defect

    REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER FLAIR, ADMIRAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E029000·2019-04-15

    Triumph Recalls Thruxton Motorcycles Due to Wiring Clearance Issue

    Triumph is recalling 2016-2018 Thruxton motorcycles because accessory fairing kits may damage wiring, causing loss of lights or engine stalls.

    Product
    TRIUMPH — TRIUMPH THRUXTON 1200R, THRUXTON 1200, THRUXTON A2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·19105·2019-04-12

    Fisher-Price Recalls Rock 'n Play Sleepers Due to Infant Death Reports

    Fisher-Price is recalling all Rock 'n Play Sleepers because over 30 infant fatalities have occurred. Consumers should stop using the product immediately and contact the company for a refund.

    Product
    All Models of Rock 'n Play Sleeper
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V298000·2019-04-12

    Honda and Acura Recall Vehicles Due to Timing Belt Defect

    Honda is recalling specific 2018-2019 Acura and Honda vehicles because timing belt teeth may separate, potentially causing an engine stall and increasing crash risk.

    Product
    HONDA — HONDA, ACURA PILOT, TLX, ODYSSEY, RIDGELINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V299000·2019-04-12

    Honda Recalls 2018-2019 Odyssey for Transmission Control Unit Reboot Risk

    Honda is recalling 2018-2019 Odyssey vehicles because loose battery connections may cause the transmission to shift to Park, potentially damaging the parking rod and increasing crash risk.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E028000·2019-04-12

    Cush Corp Recalls Trailer Axles Due to Wheel Separation Risk

    Cush Corp is recalling specific trailer suspension systems because a locking device may not be installed properly, allowing the wheel end to separate from the axle.

    Product
    SUSPENSION:REAR:AXLE:NON-POWERED AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V293000·2019-04-11

    Chrysler Recalls 2013-2016 Dodge Dart Vehicles for Shifter Cable Defect

    Chrysler is recalling 2013-2016 Dodge Dart vehicles with 6-speed automatic transmissions because the shifter cable bushing may fail, allowing the cable to detach and increasing crash risk.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide