The Recall Desk

State

Georgia product recalls

73,738 recalls have nationwide distribution and so reach Georgia. 9,632 additional recalls listed Georgia specifically in their distribution scope.

What the numbers show

Total
9,632
Critical
1,471
Severe
2,565
Most recent
2026-10-28

Of the 9,632 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 2,565 (27%) are Severe.

These figures cover only the 9,632 recalls whose distribution notice names Georgia specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35626–35650 of 83370

  • HighNHTSA·19V793000·2019-11-05

    McElrath Trailers Recalls 2014-2019 VX Models for Missing Reflectors

    McElrath Trailers is recalling 2014-2019 VX trailers because side marker LED lights may lack required reflex reflectors, reducing visibility.

    Product
    MCELRATH TRAILERS — MCELRATH TRAILERS VX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V794000·2019-11-05

    KZRV Recalls 2019-2020 Trailers With Detaching Rear Storage Racks

    KZRV is recalling 2019-2020 Connect and Sportsmen trailers because optional Rock Run rear storage racks may detach when loaded, creating a road hazard.

    Product
    KZRV — KZRV CONNECT, SPORTSMEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V792000·2019-11-04

    Daimler Recalls Western Star Trucks for Detaching Vent Windows

    Daimler Trucks is recalling 2,725 Western Star 4900 and 5700 trucks because sleeper cab vent windows may detach due to improper adhesive.

    Product
    WESTERN STAR — WESTERN STAR 5700, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V787000·2019-11-01

    Mercedes-Benz Recalls Vehicles for Emergency Call System Software Fault

    Mercedes-Benz is recalling 24,226 vehicles due to a software fault that may cause the emergency call system to relay inaccurate location data, potentially delaying emergency responders.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ B 250E, AMG GL63, SL63, SL550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V788000·2019-11-01

    Mercedes-Benz Recalls Vehicles for Seat Belt Sensor Defect

    Mercedes-Benz is recalling 29,720 vehicles because front seat belts may be incorrectly detected as unfastened, potentially disabling safety features.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450, E 300, AMG GT63, E 400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·19V782000·2019-10-31

    Mazda Recalls CX-7, CX-9, and Mazda6 for Air Bag Inflator Defect

    Mazda is recalling specific 2007-2012 CX-7, CX-9, and 2009-2012 Mazda6 vehicles because the front passenger air bag inflators may explode, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA CX-7, CX-9, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V783000·2019-10-31

    Gulf Stream Recalls 2020 Trailers Due to Gas Refrigerator Seal Defect

    Gulf Stream is recalling 2020 Amerilite, Conquest, Innsbruck, Grand River, Kingsport, and Trail Master trailers because the gas refrigerator may not be properly sealed, potentially releasing carbon monoxide or flammable LP gases.

    Product
    GULF STREAM — GULF STREAM INNSBRUCK, KINGSPORT, CONQUEST, TRAILMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V784000·2019-10-31

    Honda Recalls Pilot and Passport for Incomplete Body Welding

    Honda is recalling 2019-2020 Pilot and 2019 Passport vehicles because front frame members may not be fully welded, potentially reducing crash protection.

    Product
    HONDA — HONDA PILOT, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V781000·2019-10-31

    Mazda Recalls Vehicles Due to Front Passenger Air Bag Inflator Defect

    Mazda is recalling specific 2003-2008 models because front passenger air bag inflators may explode, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA MAZDA6, MPV, RX-8, MAZDASPEED6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20706·2019-10-31

    John Deere Recalls Compact Utility Tractors Due to Cab Bolt Failure Hazard

    John Deere is recalling 4044R, 4052R, and 4066R compact utility tractors because improperly torqued front cab support bolts can fail during a rollover, posing a crushing injury hazard.

    Product
    John Deere 4044R, 4052R and 4066R compact utility tractors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0057-2020·2019-10-30

    Roland Black Caviar Recalled for Potential Botulism Contamination

    Roland Foods is recalling specific jars of Black Caviar due to potential Clostridium botulinum contamination. Consumers should check their pantries for the listed UPCs and batch codes.

