The Recall Desk

State

Alabama product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41701–41725 of 80187

  • SevereNHTSA·18V389000·2018-06-11

    Ford Recalls 2018 F-650 and F-750 Trucks for Brake Hose Defect

    Ford is recalling 2018 F-650 and F-750 trucks because brake hose fittings may lack anti-corrosion plating, risking fluid leaks and reduced braking.

    Product
    FORD — FORD F-750 SD, F-650 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V428000·2018-06-11

    BMW Recalls 2000-2006 Models for Passenger Air Bag Inflator Rupture Risk

    BMW is recalling specific 2000-2006 models because the passenger air bag inflator may rupture during deployment, potentially sending metal fragments into the cabin.

    Product
    BMW — BMW 325XI, M3, 330XI, 330I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V386000·2018-06-08

    Forest River Recalls 2019 Salem and Wildwood Trailers for Axle Defect

    Forest River is recalling 2019 Salem and Wildwood recreational trailers because an axle equalizer defect could cause axle failure and increase crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V385000·2018-06-08

    Thor Motor Coach Recalls 2019 Motorhomes Due to Rear Axle Bolt Issue

    Thor Motor Coach is recalling 691 specific 2019 motorhome models because rear axle U-bolts may be insufficiently tightened, posing a risk of axle separation and loss of control.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, OUTLAW, FOUR WINDS, VEGAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V387000·2018-06-08

    Newmar Recalls 2018-2019 Motorhomes Due to Windshield Wiper Defect

    Newmar is recalling 2018-2019 Essex, London Aire, King Aire, and Mountain Aire motorhomes because windshield wiper arms may not contact the glass, reducing visibility.

    Product
    NEWMAR — NEWMAR ESSEX, LONDON AIRE, KING AIRE, MOUNTAIN AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·047-2018·2018-06-08

    Tyson Recalls Breaded Chicken Tenderloins Due to Plastic Contamination

    Tyson Foods is recalling approximately 3,120 pounds of frozen breaded chicken tenderloins that may contain blue or clear soft plastic. The products were shipped to food service establishments nationwide.

    Product
    Tyson Foods Inc. Recalls Breaded Chicken Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V384000·2018-06-07

    Spartan K2 and K3 Motorhome Chassis Recalled for Tire Damage Risk

    Spartan is recalling 2016-2019 K2 and K3 motorhome chassis because the tag axle tire may be damaged by the DEF fill bracket, increasing crash risk.

    Product
    SPARTAN — SPARTAN K3, K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V381000·2018-06-07

    Ferrari Recalls 2012 Models Due to Passenger Air Bag Inflator Defect

    Ferrari is recalling 2012 California, 458, and FF models because the passenger air bag inflator may explode in a crash, potentially causing serious injury or death.

    Product
    FERRARI — FERRARI CALIFORNIA, FF, 458
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V379000·2018-06-07

    Altec Recalls 2016-2017 Aerial Devices and Digger Derricks for Grounding Defect

    Altec is recalling 2016-2017 Aerial Devices and Digger Derricks because improperly sized cable connection receptacles may cause the high voltage grounding system to fail, increasing the risk of injury.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V382000·2018-06-07

    Mobility Ventures Recalls MV-1 Vehicles for Turn Signal Defect

    Mobility Ventures is recalling 2015-2016 MV-1 vehicles because a failed rear turn signal does not alert the driver, increasing crash risk.

    Product
    MOBILITY VENTURES — MOBILITY VENTURES MV-1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V376000·2018-06-07

    Forest River Recalls 2017-2018 Glaval Transit Buses for Seat Belt Defect

    Forest River is recalling 2017-2018 Glaval transit buses because a washer in the driver's seat belt assembly may break, allowing the belt to separate from the vehicle.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II LOW FLOOR, ENTOURAGE, CONCORDE II, COMMUTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V380000·2018-06-07

    Volkswagen Recalls 2018 Atlas Models for Seat Belt Buckle Damage Risk

    Volkswagen is recalling 54,729 2018 Atlas vehicles because missing manual information can lead to seat belt buckle damage, increasing injury risk in crashes.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0879-2018·2018-06-06

    Poseidon Platinum 4500 Recalled for Undeclared Sildenafil and Tadalafil

    Shoreside Enterprises Inc. is recalling Poseidon Xtreme PLATINUM 4500 because FDA analysis found undeclared sildenafil and tadalafil, making it an unapproved drug.

