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.

48451–48475 of 83452

  • SevereFDA (Food)·F-2372-2017·2017-06-28

    Monfitello recalls Private Selection Peri Peri chili paste for peanut content

    Monfitello is recalling Private Selection African-Inspired Peri Peri Chili Culinary Spice Paste because the product may contain peanuts.

    Product
    PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE PASTE NET WT 4 OZ (113g) UPC 0 11110 80699 4 DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Devices)·Z-2224-2017·2017-06-28

    Vascular Solutions Recalls Venture Catheters Due to Material Detachment Risk

    Vascular Solutions, Inc. is voluntarily recalling Venture RX, OTW, and CS catheters because material may detach from the distal tip during use.

    Product
    Venture RX Catheter, Model 5820; Venture OTW Catheter, Model 5821; Venture CS Catheter, Model 5822. Sterilized using ethylene oxide, Rx Only. The Venture catheter is indicated for directing, steering, controlling, and supporting a guidewire to access discrete regions of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2373-2017·2017-06-28

    Monfitello Peruvian Inspired Aji Amarillo Culinary Spice Paste Recalled for Peanut Allergen

    Monfitello is recalling Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste because it may contain peanuts. Consumers should stop using the product.

    Product
    Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET WT 4 OZ (113g) INGREDIENTS: SOY SAUCE***CONTAINS: SOY. DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202 MADE IN CANADA
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Devices)·Z-2616-2017·2017-06-28

    DePuy Mitek LATARJET Coracoid Drill Recalled for Breakage Risk

    DePuy Mitek is recalling LATARJET Coracoid Drills because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Food)·F-2384-2017·2017-06-28

    Genetic Edge Compounds Recalls GEC TNT Thermanite Dietary Supplement

    Genetic Edge Compounds LLC is recalling GEC TNT Thermanite dietary supplements because the product contains DMAA and Methylsynephrine.

    Product
    GEC TNT Thermanite 60 Capsules Dietary Supplement in clear plastic bottle, UPC: 689466706222.
    Category
    Food
    Distribution
    21 states
  • SevereNHTSA·17V410000·2017-06-28

    Lakota Colt Trailers Recalled Due to Furnace Venting Defect

    Lakota Corporation is recalling 2018 Colt trailers because the furnace flue may be improperly installed, preventing proper venting. This defect can cause carbon monoxide buildup inside the trailer, posing a risk of injury or death.

    Product
    LAKOTA — LAKOTA COLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2617-2017·2017-06-28

    DePuy Mitek LATARJET Drill Tip Recall Due to Breakage Risk

    DePuy Mitek is recalling LATARJET Coracoid Top Hat Drills because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: 288202 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-0922-2017·2017-06-28

    Vi-Jon Recalls Magnesium Citrate Saline Laxative Due to Glass Particles

    Vi-Jon, Inc. is recalling 52,212 bottles of Magnesium Citrate Saline Laxative because glass particles were found in the product.

    Product
    Magnesium Citrate Saline Laxative Cherry Flavored, packaged in a) 10 fl. oz. (296 mL) bottle UPC: 072785104556 (Rexall's label), b) 10 fl. oz. (296 mL) bottle UPC: 041163254138 (Equaline's label), OTC, Distributed by a) Dolgencorp, LL, Goodlettsville, TN 37072 b)Supervalu, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·17752·2017-06-28

    Homestar Recalls Three-Drawer TV Chests Due to Tip-Over Hazards

    Homestar North America is recalling about 1,470 Stockholm three-drawer TV chests sold at Target.com because they pose serious tip-over and entrapment hazards to children if not anchored to the wall.

    Product
    Stockholm three-drawer TV chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2386-2017·2017-06-28

    Publix Deli Artichoke and Spinach Dip Recalled for Glass Fragments

    Publix Super Markets is recalling 16-ounce Artichoke & Spinach dip due to potential glass fragments. The product was distributed to six southeastern states.

    Product
    Publix Deli, Artichoke & Spinach dip, 16 oz., plastic clamshell, Manufactured and distributed by Publix Super Markets, Lakeland, FL.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2619-2017·2017-06-28

    DePuy Mitek LATARJET Extraction Driver Recalled for Breakage Risk

    DePuy Mitek is recalling 115 units of the LATARJET EXPERIENCE Extraction Driver because the tip may break during surgery when used at an angle.

    Product
    DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-2618-2017·2017-06-28

    DePuy Mitek Top Hat Tap Screw Driver Tip Recall

    DePuy Mitek is recalling 153 units of the LATARJET EXPERIENCE Top Hat Tap because the Combo Screw Driver tip may break during surgery.

