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.

37201–37225 of 80118

  • LowFDA (Devices)·Z-1198-2019·2019-04-24

    Cordis Guiding Catheters Recalled for Frayed Mounting Card Fragments

    Cordis Corporation is recalling Vista Brite Tip and Androit guiding catheters because frayed pieces of the mounting card were found inside the primary packaging.

    Product
    Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1132-2019·2019-04-24

    Estee Lauder Recalls Repairwear Cream Due to Ineffective Container Seal

    Estee Lauder Inc is recalling 14,490 jars of Repairwear Laser Focus Line Smoothing Cream SPF 15 because the seal between the cap and jar is ineffective.

    Product
    Repairwear Laser Focus Line Smoothing Cream Broad Spectrum SPF 15, packaged in a light green folding carton containing a 50 mL silver jar with a silver cap, Clinique Laboratories, Dist. New York, NY 10022
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V319000·2019-04-23

    Toyota Recalls 2015-2017 Yaris Vehicles for Air Bag Wire Harness Defect

    Toyota is recalling 2015-2017 Yaris vehicles because wire harnesses for side air bag sensors may crack and corrode, potentially causing air bags to fail to deploy or deploy improperly.

    Product
    TOYOTA — TOYOTA YARIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V318000·2019-04-23

    Toyota Recalls 2019 Sienna Vehicles Due to Passenger Air Bag Sensor Defect

    Toyota is recalling 2019 Sienna vehicles because incorrect welds in the passenger front door may affect air bag sensor readings, potentially causing unintended deployment or failure to deploy.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V320000·2019-04-23

    Jeep Wrangler Recall for Roof Top Tent Cover Detachment Risk

    American Fastbacks is recalling 2018 Jeep Wranglers with roof top tents because the cover may crack and detach while driving, creating a road hazard.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19T004000·2019-04-22

    Toyo Recalls Proxes A27 Tires Due to Tread Detachment Risk

    Toyo is recalling specific Proxes A27 tires where a rubber compound error may cause tread to detach, increasing crash risk.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V317000·2019-04-19

    Forest River Recalls 2019 Rockwood and Flagstaff Trailers for Fire Risk

    Forest River is recalling 2019 Rockwood and Flagstaff recreational trailers because improperly installed air conditioning wiring may contact a heat strip, increasing the risk of fire.

    Product
    FOREST RIVER — FOREST RIVER FLAGSTAFF, ROCKWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V315000·2019-04-18

    Honda Recalls 2017-2018 Clarity Fuel Cell Vehicles for Water Pump Defect

    Honda is recalling 2017-2018 Clarity Fuel Cell vehicles because internal corrosion may cause the water pump to fail, potentially leading to a vehicle stall and increased crash risk.

    Product
    HONDA — HONDA CLARITY FUEL CELL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V314000·2019-04-18

    Mercedes-Benz Recalls 2019 A 220 Vehicles Due to Brake Pedal Welding Defect

    Mercedes-Benz is recalling 2019 A 220 and A 220 4MATIC vehicles because improper welding may cause the pedal plate to bend, impairing brake pedal operation and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ A 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E030000·2019-04-18

    Bendix Recalls Air Disc Brake Calipers for School Buses

    Bendix is recalling ADB22X Air Disc Brake Calipers for school buses because the driver side rear brakes may drag, increasing the risk of fire.

    Product
    SERVICE BRAKES, AIR:DISC recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19107·2019-04-18

    Tekno Recalls Tuff Smoke-Less Grills Due to Fire and Burn Hazards

    Tekno Products is recalling Tuff smoke-less grills because they can overheat, posing fire and burn hazards. Consumers should stop using the grills and return them for a refund.

    Product
    Tuff smoke-less grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V312000·2019-04-18

    GM Recalls 2017-2019 Chevrolet Trax for Front Suspension Weld Defect

    General Motors is recalling 2017-2019 Chevrolet Trax vehicles because improperly welded front lower-control arm joints may break, causing partial separation and increased crash risk.

