The Recall Desk

State

Georgia product recalls

73,187 recalls have nationwide distribution and so reach Georgia. 9,619 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,619
Critical
1,474
Severe
2,177
Most recent
2026-09-25

Of the 9,619 recalls naming Georgia we have scored against our rubric, 1,474 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,177 (23%) are Severe.

These figures cover only the 9,619 recalls whose distribution notice names Georgia specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12851–12875 of 82806

  • HighFDA (Devices)·Z-1488-2024·2024-04-17

    Medline SwivAssist Bed Assist Bars Recalled for Safety Standard Non-Compliance

    Medline is recalling 79 Bed Assist Bars that failed to comply with federal safety standards for adult portable bed rails. The products were manufactured after the compliance deadline.

    Product
    Bed Assist Bars, labeled as follows: a) Medline SwivAssist Bar, Model Number MDS6800SWIV (case of 3), b) Medline SwivAssist Bar, Model Number MDS6800SWIVRH (individual)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1508-2024·2024-04-17

    Nucleic Acid Isolation Device Recall: EZ2 Connect MDx-IVD Heater Failure

    Qiagen Sciences is recalling 168 units of the EZ2 Connect MDx-IVD nucleic acid isolation device due to insufficient welding that causes heater cable embrittlement and device malfunction, resulting in sample loss during testing.

    Product
    EZ2 Connect MDx-IVD Designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model Number: 9003230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V272000·2024-04-17

    Forest River Travel Trailers LED Backlight Circuit Board Fire Risk

    Forest River and Dynamax are recalling multiple 2018–2024 travel trailer models due to LED backlight circuit boards in cooktop ranges that may overheat and create a fire risk. Dealers will disconnect and remove the LED backlight wiring at no charge.

    Product
    FOREST RIVER — FOREST RIVER, DYNAMAX IBEX, DX3, CEDAR CREEK, WILDCAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1516-2024·2024-04-17

    PEG feeding tube with blocked connector may impede placement procedure

    Boston Scientific's EndoVive 20Fr PEG Kit may have a blocked connector that prevents the guidewire from advancing during placement, potentially causing complications including bleeding and aspiration.

    Product
    EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00568211
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1482-2024·2024-04-17

    RayStation Software Use Error Could Cause Incorrect Radiation Dose Calculations

    RayStation radiation therapy planning software versions 8B through 2024A contain a use error that can incorrectly select silicon material for silicone gel polymer implant dose calculations, potentially resulting in incorrect radiation doses.

    Product
    RayStation Software Version Numbers version numbers 8B, 9A, 9B, 10A, 10B, 11A, 11B, 12A, 12B, 2023B, 2024A including some service packs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1148-2024·2024-04-17

    Deluxe brand Macarons Party Edition recalled for undeclared allergens

    Lidl is recalling Deluxe Macarons Party Edition due to undeclared allergens. The packaging is labeled in a foreign language and does not identify wheat, soy, egg, milk, and tree nuts.

    Product
    Deluxe brand Macarons Party Edition 35 pieces 455g (35 x 13g) UPC:4056489365365 Product packaged in a cardboard/plastic container
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1497-2024·2024-04-17

    Acetabular Bearing Components Recalled for Marketing Without FDA Clearance

    Synovo Production is recalling 1,681 acetabular bearing components that were marketed without FDA clearance.

    Product
    ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020, STERILEEO, Reference Numbers: 01-02-4254 01-02-4456 01-02-4558 01-02-4760 01-02-4962 01-02-5164 01-02-5266
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1126-2024·2024-04-17

    SWAD Cinnamon Powder Recalled Due to Lead Contamination

    RAJA FOODS LLC is recalling SWAD BRAND CINNAMON POWDER (3.5 oz) after testing confirmed lead contamination. The affected batch should not be consumed.

    Product
    SWAD BRAND CINNAMON POWDER in clear plastic 3.5 OZ bags, UPC 0-51179-34280-4, 20 retail units per wholesale case
    Category
    Food
    Distribution
    15 states
  • HighNHTSA·24V275000·2024-04-17

    Lexus LS Air Bag Sensor May Fail to Detect Front Passenger

    Toyota is recalling certain 2018–2021 Lexus LS and LS Hybrid vehicles with the Executive Package because the front passenger seat occupant sensor may fail to detect a passenger, risking improper air bag deployment in a crash.

    Product
    LEXUS — LEXUS LS HYBRID, LS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1513-2024·2024-04-17

    EndoVive 20Fr Push Safety PEG Kit Recall Due to Blocked Lumen Risk

    Boston Scientific is recalling the EndoVive 20Fr PEG feeding kit due to blockage in the barb connector that can prevent proper placement. The blockage may lead to prolonged procedures, bleeding, gastric leakage, and aspiration risk.

    Product
    EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1138-2024·2024-04-17

    Hashbrown Casserole Recalled Due to Missing Ingredient Labeling

    Robeson Enterprises is recalling Pies & Sides Hashbrown Casserole because the label lacks an ingredient list, preventing consumers from identifying allergens. The product was distributed in Georgia, North Carolina, and South Carolina.

    Product
    PIES & SIDES HASHBROWN CASSEROLE, ALLERGENS: MILK, WHEAT, SOY, FISH, PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1133-2024·2024-04-17

    PIES & SIDES Broccoli Casserole Recalled for Missing Ingredient Labels

    PIES & SIDES Broccoli Casserole by Robeson Enterprises is recalled because the product label does not list ingredients. The product contains wheat, eggs, milk, soy, and fish.

    Product
    PIES & SIDES Broccoli Casserole Contains: Wheat, Eggs, Milk, Soy, Fish PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1514-2024·2024-04-17

    PEG Feeding Tube Kit Recalled for Blocked Lumen Preventing Guidewire Advancement

    Boston Scientific is recalling 572 EndoVive PEG feeding tube kits due to a blocked lumen in the barb connector that may prevent guidewire advancement during placement, potentially requiring device exchange and increasing risk of complications.

    Product
    EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509051
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1144-2024·2024-04-17

    Squash casserole recalled for missing ingredient and allergen labeling

    Robeson Enterprises is recalling its Pies & Sides squash casserole due to missing ingredient list labeling. The product contains undisclosed allergens (milk, eggs, soy, fish, wheat).

    Product
    PIES & SIDES SQUASH CASSEROLE CONTAINS: MILK, EGGS, SOY, FISH, WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1146-2024·2024-04-17

    Sweet Potato Casserole Recall Due to Missing Ingredient Labels

    Robeson Enterprises is recalling Pies & Sides Sweet Potato Casserole because the product label fails to list any ingredients, including egg and milk. Consumers with allergies to these ingredients should not consume the product.

    Product
    PIES & SIDES SWEET POTATO CASSEROLE CONTAINS: EGG, MILK PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1135-2024·2024-04-17

    Caramel Apple Pie Recalled for Missing Sub-Ingredient Labels

    Robeson Enterprises is recalling 2,984 units of Pies & Sides Connie's Caramel Apple Pie due to incomplete ingredient labeling. The product labels do not list sub-ingredients for prepared components.

    Product
    PIES & SIDES CONNIE'S CARAMEL APPLE PIE 11 oz INGREDIENTS: APPLE PIE FILLING, SUGARS, VANILLA, CARAMEL EXTRACT BLEACHED FLOUR, SPICES, CONTAINS: WHEAT, PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1145-2024·2024-04-17

    Robeson Enterprises Recalls Strawberry Pie for Missing Sub-Ingredient Labeling

    Robeson Enterprises is recalling Pies & Sides Strawberry Pie because the label fails to list sub-ingredients. Consumers with allergies cannot verify safe ingredients. The recall affects Georgia, North Carolina, and South Carolina.

    Product
    PIES & SIDES STRAWBERRY PIE INGREDIENTS: STRAWBERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1134-2024·2024-04-17

    Cherry Pie Recalled for Missing Sub-Ingredient Label Information

    Robeson Enterprises is recalling cherry pie products because labels do not list sub-ingredients. Products were distributed in Georgia, North Carolina, and South Carolina.

    Product
    PIES & SIDES CHERRY PIE INGREDIENTS: CHERRY PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR SPICES. CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Drugs)·D-0438-2024·2024-04-17

    FDA Recalls Lansoprazole Delayed-Release Capsules for Manufacturing Practice Deviations

    NATCO Pharma Limited is voluntarily recalling 30 bottles of Lansoprazole 15 mg delayed-release capsules due to Current Good Manufacturing Practice deviations. The product was distributed nationwide in the United States.

    Product
    Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1141-2024·2024-04-17

    Peach pie recalled for missing sub-ingredient information

    Robeson Enterprises is recalling Peach Pie distributed to GA, NC, and SC because the label fails to list sub-ingredients. The recall affects all lots shipped before February 23, 2024.

    Product
    PIES & SIDES PEACH PIE INGREDIENTS: PEACH PIE FILLING, SUGARS, VANILLA, BLEACHED FLOUR, SPICES, CONTAINS: WHEAT PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • ModerateFDA (Food)·F-1137-2024·2024-04-17

    Green Bean Casserole Missing Ingredient Label for Common Allergens

    Green Bean Casserole recalled by Robeson Enterprises due to missing ingredient labels. Product contains undeclared milk, soy, fish, and wheat allergens.

    Product
    PIES & SIDES GREEN BEAN CASSEROLE, CONTAINS: MILK, SOY, FISH, WHEAT, PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • LowFDA (Food)·F-1142-2024·2024-04-17

    Potato Bake Recalled for Failure to List Sub-Ingredients

    Robeson Enterprises is recalling PIES & SIDES DOT'S POTATO BAKE due to incomplete ingredient labeling. The label fails to list sub-ingredients.

    Product
    PIES & SIDES DOT'S POTATO BAKE 2lb INGREDIENTS: IDAHO POTATOES, MONT JACK, CHEDDAR, SHARP CHEEDAR, & CREAM CHEESES. SOUR CREAM, CHICKEN BROTH, BUTTER, CHIVES, SPICES. CONTAINS: MILK, SOY, FISH PIES & SIDES MOUNT HOLLY, NC
    Category
    Food
    Distribution
    3 states
  • SevereNHTSA·24V270000·2024-04-16

    Kawasaki Recalls 2024 Z900RS Motorcycles Due to Front Tire Defect

    Kawasaki is recalling 2024 Z900RS motorcycles because a manufacturing error may cause front tire blistering, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI ZR900C, ZR900E, ZR900N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V271000·2024-04-16

    2023 Kia Niro EV Differential Bolt Recall: Loss of Drive Power Risk

    Kia is recalling certain 2023 Niro EV vehicles because differential gear bolts may not be properly tightened, potentially causing loss of drive power or differential lock-up, which can increase crash risk.

    Product
    KIA — KIA NIRO EV, EV9
    Category
    Vehicle
    Distribution
    Distributed nationwide