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.

57076–57100 of 83468

  • SevereNHTSA·16V113000·2016-02-26

    Chrysler Recalls 2015-2016 Dodge Dart Vehicles for Software Defect

    Chrysler is recalling certain 2015 and 2016 Dodge Dart vehicles because a missing software backup in the powertrain control module may increase the risk of a crash.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V115000·2016-02-26

    Open Range Recalls 2012-2014 Trailers Due to Incorrect Weight Labels

    Open Range is recalling 2012-2014 Mesa Ridge, Roamer, and Light trailers because incorrect Gross Vehicle Weight Rating labels may lead to overloading.

    Product
    OPEN RANGE — OPEN RANGE LIGHT, ROAMER, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V109000·2016-02-25

    Honda Recalls 2014 NSS300 Scooters for Rear Brake Line Leak

    Honda is recalling 2014 NSS300 and NSS300A scooters because improperly tightened rear brake lines may leak fluid, reducing braking function and increasing crash risk.

    Product
    HONDA — HONDA FORZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V112000·2016-02-25

    Open Range Journeyer Trailers Recalled for Underrated Safety Chains

    Open Range is recalling 2012-2015 Journeyer trailers because the safety chains are not rated high enough to support the trailer's weight if the main connection fails.

    Product
    OPEN RANGE — OPEN RANGE JOURNEYER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V110000·2016-02-25

    Ford Recalls 2016 F-150 Trucks Due to Air Bag Sensor Defect

    Ford is recalling 2016 F-150 trucks with Multi-Contour Seats because the passenger air bag sensor may misclassify adults as children, preventing air bag deployment.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V111000·2016-02-25

    Ford Recalls 2015-2016 Transit Vehicles for Rear Seat Belt Defect

    Ford is recalling 2015-2016 Transit vans because rear seat belt buckles may fail to latch if damaged by heavy objects, increasing crash injury risk.

    Product
    FORD — FORD TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0672-2016·2016-02-24

    Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients

    Premiere Sales Group is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.

    Product
    Rhino 7 3000, 6 count Bottle, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0674-2016·2016-02-24

    Medisca Recalls L-Citrulline API Due to Labeling Error

    Medisca Inc is recalling L-Citrulline API bottles because FDA testing found the product contained N-acetyl-leucine instead of the labeled ingredient.

    Product
    CITRULLINE (L) in 25 g, 100 g, 500 g and 1 kg plastic bottles, White crystals or crystalline powder, odorless, For Use and distribution in prescription compounding, manufacturing, processing, or repackaging only in accordance with FDA regulations and applicable law, Packaged by…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0671-2016·2016-02-24

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    MSNV, Inc dba National Video Supply is recalling Rhino 7 Platinum 3000 single blister packs because they contain undeclared active pharmaceutical ingredients.

    Product
    Rhino 7 Platinum 3000, Single Blister Packs, distributed By Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0669-2016·2016-02-24

    Glades Drugs Recalls Vitamin D3 Supplement Due to Excessive Potency

    Glades Drugs Inc. is recalling Vitamin D3 supplement capsules because they contain an extremely high level of vitamin D3.

    Product
    Vitamin Supplement (Vial) D3, (cholecalciferol (vit D3)/lipoic acid/ubiquinol/ methylcobalamin/pyridoxine/methionine/inositol/choline bitartrate USP) capsules, 60, 120 or 180 count vials, Glades Drugs, 109 S. Lake Ave., Pahokee, FL 33476.
    Category
    Drug
    Distribution
    2 states
  • CriticalFDA (Drugs)·D-0667-2016·2016-02-24

    APEXXX tablets recalled for containing unapproved sildenafil

    Nuway Distributors is recalling APEXXX tablets because they contain sildenafil, an unapproved drug for erectile dysfunction.

    Product
    APEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway Distributors, LLC, Orlando, FL USA; UPC 7 05105 96361 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0664-2016·2016-02-24

    Akttive Fat Burner Recalled for Undeclared Dangerous Ingredients

    Life and More LLC is recalling Akttive High Performance Fat Burner Gold capsules because FDA testing found undeclared sibutramine, desmethylsibutramine, and phenolphthalein.