    Product
    CHEVROLET — CHEVROLET TRAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V309000·2019-04-18

    2019 Mercedes-Benz Sprinter Recalled for High-Beam Software Error

    Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vans because a software error may prevent drivers from turning off high beams, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V316000·2019-04-18

    Nissan Recalls 2019 Altima Vehicles Due to Fuel Pump Lock Ring Defect

    Nissan is recalling 2019 Altima vehicles with front-wheel drive and 2.5-liter engines because a fuel pump lock ring may not be fully engaged, potentially causing a fuel leak and fire risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19108·2019-04-18

    Target Recalls Wooden Toy Vehicles Due to Choking Hazard

    Target is recalling Bullseye's Playground wooden toy vehicles because wheels can detach, posing a choking hazard to children.

    Product
    Bullseye's Playground wooden toy vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19739·2019-04-18

    RH Recalls Callum Canopy Beds Due to Falling Rail Injury Hazard

    RH is recalling Callum Canopy Beds because horizontal canopy rails can detach and fall. No injuries have been reported, but consumers should stop using the beds until repaired.

    Product
    Callum Canopy Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V313000·2019-04-18

    MobilityTrans Recalls Modified Ford and Ram Vans with Defective Foldaway Seats

    Mobility Transportation Services is recalling modified Ford and Ram vans because foldaway seats may not stay locked during a crash, increasing injury risk.

    Product
    FORD — FORD, RAM, MOBILITY SPECIALISTS E-350, E-250, PROMASTER, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1135-2019·2019-04-17

    FDA Recalls Leopard Miracle Honey Containing Undeclared Sildenafil

    USA LESS Inc. is recalling Leopard Miracle Honey because it contains undeclared sildenafil, an unapproved drug for erectile dysfunction.

    Product
    LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1 Sachet 15 gr / 0.53 Oz is labeled as LEOPARD Miracle of Honey, UPC 8 699415 912859, Manufactured in Turkey, www leopardhoneytr.com.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1300-2019·2019-04-17

    Theo Chocolate Sea Salt 70% Dark Chocolate Bars Recalled for Undeclared Milk

    Theo Chocolate is recalling Sea Salt 70% Dark Chocolate bars due to undeclared milk. The product was distributed nationwide.

    Product
    Sea Salt 70% Dark Chocolate 3 oz. bars, wrapped in foil and paper wrapper, brand Theo Chocolate, UPC 8 74492 00325 8. The Sea Salt 70% Dark Chocolate 3 oz. bar's label is read in part: "***Sea Salt 70% Dark Chocolate *** Ingredients: Cocoa Beans, Cane Sugar, Sea Salt, Ground…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1118-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA testing found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 100mg/12.5mg, a) 30-count (NDC: 13668-117-30), b) 90-count (NDC: 13668-117-90) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For: Torrent Pharma, Inc, 150 Allen…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1123-2019·2019-04-17

    Encore Medical Recalls Exprt Precision System Hip Implant Components

    Encore Medical is recalling 22 units of Exprt Precision System hip implant components due to loose or improperly seated bolts that may cause pain or require revision surgery.

    Product
    Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF: 495-00-065, 495-00-075, 495-00-085, 495-01-065, 495-01-075, 495-01-085
    Category
    Medical Device
    Distribution
    26 states
  • SevereFDA (Drugs)·D-1117-2019·2019-04-17

    Torrent Pharma Recalls Losartan Potassium and Hydrochlorothiazide Tablets Due to Impurity

    Torrent Pharma Inc. is recalling Losartan Potassium / Hydrochlorothiazide Tablets because FDA labs found an impurity above acceptable levels.

    Product
    Losartan Potassium / Hydrochlorothiazide Tablets, USP 50mg/12.5mg, a) 30-count (NDC: 13668-116-30), b) 90-count (NDC: 13668-116-90), c) 1000-count (NDC: 13668-116-10) per bottle , Rx only, Manufactured by: Torrent Pharmaceuticals LTD, Indrad-382 721, Dist. Mehsana India. For…
    Category
    Drug
    Distribution
    Distributed nationwide