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.

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.

49551–49575 of 83452

  • SevereFDA (Drugs)·D-0683-2017·2017-05-03

    Isomeric Pharmacy Recalls Triamcinolone Acetonide Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,335 vials of Triamcinolone Acetonide and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Triamcinolone Acetonide 40 mg/mL, Lidocaine HCl 10 mg/mL , 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1020, barcode 3 70285 10201 1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0677-2017·2017-05-03

    FDA Recalls Unapproved hCG Body Shaper Product for Contamination

    The FDA is recalling hCG Body Shaper because it was marketed without approval and contains human chorionic gonadotropin, making it an unapproved drug.

    Product
    hCG Body Shaper, Highly Purified Human Chorionic Gonadotrophin 5000 IU, Colloidal Silver B12, Stabilizers/Excipients, Not For Medical Use, Must Be Refrigerated, Distributed by HCG Body Shaper, St. Peters, MO
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1832-2017·2017-05-03

    HeartWare HVAD Pump Driveline Splice Kit Recall for Improved Repair

    Medtronic is notifying clinicians that an improved splice kit is available to replace the HeartWare HVAD Pump Driveline Splice Kit due to a safety issue.

    Product
    HeartWare Ventricular Assist System (HVAD) Pump Driveline Splice Kit Product Usage: Is intended to repair the driveline cable once an electrical break has been identified. These repairs are limited to the portion of the driveline that is outside the patient boundary (exit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2106-2017·2017-05-03

    Guggisberg Pepper Jack Cheese Recalled for Listeria Risk

    Guggisberg Cheese Inc is recalling specific lots of Pepper Jack Cheese because the product may contain Listeria monocytogenes.

    Product
    Pepper Jack Cheese sold under the following brand names: Amish Classic 6 lb, Dutch Farms 6 lb, Guggisberg 6 lb, 14 lb, Mini Rounds & Long Horn & Walnut Creek 6 lb
    Category
    Food
    Distribution
    13 states
  • SevereNHTSA·17V297000·2017-05-03

    Audi Recalls 2017 Q5 Vehicles Due to Gearbox Defect

    Volkswagen Group of America is recalling 2017 Audi Q5 vehicles because a gearbox defect may allow the vehicle to roll unexpectedly while in Park.

    Product
    AUDI — AUDI Q5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2107-2017·2017-05-03

    Guggisberg Thunder Jack Cheese Recalled for Listeria Risk

    Guggisberg Cheese Inc is recalling Thunder Jack Cheese sold as Amish Classic Firecracker due to potential Listeria monocytogenes contamination.

    Product
    Thunder Jack Cheese sold under the following brand names: Amish Classic Firecracker & Guggisberg
    Category
    Food
    Distribution
    13 states
  • SevereNHTSA·17V289000·2017-05-03

    Porsche Recalls Macan Models Due to Fuel Pump Flange Crack Risk

    Porsche is recalling 2015-2017 Macan models because a fuel pump flange may crack, causing a fuel leak that increases fire risk.

    Product
    PORSCHE — PORSCHE MACAN S, MACAN TURBO, MACAN, MACAN GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0682-2017·2017-05-03

    Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,352 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Methylprednisolone Acetate 80 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1011, barcode 3 70285 10111 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1538-2017·2017-05-03

    Heartware Recalls HVAD System Controllers for Exchange

    Heartware is recalling all HVAD System Controllers currently on the market to exchange them for the next generation HVAD Controller (Controller 2.0).

    Product
    HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare Ventricular Assist System…
    Category
    Medical Device
    Distribution
    37 states
  • SevereFDA (Food)·F-2099-2017·2017-05-03

    Guggisberg Cheese Recalls Butter Cheese for Potential Listeria Contamination

    Guggisberg Cheese Inc is recalling Amish Creamery Butter Cheese because it may contain Listeria monocytogenes. The product was distributed to 13 states.

    Product
    Amish Creamery Butter Cheese Sold under the following brand names: Amish Classic 6 lb & 15 ib and Guggisberg 15 ib Distributed by: Guggisberg Cheese, 5060 S.R. 557, Millersburg, OH 44654
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-2103-2017·2017-05-03

    Guggisberg Garden Vegetable Natural Cheese Recalled for Listeria Risk

    Guggisberg Cheese Inc is recalling Garden Vegetable Natural Cheese because it may contain Listeria monocytogenes. The product was distributed to 13 states.

    Product
    GUGGISBERG GARDEN VEGETABLE NATURAL CHEESE INGREDIENTS: Pasterized Milk, Cultures, Red & Green Pell Peppers, Parsley, Salt, Onion, Celery, Carrots, Cucumbers, Califlower, Enzymes, LIve Yogurt Cultures 11275 W 250 N MIDDLEBURY, IN 46540
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0686-2017·2017-05-03

    Isomeric Pharmacy Recalls Testosterone Injection Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 2,156 vials of Testosterone Cypionate and Propionate injection due to production processes that cannot assure sterility.

    Product
    Testosterone Cypionate 200 mg/mL, Testosterone Propionate 20 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Dr, SLC, UT 84109, Part # 1200, barcode 3 70285 12003 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V298000·2017-05-03

    Audi Recalls Q5 and Q7 Models for Fuel Pump Flange Crack Risk

    Volkswagen Group of America is recalling 2013-2017 Audi Q5 and Q7 vehicles because a fuel pump flange may crack, allowing fuel to leak and increasing fire risk.

