The Recall Desk

State

Alabama product recalls

73,806 recalls have nationwide distribution and so reach Alabama. 6,378 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,378
Critical
1,129
Severe
1,605
Most recent
2026-11-04

Of the 6,378 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,605 (25%) are Severe.

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41276–41300 of 80184

  • SevereNHTSA·18E057000·2018-07-18

    Brembo Recalls Federal Mogul Rear Brake Pads Due to Material Detachment

    Brembo is recalling certain Federal Mogul rear brake pads because the material may detach from the back plate, potentially affecting braking performance.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:PADS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V479000·2018-07-18

    Freightliner Recalls 2019 Cascadia Trucks for Tire Defect

    Daimler Trucks North America is recalling 2019 Freightliner Cascadia trucks equipped with specific Continental tires that may lose air suddenly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2397-2018·2018-07-18

    Stryker Recalls Specific Femoral Nail Due to Potential Breakage Risk

    Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.

    Product
    Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-1011-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling White Borneo Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Borneo, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2417-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 8,890 EnTrust ICDs due to a potential loss of high voltage therapy near end-of-life. Patients should contact their healthcare provider.

    Product
    Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154ATG Product Usage: The device indicated for use in ICD patients with atrial tachyarrhythmias, or who are at significant risk of developing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2406-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, RIGHT T2 GTN ¿14x460 mm, Product Number 18511446S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2418-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 3 EnTrust ICDs because they may lose high voltage therapy near battery end-of-life without prior warning.

    Product
    Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D153VRC Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2393-2018·2018-07-18

    Stryker Tibial Nail Recall Due to Potential Premature Breakage

    Stryker GmbH is recalling specific Tibial Nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Tibial Nail, Standard T2 Tibia ¿12x315 mm, Product Number 18221231S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2420-2018·2018-07-18

    Medtronic EnTrust Escudo ICD Recall for Potential Loss of Therapy

    Medtronic is recalling EnTrust Escudo ICDs due to a potential loss of high voltage and anti-tachycardia pacing therapy as the battery nears its end of life.

    Product
    Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V475000·2018-07-18

    Forest River Recalls 2018-2019 Trailers Due to Wheel Bearing Defect

    Forest River is recalling 2018-2019 Rockwood and Flagstaff trailers because inner wheel bearings may seize, causing wheels to lock up and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2405-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.

    Product
    Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2395-2018·2018-07-18

    Stryker Recalls 17 Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling 17 femoral nails because non-conforming cannulation may reduce component strength and cause premature breakage.

    Product
    Femoral Nail, A/R T2 Femur ¿10x340 mm, Product Number 18251034S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-1014-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling White Thai Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, White Thai, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2408-2018·2018-07-18

    Stryker Recalls Ankle Arthrodesis Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Ankle Arthrodesis Nail, right T2 Ankle ¿11x300mm, Product Number 18191130S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2401-2018·2018-07-18

    Stryker Recalls Specific Femoral Nail Products Due to Potential Breakage

    Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿12x380 mm, Product Number 18281238S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Drugs)·D-1030-2018·2018-07-18

    AuroMedics Recalls Piperacillin and Tazobactam Injection Vials Due to Particulate Matter

    AuroMedics Pharma LLC is recalling 73,620 vials of Piperacillin and Tazobactam for Injection due to the presence of glass and silicone particulate matter.

    Product
    PIPERACILLIN AND TAZOBACTAM — PIPERACILLIN AND TAZOBACTAM (PIPERACILLIN SODIUM AND TAZOBACTAM SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0994-2018·2018-07-18

    Gaia Kratom Powder Recalled for Salmonella Contamination

    Gaia Ethnobotanical LLC is recalling specific lots of Gaia Kratom powder due to FDA-confirmed Salmonella contamination.

    Product
    Gaia Kratom (mitragyna speciosa) powder, Elephant, 1oz, 250g, 1kg packages, Gaia Ethnobotanical.com
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2394-2018·2018-07-18

    Stryker Recalls Two Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling two femoral nails that may have non-conforming cannulation, potentially leading to reduced strength and premature breakage.

    Product
    Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2419-2018·2018-07-18

    Medtronic EnTrust ICD Recall for Potential Loss of High Voltage Therapy

    Medtronic is recalling 8,821 EnTrust ICDs due to a potential loss of high voltage therapy near end-of-life. Patients should contact their healthcare provider.

    Product
    Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with Atrial and Ventricular Therapies and RapidRead Telemetry, D154VRC Product Usage: The implantable cardioverter defibrillator is intended to provide ventricular antitachycardia pacing and ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2404-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, LEFT T2 GTN ¿14x300 mm, Product Number 18501430S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2398-2018·2018-07-18

    Stryker Recalls Seven Femoral Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling seven femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2400-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿12x360 mm, Product Number 18281236S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2407-2018·2018-07-18

    Stryker Recalls Ankle Arthrodesis Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2399-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿12x300 mm, Product Number 18281230S
    Category
    Medical Device
    Distribution
    8 states