The Recall Desk

State

Georgia product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45851–45875 of 83452

  • ModerateFDA (Drugs)·D-0177-2018·2018-01-17

    KRS Global Biotechnology Recalls Human Chorionic Gonadotropin Due to Labeling Errors

    KRS Global Biotechnology is recalling 7,862 vials of Human Chorionic Gonadotropin because the Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    Human Chorionic Gonadotropin 11,000 iu/Vial Lyophilized For SC Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0170-2018·2018-01-17

    KRS Global Biotechnology Recalls Chloramphenicol and Amphotericin Otic Powder

    KRS Global Biotechnology is recalling 20 jars of Chloramphenicol and Amphotericin Otic Powder because the Beyond Use Date exceeds the expiration of at least one ingredient.

    Product
    Chloramphenicol 500 mg Amphotericin 50 mg Otic Powder packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0179-2018·2018-01-17

    KRS Global Biotechnology Recalls Hydroquinone and Tretinoin Ointment Jars

    KRS Global Biotechnology is recalling 30 jars of Hydroquinone 8%/Tretinoin 0.1% Topical Ointment because the Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    Hydroquinone 8%/ Tretinoin 0.1% Topical Ointment packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0184-2018·2018-01-17

    KRS Global Biotechnology Recalls Methylene Blue Injectable Vials for Labeling Errors

    KRS Global Biotechnology is recalling 696 vials of Methylene Blue (PF) 10 mg/mL Injectable due to incorrect or missing lot and expiration dates.

    Product
    Methylene Blue (PF) 10 mg/mL (1%) Injectable Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0207-2018·2018-01-17

    KRS Global Biotechnology Recalls 7-Keto DHEA Capsules Due to Labeling Error

    KRS Global Biotechnology is recalling 7-Keto DHEA 25mg capsules because the Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    7-Keto DHEA 25mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0199-2018·2018-01-17

    KRS Global Biotechnology Recalls Trimix #23F Due to Incorrect Expiration Date

    KRS Global Biotechnology is recalling 94 vials of Trimix #23F because the product's expiration date exceeds the expiration date of at least one ingredient.

    Product
    Trimix #23F (Prostaglandin E1 6 mcg/ Papaverine HCl 17.8 mg/ Phentolamine Mesylate 0.6 mg/mL), For Intracavernous Use, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0201-2018·2018-01-17

    KRS Global Biotechnology Recalls Ophthalmic Solution Due to Labeling Errors

    KRS Global Biotechnology is recalling 297 droptainers of a multi-ingredient ophthalmic solution because the Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    Cyclopentolate HCl/ Phenylephrine HCl/ Tropicamide/ Ketorolac 1%/ 2.5%/ 1%/ 0.5% Ophthalmic Solution, 3 mL Multi Dose Droptainer, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0161-2018·2018-01-17

    KRS Global Biotechnology Recalls Anastrozole 0.5 mg Capsules for Labeling Errors

    KRS Global Biotechnology is recalling 15,700 capsules of Anastrozole 0.5 mg due to incorrect or missing lot and expiration dates.

    Product
    Anastrozole 0.5 mg Capsules, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0168-2018·2018-01-17

    FDA Recalls Bi-Est Cream Due to Expired Ingredient Dates

    KRS Global Biotechnology is recalling 300 jars of Bi-Est Cream because the Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    Bi-Est (Estriol/Estradiol) (80/20) + Progesterone 7.5 mg/200 mg Cream packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0206-2018·2018-01-17

    FDA Recalls 7-Keto DHEA Capsules Due to Expired Ingredient

    KRS Global Biotechnology is recalling 7-Keto DHEA 100 mg capsules because the product's expiration date exceeds the expiration date of at least one ingredient.

    Product
    7-Ketodehydroepiandrosterone (7-Keto DHEA) 100 mg Capsule, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0181-2018·2018-01-17

    KRS Global Biotechnology Recalls Hydroxocobalamin Vials Due to Labeling Errors

    KRS Global Biotechnology is recalling 596 vials of Hydroxocobalamin 1 mg/mL due to incorrect or missing lot and expiration dates.

    Product
    Hydroxocobalamin 1 mg/mL 30 mL Vial For IM Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0196-2018·2018-01-17

    KRS Global Biotechnology Recalls Sermorelin Acetate Vials Due to Labeling Errors

    KRS Global Biotechnology is recalling 157 vials of Sermorelin Acetate/GHRP6 due to incorrect or missing lot and expiration dates.