    Product
    AUDI — AUDI Q5, Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2101-2017·2017-05-03

    Guggisberg Cheese Recalls Colby Cheese for Potential Listeria Contamination

    Guggisberg Cheese Inc is recalling Colby Cheese sold under multiple brands due to potential Listeria monocytogenes contamination.

    Product
    Colby Cheese sold under the following brand names: Amish Classic 6lb & 15lb, Dietz & Watson 6lb, Dutch Farms 6lb, Guggisberg 8oz, 12oz, 1ib, 6lb, 14lb & 15lb, Lipari 6lb & 15lb, Meijer & Walnut Creek 6lb & 15lb
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-0685-2017·2017-05-03

    Isomeric Pharmacy Recalls Injection Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 851 vials of a multi-dose injection product because production processes cannot assure sterility.

    Product
    Cyanocobalamin 1 mg/mL/ Methionine 25 mg/mL/ Inositol 50 mg/mL/ Choline 50 mg/mL, 30 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1101, barcode 3 70285 11013 9.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0681-2017·2017-05-03

    Isomeric Pharmacy Recalls Methylprednisolone Acetate Injection Vials for Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 4,001 vials of Methylprednisolone Acetate and Lidocaine HCl injection due to production processes that cannot assure sterility.

    Product
    Methylprednisolone Acetate 40 mg/mL, Lidocaine HCl 10 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1010, barcode 3 70285 10101 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2095-2017·2017-05-03

    ConAgra Recalls Premium Hunt's Chili Kits for Potential Salmonella

    ConAgra Foods is recalling Premium Hunt's Chili Kits due to potential Salmonella contamination in the spice packets. The recall covers 5,458 cases distributed nationwide.

    Product
    Premium Hunt's Chili Kit, Total NET WT 44.8 OZ (2.80 LB) 1.27kg; Directions: 1) Cook and stir meat in saucepan over medium-high 7 minutes or until done; drain. 2) Stir in all remaining ingredients; simmer 10 minutes, stirring occasionally. Con Agra Foods, P.O BOX 3768, Dept.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1888-2017·2017-05-03

    Remel Blood Agar Plates Recalled for Listeria Contamination

    Remel Inc is recalling Blood Agar plates due to confirmed surface contamination with Listeria monocytogenes. The products were distributed nationwide and in Puerto Rico.

    Product
    Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood Agar is a solid medium recommended for use in qualitative procedures for the cultivation of a wide variety of microorganisms and visualization of hemolytic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2139-2017·2017-05-03

    Roundy's and Harris Teeter Hash Browns Recalled for Golf Ball Material

    McCain Foods USA is recalling Roundy's and Harris Teeter Southern Style Diced Hash Browns because they are contaminated with extraneous golf ball material.

    Product
    Roundy's Southern Style Diced Hash Browns, frozen, net wt. 32 oz per package, UPC 0 01115 05501 9. Harris Teeter Southern Style Diced Hash Browns, frozen, net wt. 32 oz per package, UPC 0 07203 64902 0.
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1877-2017·2017-05-03

    Cardiovascular Systems Recalls ViperWire Advance Guide Wires Due to Packaging Error

    Cardiovascular Systems Inc is recalling 595 units of ViperWire Advance guide wires because 0.018-inch products were packaged as 0.014-inch.

    Product
    ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14. Product Usage: The Stealth 360 Orbital PAD System and the Diamondback 360 Peripheral Orbital Atherectomy System are percutaneous orbital atherectomy systems…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1878-2017·2017-05-03

    Ulrich Medical Recalls uNion Cervical Plate System for Screw Mechanism Defect

    Ulrich Medical USA Inc is recalling 4,854 uNion Cervical Plate Systems because static plate screws may disassociate. The recall covers devices distributed in 20 US states.

    Product
    uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the cervical spine (C2 to Ti). The system is to be used to provide stabilization of the anterior cervical spine as an adjunct to fusion for the treatment of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0684-2017·2017-05-03

    Isomeric Pharmacy Recalls Triamcinolone Diacetate Vials Due to Sterility Concerns

    Isomeric Pharmacy Solution, LLC is recalling 1,951 vials of Triamcinolone Diacetate injection because production processes cannot assure sterility. The FDA has classified this as a Class II recall.

    Product
    Triamcinolone Diacetate 40 mg/mL, 10 mL Multi-Dose Vial For Injection, Rx Only, Isomeric Pharmacy Solutions, 2401 Foothill Drive, SLC, UT 84109, Part # 1021, barcode 3 70285 10211 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1889-2017·2017-05-03

    Merit Medical Recalls 1 mL Medallion Syringes Due to Plunger Tip Defect

    Merit Medical Systems is voluntarily recalling 1 mL Medallion Syringes because of a defect in the syringe plunger tip.

    Product
    1 mL Medallion¿ Syringe. Catalog Numbers: 701989001, K01-05197P, MSS011-YP, K01-07946P, MSS011, MSS011-LB, MSS011-R, MSS011-Y, MSS011P, MSS011-LBP, MSS011-DG, K08-02926AP, K01-07742P, K10-05457P.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1884-2017·2017-05-03

    XTANT Medical Recalls 5.5mm CoCr Straight Rods Due to Labeling Error

    XTANT Medical Inc. is recalling 97 units of 5.5mm CoCr Straight Rods because the labels may incorrectly identify the material as Ti6Al-4V ELI instead of Cobalt Chromium.

    Product
    5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one piece per bag. Product Usage: The 5.5mm dia. X 500 mm CoCr Straight Rod is an accessory to the Fortex Pedicle Screw System. It is a straight rod connected…
    Category
    Medical Device
    Distribution
    Distributed nationwide