The Recall Desk

State

Alabama product recalls

73,741 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,377
Critical
1,129
Severe
1,604
Most recent
2026-10-28

Of the 6,377 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 1,604 (25%) are Severe.

Which agencies issued them

These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38826–38850 of 80118

  • HighFDA (Devices)·Z-0585-2019·2018-12-19

    GE Healthcare Recalls B20i Patient Monitors Due to Network Overload Restart Risk

    GE Healthcare is recalling 6,458 B20i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.

    Product
    B20i Patient Monitor and B20i V2 Patient Monitor. The device is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a hospital environment and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0582-2019·2018-12-19

    Medtronic HeartWare HVAD Battery Charger Recalled for Incorrect Inductors

    Heartware, Inc. is recalling 2,031 HVAD System Battery Charger units because they were manufactured with incorrect inductors. The recall covers units distributed in the US and multiple international countries.

    Product
    Medtronic HeartWare Ventricular Assist HVAD System Battery Charger Model 1600US - Product Usage: The HeartWare Ventricular Assist System (HVAD) is indicated in the United States (US) and European Union (EU) for use as a bridge to cardiac transplantation (BTT) as well as an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0703-2019·2018-12-19

    Schwan's Sea Salt Caramel Cashew Ice Cream Recalled for Glass Contamination

    Schwan's is recalling Sea Salt Caramel Cashew Ice Cream due to potential glass contamination. Consumers should check production codes and stop using the product.

    Product
    Schwan's Sea Salt Carmel Cashew Ice Cream (#206). Net Wt 56 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0586-2019·2018-12-19

    GE Healthcare Recalls B40i Patient Monitors Due to Network Restart Risk

    GE Healthcare is recalling 6,864 B40i patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.

    Product
    B40i Patient Monitor and B40i Patient Monitor V3 The device is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a hospital environment and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0605-2019·2018-12-19

    Howmedica Recalls Tritanium Posterior Lumbar Cage Implants Due to Fracture Risk

    Howmedica Osteonics Corp. is recalling 28,461 Tritanium Posterior Lumbar cage implants because of reports of fractures occurring during or after surgery.

    Product
    Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant. Intended for an open, less invasive, and minimally invasive PLIF or TLIF surgical procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V895000·2018-12-19

    Dennis Eagle Elite Refuse Trucks Recalled for Reverse Alarm Mute Switch

    Dennis Eagle is recalling 2017-2018 Elite refuse trucks because the reverse alarm mute switch can prevent the vehicle from beeping in reverse, increasing injury risk.

    Product
    DENNIS EAGLE — DENNIS EAGLE ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0584-2019·2018-12-19

    GE Healthcare Recalls PROCARE B40 Patient Monitors Due to Network Overload Risk

    GE Healthcare is recalling 33,065 PROCARE B40 patient monitors because network configuration issues may cause the devices to restart unexpectedly.

    Product
    PROCARE B40 Patient Monitor, V1; and B40 Patient Monitor, V2, V2.1, and V3. The PROCARE Monitor B40 is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0700-2019·2018-12-19

    Imperial Taste Fried Red Onion Recalled for Undeclared Wheat

    Gemini Food Corporation is recalling Imperial Taste Fried Red Onion because an investigation found undeclared wheat in the ingredients.

    Product
    Imperial Taste Fried Red Onion, Cu Hanh Phi; 24 x 8oz. Item #1760, UPC Code: 741861017607; 24 x 12oz. Item #1761, UPC Code: 741861017614; Ingredients: Red Onion, Palm Oil Product of Vietnam Distributed by Gemini Food Corporation, City Of Inductry, CA 91789
    Category
    Food
    Distribution
    34 states
  • HighNHTSA·18V908000·2018-12-19

    Mercedes-Benz Recalls 2018 S-Class Vehicles for Steering Assist Defect

    Mercedes-Benz is recalling 2018 S-Class and AMG S63 vehicles because an incorrect steering boot installation may keep the Active Steering Assist system engaged while the driver's hands are off the wheel.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S560, S 560 4MATIC, AMG S63, S 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V906000·2018-12-19

    Mercedes-Benz Recalls 2018 C300 Models for Headlight Adjustment Defect

    Mercedes-Benz is recalling 2,364 2018 C300 and C300 4MATIC vehicles because improperly adjusted headlights may reduce driver visibility and increase crash risk.

    Product
    MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C 300 4MATIC, C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0701-2019·2018-12-19

    Fried Garlic Recalled for Undeclared Wheat Ingredient

    Gemini Food Corporation is recalling Imperial Taste Fried Garlic due to undeclared wheat. The product is distributed in multiple states.

    Product
    Imperial Taste Fried Garlic, Tu Phi; 24 x 8oz. Item #1763 UPC Code: 741861017638; 24 x 12oz. Item #1762 UPC Code: 741861017621 Ingredient: Garlic, Palm Oil Product of Vietnam Distributed by Gemini Food Corporation, City of Industry, CA
    Category
    Food
    Distribution
    34 states
  • HighNHTSA·18V911000·2018-12-19

    Mercedes-Benz Recalls 2019 CLS Models for Headlight Adjustment Defect

    Mercedes-Benz is recalling 2019 CLS 450 and AMG CLS53 vehicles because unsealed headlight adjustment screws may cause improper alignment, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450, AMG CLS53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0583-2019·2018-12-19

    GE Healthcare Recalls PROCARE B20 Patient Monitors Due to Network Issues

    GE Healthcare is recalling 28,004 PROCARE B20 patient monitors because network configuration issues may cause the devices to restart unexpectedly.

    Product
    PROCARE B20 Patient Monitor, V1; and B20 Patient Monitor, V2. The PROCARE Monitor B20 is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0587-2019·2018-12-19

    GE Healthcare Recalls B105/125 Patient Monitors Due to Network Overload Risk

    GE Healthcare is recalling 5,516 B105/125 patient monitors worldwide because network configuration issues may cause the devices to restart unexpectedly.

    Product
    B105/125 Patient Monitor. The device is a portable multiparameter unit to be used for monitoring and recording of, and to generate alarms for, multiple physiological parameters of adult, pediatric, and neonatal patients in a hospital environment and during intra-hospital…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0603-2019·2018-12-19

    Philips Recalls HeartStart MRx Lithium-Ion Batteries Due to Defective Component

    Philips is recalling 1,880 HeartStart MRx lithium-ion batteries because a defective component may prevent the battery from charging or delivering power to the monitor/defibrillator.

    Product
    HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx Monitor/Defibrillators.
    Category
    Medical Device
    Distribution
    32 states
  • HighCPSC·19055·2018-12-19

    GNC Recalls Women's Iron Complete Supplements Due to Packaging Defect

    GNC is recalling Women's Iron Complete supplements because the blister packaging is not child-resistant, posing a risk of poisoning to children.

    Product
    Women's Iron Complete Dietary Supplement (60 caplets)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0593-2019·2018-12-19

    St. Jude Medical DBS Leads Recalled for Incorrect Electrode Material

    St. Jude Medical is recalling Deep Brain Stimulation leads where the most proximal unsegmented electrode may be made of MP35N instead of the required 90/10 platinum-iridium.

    Product
    St. Jude Medical InfinityTM DBS System 8CH Directional Lead, 30 cm, 0.5 REF 6170 - STERILE EO Rx ONLY CE 0086 0123 St. Jude Medical Plano, TX St. Jude Medical InfinityTM DBS System 8CH Directional Lead, 40 cm, 0.5 REF 6172 STERILE EO Rx ONLY St. Jude Medical Plano, TX…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0704-2019·2018-12-19

    4Patriots Chicken a la King Recalled for Undeclared Milk Allergen

    4Patriots, LLC is recalling Chicken a la King pouches because milk is not declared on the label. The product was sold nationwide in emergency kits.

    Product
    4Patriots Chicken a la King CONTAINS: Wheat, Coconut NET WT. 10.0 oz (284 g)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0588-2019·2018-12-19

    GE LOGIQ E10 Ultrasound System Recalled for Potential Burn Injury

    GE Healthcare is recalling 103 LOGIQ E10 Ultrasound Systems because a trans-esophageal probe may overheat, posing a risk of burn injury to patients.

    Product
    GE LOGIQ E10 Ultrasound System, Model #530000E10. The device is intended for use by a qualified physician for ultrasound evaluation of Fetal/Obstetrics; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V897000·2018-12-19

    Seagrave Recalls 2017-2018 Emergency Vehicles for Brake Light Defect

    Seagrave is recalling 2017-2018 Capital and Marauder II emergency vehicles because Whelen accessory brake lights may falsely illuminate, increasing crash risk.

    Product
    SEAGRAVE — SEAGRAVE CAPITAL, MARAUDER II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0290-2019·2018-12-19

    CAO Group Recalls fas.TRACT Hemostatic Gel Due to cGMP Violations

    CAO Group, Inc. is recalling fas.TRACT Coagulative Hemostatic Gel kits due to current Good Manufacturing Practice (cGMP) violations identified during a recent inspection.

    Product
    fas.TRACT Coagulative Hemostatic Gel, 10% Ferric Sulfate Kit, Rx Only, (3) 3cc Preloaded Syringes/ (50) Scrub Tips. Distributed by: Benco Dental, 295 Center Point Blvd., Pittston, PA 18640. NDC: 14060-01105
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0600-2019·2018-12-19

    Tosoh AIA-900 and AIA-2000 Analyzers Recalled for Incubator Slippage Risk

    Tosoh Bioscience is recalling AIA-900 and AIA-2000 analyzers due to a potential incubator slippage issue that may cause system errors and delays in patient test results.

    Product
    AIA-900Analyzer, Product code 022930, 022930R The AIA-2000 analyzer and AIA-900 analyzer are capable of performing three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric…
    Category
    Medical Device
    Distribution
    Distributed nationwide