The Recall Desk

State

Georgia product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57576–57600 of 83468

  • SevereFDA (Devices)·Z-0561-2016·2016-01-06

    Beckman Coulter MicroScan Pos Breakpoint Combo Panel Recall

    Beckman Coulter is recalling MicroScan Pos Breakpoint Combo Panel Type 20 due to falsely negative Voges-Proskauer results.

    Product
    MicroScan Pos Breakpoint Combo Panel Type 20, Part No. B1017-202 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0569-2016·2016-01-06

    BD Vacutainer PLUS K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because they may contain insufficient EDTA additive, which can lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 3.0 mL (Lavender) BD Hemogard Additive: K2EDTA (spray dried), 5.4mg Sterile IVD BD, Made in USA BD Vacutainer¿ tubes are used to collect, transport and process blood in a closed system. These tubes are used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·004-2016·2016-01-06

    Neto's Sausage Recalls Meat and Poultry Products Labeled Without Inspection

    Neto's Sausage Co. is recalling approximately 7,687 pounds of beef, pork, and chicken products that were labeled with the federal mark of inspection without FSIS oversight.

    Product
    Silva Sausage Co. — Neto's Sausage Co., Inc. Recalls Meat and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0568-2016·2016-01-06

    BD Vacutainer PLUS K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 2.0 mL (Pink) BD Hemogard Additive: K2EDTA (spray dried), 3.6mg Sterile IVD BD, Made in USA BD Vacutainer¿ tubes are used to collect, transport and process blood in a closed system. These tubes are used for testing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0570-2016·2016-01-06

    BD Vacutainer PLUS K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 3.0 mL (Tan) BD Hemogard Additive: K2EDTA (spray dried), 5.4mg Sterile IVD BD, Made in USA BD Vacutainer¿ tubes are used to collect, transport and process blood in a closed system. These tubes are used for testing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0559-2016·2016-01-06

    Beckman Coulter MicroScan Pos Combo Panel Recall for False Negative Results

    Beckman Coulter is recalling MicroScan Pos Combo panels that may produce falsely negative Voges-Proskauer results for Staphylococcus aureus.

    Product
    MicroScan Pos Combo Panel Type 33, Part No. B1017-211 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0563-2016·2016-01-06

    Trumpf Ceiling Mounted Surgical Light Systems Recalled for Falling Hazard

    Trumpf Medical Systems is recalling 20,713 ceiling-mounted surgical light systems because the spring arm can detach, causing the light head to fall.

    Product
    Ceiling Mounted Surgical Light System TruLight 3000/5000 and Ceiling Mounted Surgical Light System iLED3/iLED5
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0567-2016·2016-01-06

    BD Vacutainer PLUS K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA blood collection tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 2.0 mL (Pink) BD Hemogard Additive: K2EDTA (spray dried), 3.6mg Sterile IVD BD, Made in USA The Vacutainer Brand PLUS (Plastic) Tube with EDTA Vacutainer¿ Brand Serum Tube are evacuated blood collection tubes which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0560-2016·2016-01-06

    Beckman Coulter MicroScan Pos Combo Panels Recalled for False Negative Results

    Beckman Coulter is recalling MicroScan Pos Combo and Breakpoint Combo panels due to falsely negative Voges-Proskauer results with Staphylococcus aureus.

    Product
    MicroScan Pos Combo Panel Type 34, Part No. B1017-214 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0558-2016·2016-01-06

    Beckman Coulter MicroScan Pos Combo Panel Recall for False Negatives

    Beckman Coulter is recalling MicroScan Pos Combo panels due to falsely negative Voges-Proskauer results with Staphylococcus aureus.

    Product
    MicroScan Pos Combo Panel Type 21, Part No. B1017-201 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci, some…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0571-2016·2016-01-06

    BD Vacutainer K2EDTA Tubes Recalled for Insufficient Additive

    Becton Dickinson is recalling specific lots of BD Vacutainer PLUS K2EDTA tubes because some were manufactured with insufficient EDTA additive, which may lead to erroneous platelet results.