    Product
    Akttive High Performance Fat Burner Gold dietary supplement capsules, 30-count bottle, Distributed by Life and More, L.L.C., Doral, Florida
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0673-2016·2016-02-24

    Rhino 7 Platinum 3000 Recalled for Undeclared Active Ingredients

    FDA recalls Rhino 7 Platinum 3000 because it contains undeclared active pharmaceutical ingredients, desmethyl carbondenafil and dapoxetine.

    Product
    Rhino 7 Platinum 3000, 1 count Blister Pack, Distributed by Rhino 7, Made in USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0662-2016·2016-02-24

    Medline Recalls Mislabeled Acetaminophen Extra-Strength Pain Reliever Tablets

    Medline Industries is recalling 500 mg acetaminophen tablets mislabeled as 325 mg. Consumers should stop using the product and return it to the retailer.

    Product
    ACETAMINOPHEN EXTRA-STRENGTH PAIN RELIEVER tablets, 500 mg, 100-count bottle, Distributed by Medline Industries, Inc., Mundelein, ILL 60060, NDC 53329-641-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0675-2016·2016-02-24

    Inaffit Recalls Natureal Burn Fat Nature Due to Undeclared Sibutramine

    Inaffit, LLC is recalling Natureal Burn Fat Nature capsules because the product contains undeclared sibutramine and was marketed without an approved NDA or ANDA.

    Product
    NATUREAL BURN FAT NATURE, 30-count capsules, packaged in clear plastic bottle, Manufactured for: Inaffit, LLC. P.O. Box 34056, Bethesda, MD 20827.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0722-2016·2016-02-24

    Fit Firm and Fabulous Recalls Ultimate Herbal Slimcap Capsules

    Fit Firm and Fabulous is recalling Ultimate Herbal Slimcap Capsules because they contain undeclared sibutramine, a controlled substance removed from the U.S. market for safety reasons.

    Product
    Ultimate Herbal Slimcap Capsules, 350 mg*, 30-count bottles, labeled Part 1 of 3, fit firm & fabulous, UPC 5 42423 25422 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0668-2016·2016-02-24

    Hospira Recalls Magnesium Sulfate Injection Bags Due to Incorrect Barcode Labeling

    Hospira is recalling 213,600 bags of Magnesium Sulfate in Water for Injection because the primary bag labeling may be mislabeled with a barcode that scans as heparin sodium.

    Product
    MAGNESIUM SULFATE IN WATER — MAGNESIUM SULFATE IN WATER (MAGNESIUM SULFATE IN WATER)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0670-2016·2016-02-24

    Rhino 7 3000 Recalled for Undeclared Active Pharmaceutical Ingredients

    MSNV, Inc dba National Video Supply is recalling Rhino 7 3000 bottles because they contain undeclared active pharmaceutical ingredients.

    Product
    Rhino 7 3000, 6 count bottles, Distributed by Rhino 7, Made in USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0819-2016·2016-02-24

    Medtronic Recalls Endo GIA Ultra Universal Short Stapler Handles

    Medtronic is recalling 364,768 Endo GIA Ultra Universal Short Stapler Handles because they may fail to fire or partially fire, and the articulating lever may disengage during use.

    Product
    Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Ref: EGIAUSHORT Product Usage: The Endo GIA Ultra Universal Short, Endo GIA Ultra Universal and Endo GIA Ultra Universal XL staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V108000·2016-02-24

    GM Recalls 2016 Buick Regal for Power Steering Failure Risk

    General Motors is recalling 2016 Buick Regal vehicles because the power-steering assist system may fail, increasing crash risk.

    Product
    BUICK — BUICK REGAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0822-2016·2016-02-24

    Medtronic Recalls Endo GIA Ultra Universal Stapler Handles in Best Practice Kits

    Medtronic is recalling 2,711 Best Practice Kits containing specific Endo GIA Ultra Universal Stapler Handles due to reports of staplers failing to fire or partially firing, and articulating levers disengaging during use.

    Product
    Best Practice Kits containing certain production lots of Endo GIA Ultra Universal Stapler Handles Product Usage: The Endo GIA Ultra Universal Short, Endo GIA Ultra Universal and Endo GIA Ultra Universal XL staplers have applications in abdominal, gynecologic, pediatric and…
    Category
    Medical Device
    Distribution
    Distributed nationwide