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.

Which agencies issued them

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.

42276–42300 of 80187

  • ModerateFDA (Drugs)·D-0710-2018·2018-05-09

    Rhodes Pharmaceuticals Recalls Aptensio XR Capsules Due to Dissolution Failure

    Rhodes Pharmaceuticals is recalling Aptensio XR capsules because they failed to meet dissolution specifications. The affected lot was distributed nationwide.

    Product
    Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only 90-count bottle. Marketed by: Rhodes Pharmaceuticals L.P., Coventry, RI 02816. Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834. NDC 42858-402-45
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1611-2018·2018-05-09

    Roche OMNI S4 Analyzer Recalled for Software Scheduler Failure

    Roche Diagnostics is recalling 1,026 OMNI S4 analyzers because a software defect prevents the AutoQC scheduler from activating.

    Product
    Cobas b 221<4>Roche OMNI S4 system; Catalog numbers: 3337138001 and 3337138692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1627-2018·2018-05-09

    Nanosil Spray Gel Recalled for Manufacturing Deficiencies and Missing Expiration Dates

    Conseal International is recalling 384 units of Nanosil Spray Gel due to FDA inspection findings of manufacturing deficiencies and missing expiration dates.

    Product
    Nanosil Spray Gel, "***IMMUNE SYSTEM SUPPORT***ENGINEERED NANO-SILVER SOLUTION***", Net. Wt. 4 fl. oz./118mL, Catalog No. NSP-04 The product is a topical spray used to treat discomfort and other pathological conditions affecting exposed soft tissues of the body caused by…
    Category
    Medical Device
    Distribution
    3 states
  • ModerateFDA (Devices)·Z-1584-2018·2018-05-09

    CooperSurgical Recalls 5 mm Apple-Hunt Secondary Cannulas Due to Packaging Error

    CooperSurgical, Inc. is recalling 520 units of 5 mm Apple-Hunt Secondary Cannulas because they were packaged with the wrong trocar length type.

    Product
    5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage: The Apple-Hunt Secondary Cannulas are indicated for use in laparoscopic surgical procedures to provide a pathway for the introduction of endoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1612-2018·2018-05-09

    Roche OMNI S6 Analyzer Software Defect Recalled by FDA

    Roche Diagnostics is recalling 1,026 OMNI S6 analyzers because a software defect prevents scheduled AutoQC measurements from starting.

    Product
    cobas b 221<6>Roche OMNI S6 system; Catalog numbers: 3337154001 and 3337154692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1589-2018·2018-05-09

    Philips Allura Xper and UNIZ Systems Recalled for Monitor Freezing

    Philips is recalling 682 Allura Xper and UNIZ interventional fluoroscopic x-ray systems because the large screen monitor may freeze for 15 seconds after continuous operation.

    Product
    Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray system Product Usage: The Allura Xper ED series is intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging…
    Category
    Medical Device
    Distribution
    44 states
  • ModerateFDA (Devices)·Z-1615-2018·2018-05-09

    IntroMedic Recalls Miriam Capsule Endoscope System Due to Battery Indicator Error

    IntroMedic Co., Ltd. is recalling 82 units of the Miriam Capsule Endoscope System because the battery indicator may incorrectly display orange when the battery is fully charged.

    Product
    Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for visualization of the small bowel mucosa. It may be used as a tool in the detection of abnormalities of the small bowel in adults.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18150·2018-05-08

    Hauck Recalls Nerf Battle Racer Go-Karts Due to Steering Wheel Hazards

    Hauck is recalling Nerf Battle Racer go-karts because the steering wheel can detach, break, or crack, posing laceration and collision risks to children.

    Product
    Hauck Nerf® Battle Racer go-karts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V301000·2018-05-08

    Thomas Built Buses Minotour Recalled for Wheelchair Lift Wiring Defect

    Daimler Trucks North America is recalling 2002-2018 Thomas Built Buses Minotour school buses with wheelchair lifts due to a wiring defect that allows the lift to operate while the vehicle is in motion.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V300000·2018-05-08

    Freightliner Recalls Cascadia Trucks Due to Air Bag Fastener Defect

    Daimler Trucks North America is recalling 2018-2019 Freightliner Cascadia vehicles because driver's air bag fasteners may not be installed correctly, potentially affecting deployment.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V299000·2018-05-07

    Nova Bus Recalls 2015-2017 LFS Models Due to Brake Component Defect

    Nova Bus is recalling 2015-2017 LFS and LFS Artic transit buses because a brake guide pin may break, potentially causing loss of braking ability or tire pressure.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V296000·2018-05-04

    Forest River Surveyor Recalled for Refrigerator Overheating Fire Risk

    Forest River is recalling 2018 Surveyor recreational trailers because a missing fan in the slide-out refrigerator may cause overheating and increase the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V298000·2018-05-04

    Entegra Recalls 2019 Vision and Emblem Motorhomes for Wiper Defect

    Entegra is recalling 2019 Vision and Emblem motorhomes because the windshield wiper motor may fail in heavy snow or ice, reducing driver visibility.

    Product
    ENTEGRA — ENTEGRA VISION, EMBLEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V295000·2018-05-03

    GM Recalls 2014-2017 Chevrolet Express and GMC Savana for Fire Risk

    General Motors is recalling 2014-2017 Chevrolet Express and GMC Savana vans because liquid leakage in the driver's window switch can cause corrosion and increase the risk of a fire.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V287000·2018-05-03

    Porsche Recalls 2015 918 Spyder for Rear Suspension Control Arm Defect

    Porsche is recalling 2015 918 Spyder vehicles because rear suspension connecting shafts may fail due to stress corrosion cracking, increasing the risk of a crash.

    Product
    PORSCHE — PORSCHE 918 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V286000·2018-05-03

    Jayco Recalls 2018 Eagle Fifth Wheel Trailers Due to Pin Box Defect

    Jayco is recalling 2018 Eagle HT fifth wheel trailers because a spindle placement error in the pin box may cause the bearing to become loose, increasing the risk of a crash.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V290000·2018-05-03

    Navistar Recalls 2019 IC Bus CE School Buses Due to Brake Line Routing

    Navistar is recalling 2019 IC Bus CE school buses because an improperly routed air supply line may cause unintentional parking brake modulation, increasing crash risk.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V288000·2018-05-03

    Daimler Recalls 2017 Sprinter Vans for Missing Structural Welds

    Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vans because missing spot welds may reduce body strength in a crash.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V291000·2018-05-03

    GM Recalls 2015-2016 Chevrolet Tahoe and Silverado 1500 for Seat Belt Cable Defect

    General Motors is recalling 2015-2016 Chevrolet Tahoe and Silverado 1500 Police Pursuit and Special-Service vehicles because the driver's seat belt pretensioner cable may fatigue and break, increasing injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET TAHOE, SILVERADO 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V292000·2018-05-03

    Jayco Jay Series Trailers Recalled for Roof Lift Mechanism Defect

    Jayco is recalling 2011 and 2013 Jay Series camping trailers because misuse of the manual roof lift override may damage the mechanism, causing the roof to fall unexpectedly.

    Product
    JAYCO — JAYCO JAY SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1410-2018·2018-05-02

    Rose Acre Farm Shell Eggs Recalled for Salmonella Braenderup Risk

    Rose Acre Farm is recalling shell eggs due to potential Salmonella Braenderup contamination. The recall affects direct consignees in 13 states.

    Product
    Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)
    Category
    Food
    Distribution
    13 states