The Recall Desk

State

Alabama product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51176–51200 of 80211

  • ModerateFDA (Drugs)·D-1501-2016·2016-09-21

    Amerisource Recalls bupropion Hydrochloride Tablets for Dissolution Failure

    Amerisource Health Services is recalling 2,626 bottles of bupropion hydrochloride extended-release tablets due to failed dissolution specifications.

    Product
    buPROPion Hydrochloride Extended-Release Tablets, USP (XL), 300mg, 500-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India For BluePoint Laboratories, NDC 68001-264-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2793-2016·2016-09-21

    Siemens Syngo Plaza PACS Recall for Measurement Display Suffix

    Siemens is recalling 101 Syngo Plaza PACS systems because a suffix on DICOM images may indicate that displayed measurements differ from actual values.

    Product
    Syngo Plaza picture archiving and communication system (PAC) (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2770-2016·2016-09-21

    Sysmex Fluorocell PLT Reagent Recalled for Potential Low Platelet Results

    Sysmex America Inc is recalling Fluorocell PLT reagent because it may produce falsely low platelet results on Sysmex XN-Series analyzers.

    Product
    Fluorocell PLT reagent, Catalog #CD994563 Fluorocell PLT is used to stain platelets in a diluted blood sample for the counting of platelets with the Sysmex XN-Series automated hematology analyzers
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2794-2016·2016-09-21

    Siemens Syngo.Plaza VB 10 A PACS Recall for Measurement Suffix Display

    Siemens is recalling 101 Syngo.Plaza VB 10 A image processing systems because a suffix on DICOM images may indicate that displayed measurement values differ from real values.

    Product
    Syngo.Plaza VB 10 A, image processing system (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2804-2016·2016-09-21

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Calibrator Kit 31

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 31, Lot 3155, because an incorrect value on the Assay Data Disks prevents successful calibration of the HbA1c assay.

    Product
    The VITROS¿ Chemistry Products Calibrator Kit 31, Lot 3155 used in conjunction with: VITROS¿ Chemistry Products HbA1c Reagent Kit, Generation 6 (GEN 6) and Assay Data Disk (ADD), Data Release Versions (DRV) 5873, 5874, 5875, or 5876, is used to calibrate the VITROS 5,1 FS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2779-2016·2016-09-21

    Biomerieux Recalls VIDAS NT-pro-BNP Kits Due to Packaging Error

    Biomerieux is recalling 229 VIDAS NT-pro-BNP kits because they contain the incorrect number of control vials.

    Product
    VIDAS NT-pro-BNP Product Usage: VIDAS¿ NTproBNP (PBNP) is an automated quantitative test for use on the instruments of the VIDAS family for the determination of N terminal fragment of Btype natriuretic peptide in human serum or plasma (lithium heparin) using the ELFA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2778-2016·2016-09-21

    Alere LDX Optical Check Cassettes Recalled for Incorrect Expiration Date

    Alere San Diego, Inc. is recalling LDX Optical Check Cassettes because the expiration date on the magnetic strip does not match the labeled date.

    Product
    LDX Optical Check Cassettes (OCC) Model Number: 10-228 and 14-535 Cassette in box with foam insert. The cassette is used to check the optics system of the LDX analyzer. Product Usage: The Optics Check Cassette is used to check the optics system of the Alere Cholestech…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V678000·2016-09-20

    New Flyer Recalls 2016 XN60 and XN40 Buses for CNG Defect

    New Flyer is recalling 38 model year 2016 XN60 and XN40 transit buses because a pressure relief device may fracture, releasing high-pressure gas and increasing fire risk.

    Product
    NEW FLYER — NEW FLYER XN60, XN40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V679000·2016-09-20

    Ducati Recalls XDiavel Motorcycles for Loose Final Drive Pulley Nut

    Ducati is recalling 2016-2017 XDiavel motorcycles because a loose final drive pulley nut may cause loss of power to the rear wheel, increasing crash risk.

    Product
    DUCATI — DUCATI XDIAVEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E073000·2016-09-20

    Porsche Brake Fluid Recall Due to Missing DOT 4 Labeling

    Porsche is recalling specific 1L and 30L brake fluid containers manufactured between September 2015 and August 2016 because they lack the required 'DOT 4' label, posing a risk of incompatible fluid use.

    Product
    SERVICE BRAKES, HYDRAULIC:FLUID recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V680000·2016-09-20

    Porsche Recalls 2017 Macan Models Due to Front Suspension Defect

    Porsche is recalling 2017 Macan models because front anti-rollbar links may move out of position, causing oversteer and increasing crash risk.

    Product
    PORSCHE — PORSCHE MACAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16267·2016-09-20

    Denon Recalls HEOS 1 Go Pack Battery Packs for Fire and Burn Hazards

    Denon is recalling HEOS 1 Go Pack rechargeable battery packs because they can overheat, posing fire and burn hazards. No injuries have been reported.

    Product
    HEOS 1 Go Pack rechargeable battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V675000·2016-09-19

    Mitsubishi Recalls 2017 Mirage Vehicles for Headlight Adjustment Defect

    Mitsubishi is recalling 2017 Mirage vehicles with HID headlamps because the horizontal adjustment clips may not be secured, potentially reducing visibility or blinding oncoming drivers.

    Product
    MITSUBISHI — MITSUBISHI MIRAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·083-2016·2016-09-17

    Gallo Meats Recalls Sausage, Beef, and Lamb Products Lacking Federal Inspection

    Gallo Meats LLC is recalling approximately 82 pounds of sausage, beef, and lamb products produced without federal inspection. The hot Italian sausage may also contain undeclared allergens.

    Product
    Gallo Meats LLC. Recalls Sausage, Beef and Lamb Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·081-2016·2016-09-16

    Tucson Tamale Wholesale Recalls Beef Tamales Lacking Federal Inspection

    Tucson Tamale Wholesale Company is recalling 915 pounds of beef tamales because the meat was produced without federal inspection. No illnesses have been reported.

    Product
    Tucson Tamale Wholesale Company LLC — Tucson Tamale Wholesale Company, LLC Recalls Beef Tamale Products Containing Meat Produced Without Benefit of Federal Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V672000·2016-09-16

    Toyota Recalls 2016 Prius Vehicles Due to Air Bag Inflation Error

    Toyota is recalling 7,817 model year 2016 Prius vehicles because a manufacturing error may cause the front passenger air bag to partially inflate unintentionally.

    Product
    TOYOTA — TOYOTA PRIUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V671000·2016-09-16

    Jayco Recalls 2017 Octane Travel Trailers for Incorrect Tire Labels

    Jayco is recalling 2017 Octane Super Lite travel trailers because incorrect tire labels may lead to over-inflation and sudden tire failure.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER OCTANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V673000·2016-09-16

    Forest River Recalls 2017 Salem and Wildwood Trailers for Incorrect Tire Placards

    Forest River is recalling 2017 Salem and Wildwood recreational trailers because the Federal Placard lists incorrect tire and rim specifications, which may lead to under-inflation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16264·2016-09-15

    Polaris Recalls Ranger 900 Vehicles Due to Fire and Burn Hazards

    Polaris is recalling about 42,500 model year 2014 Ranger 900 vehicles because a heat shield can fall off, creating fire and burn risks.

    Product
    Polaris Ranger 900 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16265·2016-09-15

    GE Profile Top-Loading Clothes Washers Recalled for Fire Hazard

    GE Appliances is recalling about 222,000 Profile top-loading clothes washers because an electrical component can overheat and cause a fire.

    Product
    GE Profile™ top-loading clothes washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16266·2016-09-15

    Samsung Recalls Galaxy Note7 Smartphones Due to Fire and Burn Hazards

    Samsung is recalling Galaxy Note7 smartphones sold before September 15, 2016, because the lithium-ion battery can overheat and catch fire, posing a burn hazard.

    Product
    Samsung Galaxy Note7 smartphones sold prior to September 15, 2016
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V668000·2016-09-15

    Chrysler Recalls Vehicles Due to Potential Airbag and Seat Belt Failure

    Chrysler is recalling specific 2010-2014 models because a module may short circuit, preventing airbags and seat belt pretensioners from deploying in a crash.

    Product
    JEEP — JEEP, DODGE, CHRYSLER COMPASS, CALIBER, PATRIOT, SEBRING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V669000·2016-09-15

    Starcraft RV Recalls 2017 AR-ONE MAXX Trailers Due to Incorrect Axle Labeling

    Starcraft RV is recalling 40 model year 2017 AR-ONE MAXX LE trailers because the Federal label incorrectly states they have two axles instead of one, creating an overload risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT AR-ONE MAXX
    Category
    Vehicle
    Distribution
    Distributed nationwide