    Product
    Sermorelin Acetate 3 mg/ GHRP6 3 mg, Lyophilized Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0209-2018·2018-01-17

    Prinston Recalls Valsartan Tablets Due to Physical Specification Failures

    Prinston Pharmaceutical Inc. is recalling 21,987 bottles of Valsartan 160 mg tablets because customer complaints confirmed the tablets were thicker and heavier than specifications.

    Product
    VALSARTAN — VALSARTAN (VALSARTAN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0603-2018·2018-01-17

    Coconuthead Recalls CO YO Chocolate Coconut Yogurt Alternative Due to Container Bloating

    Coconuthead LLC is recalling CO YO Coconut Yogurt Alternative CHOCOLATE because the containers are bloating. The product was distributed nationwide.

    Product
    CO YO Coconut Yogurt Alternative CHOCOLATE, 5.3 oz and 12 oz. plastic container, 6 packages per case. Store between 36 and 42 F. Manufactured by COCONUTHEAD, LLC, Albuquerque NM; Distributed by UNFI and KeHE
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0213-2018·2018-01-17

    Dr. Reddy's Recalls Docetaxel Injection Vials Due to Seal Defects

    Dr. Reddy's is recalling 1,051 vials of Docetaxel Injection USP due to defects in the vial seals that may allow the stopper to detach.

    Product
    DOCETAXEL — DOCETAXEL (DOCETAXEL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0164-2018·2018-01-17

    KRS Global Biotechnology Recalls Topical Cream Due to Expired Ingredient

    KRS Global Biotechnology is recalling 490 jars of Arginine/Lysine/Glutamine Topical Cream because the product's Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    Arginine 150 mg/ Lysine HCl 50 mg/ Glutamine 200 mg/g Topical Cream packaged in jars, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0198-2018·2018-01-17

    KRS Global Biotechnology Recalls Trimix #22F Due to Labeling Errors

    KRS Global Biotechnology is recalling 235 vials of Trimix #22F because the Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    Trimix #22F (Prostaglandin E1 25 mcg/ Papaverine HCl 30 mg/ Phentolamine Mesylate 2 mg/mL), For Intracavernous Use, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0197-2018·2018-01-17

    KRS Global Biotechnology Recalls Sincalide Vials Due to Labeling Errors

    KRS Global Biotechnology is recalling 898 vials of Sincalide 5 mcg due to incorrect or missing lot and expiration dates.

    Product
    Sincalide 5 mcg Lyophilized Vials, For IV Use, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0191-2018·2018-01-17

    KRS Global Biotechnology Recalls QUADMIX #18 Vials Due to Labeling Errors

    KRS Global Biotechnology is recalling 129 vials of QUADMIX #18 because the Beyond Use Date exceeds the expiration date of at least one ingredient.

    Product
    QUADMIX #18, 5 mL Vial, Rx Only, KRS Global Biotechnology, 791 Park of Commerce Blvd, Boca Raton, FL 33487.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0211-2018·2018-01-17

    Akorn Recalls Gabapentin Oral Solution Due to Unapproved Manufacturer

    Akorn Inc is recalling 4,885 bottles of Gabapentin Oral Solution because the product was released with an unapproved active ingredient manufacturer.

    Product
    Gabapentin Oral Solution, 250 mg/5 mL (50 mg/mL) in a 470 mL amber-colored bottle, Rx Only. Manufactured by: Hi-Tech Pharmacal Co., Inc. Amityville, NY 11701. NDC: 50383-311-47
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0153-2018·2018-01-17

    Enoxaparin Sodium Injection Recalled for Labeling Error on Declared Strength

    Sanofi-Aventis is recalling Enoxaparin Sodium injections because a single syringe with a different strength was found in a carton labeled 120 mg/0.8 mL.

    Product
    ENOXAPARIN SODIUM — ENOXAPARIN SODIUM (ENOXAPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalNHTSA·18V038000·2018-01-16

    Mazda Recalls 2006 B-Series Trucks Due to Air Bag Inflator Defect

    Mazda is recalling 2,205 model year 2006 B-Series trucks because the driver-side air bag inflator may explode upon deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide