The Recall Desk

State

Alabama product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

31926–31950 of 80111

  • ModerateFDA (Devices)·Z-1552-2020·2020-04-01

    Quidel Triage TOX Drug Screen Control 1 Kit Recall for Chip Error

    Quidel is recalling Triage TOX Drug Screen Control 1 kits due to a programming error in the control chip that causes false failing results for AMP and mAMP tests.

    Product
    Quidel Triage TOX Drug Screen Control 1 Kit Box containing 5 Control 1 vials with 5 x 0.25 mL vials per box. Quidel Cardiovascular Inc. 9975 Summers Ridge Road San Diego, CA 92121 USA Quidel.com
    Category
    Medical Device
    Distribution
    19 states
  • ModerateFDA (Food)·F-0893-2020·2020-04-01

    Alkamind Creamy Chocolate Protein Recalled for Unapproved Herbicide

    Organic By Nature, Inc. is recalling Alkamind Creamy Chocolate Organic Daily Protein due to the presence of unapproved herbicide Haloxyfop in the flaxseed powder ingredient.

    Product
    Alkamind Creamy Chocolate Organic Daily Protein; 450g Plastic Bottle; Finished Product Item # FAMCDP450G; 3 core alkaline proteins Distributed by Alkamind LLC, New York, NY 10028
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1570-2020·2020-04-01

    Bard PowerPort Implantable Ports Recalled Due to Incorrect Catheter Barb Tip

    Bard Peripheral Vascular Inc is recalling 178 PowerPort implantable ports because they may contain a tunneler with an incorrect barb tip, potentially prolonging surgery.

    Product
    1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen Venous Catheter REF: 1709600, Air Guard, With suture Plugs, (01)00801741026720; 2. PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single- Lumen Venous Catheter, REF: 1709601, Air Guard…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0899-2020·2020-04-01

    Purim Daily Fiber Blend Recalled for Unapproved Herbicide Contamination

    Organic By Nature, Inc. is recalling Purim Daily Fiber Blend because the flaxseed ingredient contains unapproved herbicide Haloxyfop.

    Product
    Purim Daily Fiber Blend - Original unflavored; 540g Plastic Bottle, 180g Plastic Bottle; Finished Product Item#: 2014, 2014-P65, 2015, 2015-P65 Purim - Rancho Dominguez, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1049-2020·2020-04-01

    FDA Recalls Colostat Homeopathic Remedy Due to Incorrect Labeling

    Grato Holdings, Inc. is recalling 659 bottles of Colostat homeopathic remedy because the indications on the product label are incorrect.

    Product
    COLOSTAT — COLOSTAT (RHAMNUS PURSHIANA, SPIGELIA ANTHELMIA, TARAXACUM OFFICINALE, CAJUPUTUM, HYDRASTIS CANADENSIS, ALUMINA, CINA, CINCHONA OFFICINALIS, LYCOPODIUM CLAVATUM, MAGNESIA PHOSPHORICA, MANDRAGORA OFFICINARUM, NUX VOMICA)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E018000·2020-03-31

    Cummins Recalls B6.7 Diesel Engines Due to Fuel Heater Fire Risk

    Cummins is recalling specific B6.7 diesel engines used in school buses, trucks, and emergency vehicles because the fuel heater may overheat, melt, or cause a fire.

    Product
    FUEL SYSTEM, DIESEL: PRE-HEATER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V189000·2020-03-31

    Subaru Recalls 2019 Crosstrek Vehicles for Rear Seat Belt Defect

    Subaru is recalling 2019 Crosstrek vehicles because the rear seat belt locking mechanism may not function as intended, increasing injury risk in crashes.

    Product
    SUBARU — SUBARU CROSSTREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V188000·2020-03-30

    Nissan Recalls NV, Titan, Armada, QX56 for Air Bag Inflator Defect

    Nissan is recalling 216,678 vehicles from 2011-2017 because the driver-side air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    INFINITI — INFINITI, NISSAN QX56, NV, ARMADA, TITAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V186000·2020-03-27

    Can-Am Recalls 2020 Spyder RT Motorcycles Due to Brake Failure Risk

    Bombardier is recalling 2020 Can-Am Spyder RT motorcycles because a brake support could break during emergency braking, causing total loss of braking ability.

    Product
    CAN-AM — CAN-AM SPYDER RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V185000·2020-03-26

    BMW Recalls 328d Vehicles for Driveline Joint Defect

    BMW is recalling 2013-2016 328d xDrive vehicles because a driveline joint may fail, causing loss of rear power and increasing crash risk.

    Product
    BMW — BMW 328D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V183000·2020-03-26

    Chrysler Recalls 2019 Jeep Grand Cherokee and Dodge Durango for Driveline Defect

    Chrysler is recalling 2019 Jeep Grand Cherokee and Dodge Durango vehicles because insufficiently hardened front differential pinion gears can wear down, leading to a loss of power or the PARK function.

    Product
    JEEP — JEEP, DODGE GRAND CHEROKEE, DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E017000·2020-03-26

    Land Rover Recalls 2020 Range Rover Evoque Headliners for Safety Defect

    Land Rover is recalling 2020 Range Rover Evoque vehicles because some headliners lack a required metal plate, potentially reducing head impact protection in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V180000·2020-03-26

    2019 Mercedes-Benz and Freightliner Sprinter Recall for Manual Error

    Daimler Vans USA is recalling 2019 Sprinter vans because the Operator's Manual may contain incorrect information about the automatic parking function, potentially increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V184000·2020-03-26

    GM Recalls 2019-2020 Chevrolet Bolt EV for Rear Door Cable Defect

    General Motors is recalling 2019-2020 Chevrolet Bolt EVs because a rear door cable may be too long, potentially causing the door to open unintentionally while driving.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1499-2020·2020-03-25

    Philips Recalls HeartStart MRx Defibrillators Due to Internal Damage Risk

    Philips is recalling HeartStart MRx Monitor/Defibrillators because internal damage from drops or shocks may prevent therapy delivery, even if the device appears undamaged.

    Product
    HeartStart MRx Monitor/Defibrillators with model numbers M3535A M3536A, M3536M, M3536MC, M3536M2, M3536M3, M3536M4, M3536M5, M3536M6, M3536M7, M3536M8, and M3536M9.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0860-2020·2020-03-25

    Chicago Indoor Garden Recalls Sprout Salad Due to E. coli Outbreak

    Chicago Indoor Garden, Inc. is recalling Sprout Salad 6 oz. because FDA analysis found E. coli and linked the product to an outbreak.

    Product
    Sprout Salad 6 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0861-2020·2020-03-25

    Chicago Indoor Garden Recalls Mixed Greens Contaminated with E. coli

    Chicago Indoor Garden is recalling Mixed Greens containing red clover sprouts because FDA testing found E. coli. The product was distributed nationwide, primarily through Whole Foods.

    Product
    Mixed Greens 4 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0858-2020·2020-03-25

    Chicago Indoor Garden Recalls Red Clover Products Due to E. coli

    Chicago Indoor Garden, Inc. is recalling Red Clover products because FDA analysis found E. coli and linked the firm to an outbreak.

    Product
    Red Clover 4 oz, Red Clover 2 Lbs. Products have Red Clover as an ingredient.
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1036-2020·2020-03-25

    UP2 Libido Supplement Recalled for Undeclared Sildenafil

    Med Man Distribution is recalling UP2 dietary supplements because FDA analysis found undeclared sildenafil, a prescription drug, in the product.

    Product
    UP2, Dietary Supplement, All Natural Libido for Men & Women, a) one pack, b) four pack, c) ten pack capsules per carton, Exclusively Manufactured and Formulated by: Buy Wise Marketing, 4234 I-75 Business Spur, Sault Ste Marie, MI 49783, Ultimatepleasure2.com.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0859-2020·2020-03-25

    Chicago Indoor Garden Recalls Spring Salad Sprouts Due to E. coli

    Chicago Indoor Garden, Inc. is recalling Spring Salad 6 oz. containing red clover sprouts because FDA testing found E. coli and linked the product to an outbreak.

    Product
    Spring Salad 6 oz. Product contains red clover sprouts.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1015-2020·2020-03-25

    Perrigo Recalls Ranitidine Tablets Due to Possible N-Nitrosodimethylamine Contamination

    Perrigo Company PLC is recalling specific lots of Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.

    Product
    Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 150 tablets per bottle. [NDC: Brand] NDC H.E.B.: 37808-876-47; NDC Equate: 49035-876-47
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1474-2020·2020-03-25

    CME America BodyGuard Infusion Pump Systems Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Infusion Pump Systems because they may deliver drugs at inaccurate rates, potentially causing faster or slower than expected medication administration.

    Product
    CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and CMExpress
    Category
    Medical Device
    Distribution
    45 states
  • SevereFDA (Drugs)·D-1012-2020·2020-03-25

    Perrigo Recalls Ranitidine Tablets Due to Potential N-Nitrosodimethylamine Contamination

    Perrigo Company PLC is recalling Regular Strength Acid Reducer (Ranitidine) tablets due to a CGMP deviation and possible contamination with the impurity N-nitrosodimethylamine.

    Product
    Regular Strength Acid Reducer, Ranitidine tablets, USP 75 mg, 30 tablets per bottle. [NDC: Brand] NDC CVS Health: 69842-293-65; NDC Equaline 41163-931-65; NDC Family Wellness: 55319-876-65; NDC Good Sense 0113-0876-65; NDC H.E.B.: 37808-876-65; NDC Harris Teeter: 69256-876-65…
    Category
    Drug
    Distribution
    Distributed nationwide