    Product
    Roland Brand Black Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224200029; 3.5oz, UPC: 41224200203; 12oz, UPCs: 41224200401 & 41224200425
    Category
    Food
    Distribution
    27 states
  • CriticalFDA (Food)·F-0063-2020·2019-10-30

    Mrs. Stratton's Salads Recalls Tuna Salad for Listeria Risk

    Mrs. Stratton's Salads is recalling 27,787 containers of tuna salad under four brand names due to potential Listeria monocytogenes contamination.

    Product
    Tuna salad under the following brand names: BALLARDS FARM Barboursville, WV 25504 UPC 076010000293 12 oz. plastic container, LAURA LYNN UPC 086854035368 12 oz. plastic container, MRS. STRATTON S SALADS Birmingham, AL 35219 UPC 075217100294 12 oz. plastic container, STAR FOOD…
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-0058-2020·2019-10-30

    Roland Brand Red Caviar Recalled for Potential Botulism Contamination

    Roland Foods is recalling specific jars of Red Caviar due to potential Clostridium botulinum contamination. Consumers should check their pantries for the listed UPCs and batch codes.

    Product
    Roland Brand Red Caviar - Whole Grain Lumpfish (Lumpfish Roe) packed in glass jars - 2oz & 2x2oz, UPC: 41224202023; 3.5oz, UPC: 41224202207; 12oz, UPCs: 41224202405 & 41224202420
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0187-2020·2019-10-30

    Torrent Suite Dx Software Recalled for Incorrect Positive Variant Results

    Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for clinical variants.

    Product
    Torrent Suite Dx Software Version 5.6.4 Catalog Number:A33178 OEM Customer software: Sentosa SQ Suite Software v5.6.20 UDI: (01)10190302005654 (11)000000 (10)5.6.4 (240)A33178
    Category
    Medical Device
    Distribution
    17 states
  • SevereFDA (Drugs)·D-0152-2020·2019-10-30

    Avella Recalls Povidone Iodine Ophthalmic Solution Due to Sterility Concerns

    Avella of Deer Valley, Inc. is recalling 808 droptainers of Povidone Iodine, 5% Ophthalmic Solution due to a lack of sterility assurance.

    Product
    Povidone Iodine, 5% Ophthalmic Solution, 5 mL per droptainer, Repackaged by: Avella Specialty Pharmacy, 24416 N. 19th Ave., Phoenix, AZ 85085. NDC 42852-006-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0150-2020·2019-10-30

    Nephron Amino Acid Injection Recalled for Sterility and Leak Concerns

    Nephron Pharmaceuticals is recalling 162 bags of Amino Acid Injection due to lack of sterility assurance and potential leaks.

    Product
    Amino Acid Injection 50 g/1000 mL (50 mg/mL) 25 g L-Arginine HCl; 25 g L-Lysine HCl, Single Dose Container, Rx Only Nephron 503B outsourcing facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-988-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0185-2020·2019-10-30

    Life Technologies Recalls Torrent Suite Dx Software for Incorrect Results

    Life Technologies is recalling Torrent Suite Dx software because it may incorrectly display positive results for specific clinical variants.

    Product
    Torrent Suite Dx Software Version (IUO) 5.2 Catalog Number: A29225 OEM Customer Software: Sentosa SQ Suite Software v5.6.9
    Category
    Medical Device
    Distribution
    17 states
  • SevereFDA (Drugs)·D-0151-2020·2019-10-30

    Nephron Recalls del Nido Cardioplegia Solution Due to Sterility Concerns

    Nephron Pharmaceuticals is recalling 1,047 bags of del Nido Cardioplegia Solution because the bags may leak, compromising sterility.

    Product
    del Nido Cardioplegia Solution, 1000 mL, Single-Dose Container, Rx Only Nephron 503B Outsourcing Facility 4500 12th St. Extension West Columbia, SC 29172 NDC: 69374-984-10
    Category
    Drug
    Distribution
    Distributed nationwide