    Product
    DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighNHTSA·17V409000·2017-06-28

    KME Predator Tanker Recalled for Fuel Pump Drive Gear Slip

    Kovatch Mobile Equipment is recalling one 2017 KME Predator Tanker truck because a fuel pump drive gear may slip, causing an engine stall that increases crash risk.

    Product
    KME — KME PREDATOR TANKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2615-2017·2017-06-28

    DePuy Mitek LATARJET Combo Screw Driver Recalled for Breakage Risk

    DePuy Mitek is recalling 173 LATARJET Combo Screw Drivers because the tip may break during surgery when used at an angle.

    Product
    DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior glenoid with a bony graft
    Category
    Medical Device
    Distribution
    8 states
  • HighNHTSA·17V407000·2017-06-28

    Lance Recalls 2018 Travel Trailers with Defective Utility Receivers

    Lance is recalling 2018 Travel Trailers with optional utility receivers that have insufficient welds, which may cause attached items to contact the road.

    Product
    LANCE — LANCE TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2613-2017·2017-06-28

    Abbott Recalls ARCHITECT SHBG Reagent Due to Specimen Tube Interference

    Abbott Laboratories is recalling 7,981 kits of ARCHITECT SHBG Reagent because using Potassium EDTA specimen tubes may cause falsely decreased test results.

    Product
    ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent microparticle immunoassay (CMIA) for the quantitative determination of sex hormone binding globulin (SHBG) in human serum and plasma on the ARCHITECT iSystem. The ARCHITECT SHBG assay is used as an aid in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0921-2017·2017-06-28

    Lucid Pharma Recalls Venlafaxine Hydrochloride Extended-Release Capsules Due to Melted Capsules

    Lucid Pharma LLC is recalling specific lots of Venlafaxine Hydrochloride Extended-Release Capsules, 75 mg, because pharmacists reported bottles containing melted capsules.

    Product
    Venlafaxine Hydrochloride Extended-Release Capsules USP, 75 mg, packaged in a) 30-count bottles (NDC 52343-132-30) and b) 90-count bottles (NDC 52343-132-90), Rx only, Distributed by: Lucid Pharma LLC, 2 Tower Center Blvd, Suite-1101-B, East Brunswick, NJ 08816 USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2612-2017·2017-06-28

    Z-Medica Recalls QuikClot TraumaPad Due to Packaging Sterility Concerns

    Z-Medica is recalling 2,910 units of QuikClot TraumaPad hemostatic dressings because packaging breaches may compromise sterility.

    Product
    QuikClot TraumaPad, , sterile, soft, white, X-ray detectable hemostatic dressing Part Number 460 Manufactured by Z-Medica, LLC 4 Fairfield Boulevard, Wallingford, CT 06492 USA For use as a topical dressing for local management of bleeding wounds such as cuts, lacerations…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2601-2017·2017-06-28

    Merge OrthoPACS software recalled due to data propagation failures

    Merge Healthcare is recalling specific versions of Merge OrthoPACS software because studies may fail to transfer or import correctly between servers.

    Product
    Merge OrthoPACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2620-2017·2017-06-28

    Merge OrthoPACS Software Recalled for Annotation Display Error

    Merge Healthcare is recalling Merge OrthoPACS software versions 6.6, 6.6.1, and 6.6.2 because prior studies may fail to display annotations.

    Product
    Merge OrthoPACS software.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·17181·2017-06-27

    TNT Red, White, & Blue Smoke Fireworks Recalled for Burn Hazards

    American Promotional Events is recalling TNT Red, White, & Blue Smoke fireworks because they can explode unexpectedly, causing burn injuries.

    Product
    TNT Red, White, & Blue Smoke fireworks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V403000·2017-06-27

    Spartan Recalls 2017-2018 Chassis Due to Fuel Pump Gear Slip Risk

    Spartan Motors is recalling 2017-2018 K3, K4, and Gladiator chassis because a fuel pump gear may slip, causing engine stalls that increase crash risk.

    Product
    SPARTAN — SPARTAN K3, GLADIATOR, K4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V405000·2017-06-27

    Triple E RV Recalls 2017 Wonder Motorhomes Due to Fire Risk

    Triple E RV is recalling 35 units of the 2017 Wonder motorhome because the water heater door can block the furnace, increasing fire risk.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V404000·2017-06-27

    GM Recalls 2016-2017 Buick Envision for Head Restraint Defect

    General Motors is recalling 2016-2017 Buick Envision vehicles because incorrectly installed tablet holders may prevent head restraints from fully engaging, increasing injury risk in a crash.

    Product
    BUICK — BUICK ENVISION
    Category
    Vehicle
    Distribution
    Distributed nationwide