    Product
    POSEIDON Xtreme PLATINUM 4500,1000mg, packaged in single packs sold in 24-count boxes, Distributed by: Poseidon Distribution Atlanta, GA, UPC 638632428857
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0880-2018·2018-06-06

    FDA Recalls 7K Capsules Containing Undeclared Sildenafil and Tadalafil

    The FDA is recalling 7K capsules distributed by SX Power Co. because they contain undeclared sildenafil and tadalafil, making them unapproved drugs with unestablished safety and efficacy.

    Product
    7K capsules packaged in single packs sold in 24-count boxes, Distributed by SX Power Co. San Diego, CA 92108, UPC 601577513148
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1928-2018·2018-06-06

    Maquet Datascope Recalls CARDIOSAVE Hybrid Intra-Aortic Balloon Pumps

    Maquet Datascope is recalling CARDIOSAVE Hybrid Intra-Aortic Balloon Pumps because fluid ingress can damage electronic circuit boards, preventing therapy initiation or continuation.

    Product
    CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP), Part Number 0998-00-0800-XX & 0998-UC-0800-XX (excluding 0998-00-0800-83, 0998-UC-0800-83 & 0998-00-0800-75) and cart 0997-00-1179
    Category
    Medical Device
    Distribution
    50 states
  • SevereNHTSA·18V373000·2018-06-06

    Northwood Recalls 2019 Nash Travel Trailers Due to Tire Rubbing

    Northwood is recalling 2019 Nash 24M and 29S travel trailers because tires may rub against shocks, causing damage and increasing crash risk.

    Product
    NORTHWOOD — NORTHWOOD NASH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1495-2018·2018-06-06

    Ziyad Brand Tahini Recalled for Potential Salmonella Contamination

    Ziyad Brothers Importing is voluntarily recalling Ziyad Brand Tahini in various glass jar sizes due to potential Salmonella contamination.

    Product
    Ziyad Brand Tahini, 8oz, 16oz, ¿ gal, 32oz. , packed in glass jars
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Devices)·Z-2036-2018·2018-06-06

    Recall of Sterile Powdered Surgical Gloves Due to Banned Powder Content

    WRP Asia Pacific Sdn Bhd is recalling 201,000 pairs of AmerisourceBergen sterile surgical gloves because some left-handed gloves contain powder, which is banned in the U.S.

    Product
    AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2039-2018·2018-06-06

    Torax Medical Recalls LINX Reflux Management System Implant Clasps

    Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device open or discontinuous.

    Product
    LINX Reflux Management System, Implant Clasp, 13-17 Bead, 1.5T, Product Code LXMC-xx, sterile, Rx only. Labeled as: a. Product Code LXMC-13; b. Product Code LXMC-14; c. Product Code LXMC-15; d. Product Code LXMC-16; e. Product Code LXMC-17; Laparoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V375000·2018-06-06

    Volkswagen Recalls 2018 Atlas and Tiguan for Passenger Air Bag Defect

    Volkswagen is recalling 2018 Atlas and Tiguan vehicles because the passenger frontal air bag may tear or fail to unfold properly in a crash, increasing injury risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2048-2018·2018-06-06

    Ethicon HARMONIC ACE Shears Recalled for Inadvertent Activation Risk

    Ethicon Endo-Surgery Inc is recalling HARMONIC ACE Shears because an internal component may cause continuous or inadvertent activation of the device.

    Product
    HARMONIC ACE Shears + Adaptive Tissue Technology, 5mm Diameter / 23cm Length / Curved, Product Code HAR23, GTIN 10705036014430 Product Usage: The HARMONIC ACE¿ Shears + Adaptive Tissue Technology are indicated for soft tissue incisions when bleeding control and minimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2041-2018·2018-06-06

    Torax Medical Recalls LINX Reflux Management System Implant Clasps

    Torax Medical is recalling LINX Reflux Management System implant clasps because a manufacturing defect may allow a bead to separate from the wire link, potentially rendering the device open or discontinuous.

    Product
    LINX Reflux Management System, Implant Clasp, 13-16 Bead, 1.5T, Product Code LXM-xx, sterile, Rx only. Labeled as: a. Product Code LXM-13; b. Product Code LXM-14; c. Product Code LXM-15; d. Product Code LXM-16; Laparoscopic, fundic-sparing anti-reflux procedure…
    Category
    Medical Device
    Distribution
    Distributed nationwide