    Product
    BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm x 4.0 mL (Lavender) BD Hemogard Additive: K2EDTA (spray dried), 7.2mg Sterile IVD BD, Made in USA BD Vacutainer¿ tubes are used to collect, transport and process blood in a closed system. These tubes are used for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0437-2016·2016-01-06

    Amcane Sugar Recalls Bulk Refined Sugar Due to Foreign Material

    Amcane Sugar LLC is recalling 526,000 lbs of bulk refined sugar because it contains small pieces of brass.

    Product
    Bulk refined sugar. CON AA in 50lb paper bags, 2000 and 2200 poly super totes
    Category
    Food
    Distribution
    4 states
  • ModerateFDA (Devices)·Z-0562-2016·2016-01-06

    Beckman Coulter Recalls MicroScan Pos Breakpoint Combo Panels Due to False Negatives

    Beckman Coulter is recalling MicroScan Pos Breakpoint Combo Panels because they may produce falsely negative results for Staphylococcus aureus quality control tests.

    Product
    MicroScan Pos Breakpoint Combo Panel Type 23, Part No. B1017-206 MicroScan Pos (Positive) panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of rapidly growing aerobic and facultative gram-positive cocci…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0556-2016·2016-01-06

    Biomerieux Recalls Granada Biphasic Broth Due to Missing FDA Clearance

    Biomerieux Inc is recalling 24 cartons of Granada Biphasic Broth because the product lacks required FDA 510(k) clearance for marketing in the United States.

    Product
    Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens.
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Food)·F-0336-2016·2016-01-06

    Friendly Farms Greek Peach Parfait Recalled for Gluten Mislabeling

    Ehrmann Arizona Dairy is recalling Friendly Farms Greek Peach Parfait because the packaging displays a gluten-free logo despite containing wheat flakes.

    Product
    Friendly Farms Greek Peach Parfait Nonfat Yogurt net wt. 5.3 oz (150g) Distributed by ALDI Inc., Batavia, IL 60510
    Category
    Food
    Distribution
    17 states
  • SevereNHTSA·16V002000·2016-01-05

    HME Recalls One 2015 SFO Fire Service Chassis for Axle Defect

    HME is recalling one 2015 SFO fire service chassis because improperly tightened axle nuts could cause the driveshaft to disconnect, increasing crash risk.

    Product
    HME — HME SFO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16719·2016-01-05

    KTM Recalls Competition Off-Road Motorcycles Due to Fuel Hose Fire Hazard

    KTM North America is recalling about 1,800 competition off-road motorcycles because molded fuel hoses could leak fuel, posing a fire hazard. No injuries have been reported.

    Product
    Competition Off-road Motocross Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V003000·2016-01-05

    Foretravel Recalls 2008 Nimbus Motorhomes Due to Unstable Entry Steps

    Foretravel is recalling 2008 Nimbus motorhomes because a bolt on the electric entry steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    FORETRAVEL — FORETRAVEL NIMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V001000·2016-01-04

    AEV Ambulance Wheelchair Van Recall for Lift Bearing Defect

    Halcore is recalling 2006-2013 AEV Ambulance Wheelchair Vans because wheelchair lift bearings may move, causing the platform to fall and injure operators.

    Product
    AEV — AEV AMBULANCE WHEELCHAIR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·001-2016·2016-01-04

    Huisken Meat Company Recalls Beef Patties Due to Wood Contamination

    Huisken Meat Company is recalling Sams Choice Black Angus Beef Patties with Vidalia Onion due to possible wood contamination. No illnesses have been reported.

    Product
    Branding Iron Holdings — Huisken Meat Company Recalls Beef Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V890000·2015-12-31

    Compass Recalls Horse Trailers with Defective Water Heaters

    Compass Conversions is recalling specific 2014 and 2015 horse trailers due to a gas valve defect that may cause water to overheat, posing a scalding risk.

    Product
    PLATINUM — PLATINUM, BLOOMER HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide