The Recall Desk

State

Alabama product recalls

72,936 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.

What the numbers show

Total
6,341
Critical
1,121
Severe
1,337
Most recent
2026-09-02

Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.

Which agencies issued them

These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2801–2825 of 79277

  • HighFDA (Devices)·Z-1581-2026·2026-03-25

    Leksell Gamma Knife recalled over adapter not properly aligned or locked

    Elekta is recalling Leksell Gamma Knife radiosurgery systems, covering the Perfexion, Icon and Elekta Esprit models, due to an adapter not being properly aligned or locked in place.

    Product
    Brand Name: Leksell Gamma Knife Product Description: Leksell Gamma Knife¿ Perfexion Leksell Gamma Knife¿ Icon" Leksell Gamma Knife¿ Elekta Esprit Leksell Gamma Knife¿ (available models Elekta Esprit, Icon", and Perfexion") is a radiosurgery system for use in the stereot
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1572-2026·2026-03-25

    Stryker sagittal saw attachment cover screws may loosen and detach

    Howmedica Osteonics is recalling the MICS3 Angled Sagittal Saw Attachment because the external screws securing the cover to the saw housing may loosen and detach during use.

    Product
    MICS3 Angled Sagittal Saw Attachment; Part Number: 210490
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V187000·2026-03-25

    Aston Martin DBX tire pressure warning light may not illuminate

    Aston Martin is recalling certain 2025-2026 DBX and 2026 DBX S vehicles because the tire pressure monitoring system light may not illuminate to warn drivers of underinflated tires.

    Product
    ASTON MARTIN — ASTON MARTIN DBX, DBX S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1570-2026·2026-03-25

    GE Centricity Viewer 6.0 may expose login credentials on workstations

    GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.

    Product
    Centricity Universal Viewer Software Versions 6.0 through 6.0 Sp10.4.1, a device that displays medical images (including mammograms) and data from various imaging sources, Model Numbers 2088026-406, 2100169-001, 2088026-985, 2088026-971, 2088026-614, 2088026-713, 2088026-994, 210
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03252026-01·2026-03-25

    USDA Issues Public Health Alert for Uninspected Blackwing Organic Beef and Pork

    USDA FSIS issued a public health alert for raw Blackwing organic beef and pork products produced without federal inspection. Consumers are urged to discard or return these items.

    Product
    FSIS Issues Public Health Alert for Beef and Pork Products Produced Without the Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0407-2026·2026-03-25

    Brimonidine and timolol eye drops recalled over sterility assurance failure

    Apotex is recalling two lots of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution for lack of assurance of sterility.

    Product
    BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION — BRIMONIDINE TARTRATE/TIMOLOL MALEATE OPHTHALMIC SOLUTION (BRIMONIDINE TARTRATE AND TIMOLOL MALEATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0398-2026·2026-03-25

    Dexamethasone injection failed impurity specifications at product expiry testing

    Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.

    Product
    DEXAMETHASONE SODIUM PHOSPHATE — DEXAMETHASONE SODIUM PHOSPHATE (DEXAMETHASONE SODIUM PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1573-2026·2026-03-25

    Welch Allyn vision screener display may flicker inducing photosensitive seizures

    Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.

    Product
    Brand Name: Welch Allyn, Inc. Product Name: Welch Allyn Spot Vision Screener VS100 Model/Catalog Number: VS100 Software Version: Software version 3.2.0.1 Product Description: Welch Allyn Spot Vision Screener VS100, FDA product code name: Refractometer, ophthalmic One unit pe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0579-2026·2026-03-25

    Clover Sonoma Cottage Cheese Recalled for Potential Under-Pasteurization

    Clover Sonoma low-fat cottage cheese (16 oz and 32 oz sizes) is being recalled due to potential under-pasteurization from a broken pasteurizer seal. The product may not be safe for consumption.

    Product
    CLOVER SONOMA COTTAGE CHEESE LOW FAT 2% MILKFAT NET WT 16OZ UPC 0 70852 54400 7 & 32OZ UPC 0 70852 54200 3 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952
    Category
    Food
    Distribution
    11 states
  • HighNHTSA·26V185000·2026-03-25

    Volkswagen Jetta and Taos instrument panels may not display warnings

    Volkswagen is recalling certain 2025 Jetta and Taos vehicles because the instrument panel may fail to display warning lights or gauges. This fails FMVSS 101.

    Product
    VOLKSWAGEN — VOLKSWAGEN TAOS, JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0580-2026·2026-03-25

    Clover Sonoma Sour Cream Recalled for Potential Underpasteurization

    Clover Sonoma sour cream (8 oz and 16 oz sizes) is being recalled because a broken seal on the pasteurizer may have resulted in underpasteurized product. The recall affects multiple states including California, Washington, and others.

    Product
    CLOVER SONOMA SOUR CREAM NET WT 8OZ UPC 0 70852 61800 5 & 16OZ UPC 0 70852 61500 4 DISTRIBUTED BY: CLOVER-STORNETTA FARMS LLC PETALUMA, CA 94952
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1583-2026·2026-03-25

    ConvaTec EsteemBody drainable pouch REF 423653 may leak

    ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423653, because the drainable large pouch may leak due to a manufacturing issue.

    Product
    Convatec, EsteemBody Drainable Pouch REF:423653 10-35mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1574-2026·2026-03-25

    Artegraft vascular graft recalled over incorrect lot outer packaging labeling

    LeMaitre Vascular is recalling one Artegraft Vascular Graft, REF AG740, because of a labeling mix-up resulting in the incorrect lot outer packaging of the product.

    Product
    Artegraft Vascular Graft; REF#: AG740;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1580-2026·2026-03-25

    Stryker Cub pediatric cribs sold in USA missing two warning labels

    Stryker is recalling Cub Pediatric Cribs, model FL19H, because cribs sold in the USA are missing two access door warning labels.

    Product
    Cub Pediatric Crib, Model FL19H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1587-2026·2026-03-25

    Cardiosave battery charging station left bay screw prevents full battery insertion

    Datascope is recalling the Battery Charging Station, model 0998-00-0802, because a protruding screw in the left battery bay limits full insertion of certain batteries and prevents proper charging.

    Product
    Battery Charging Station; Model: 0998-00-0802;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0569-2026·2026-03-25

    Multivitamin with Fluoride Chewable Tablets Recalled for Subpotent Vitamin D

    Winder Laboratories is recalling Multivitamin with Fluoride Chewable Tablets Grape Flavor because the product contains subpotent Vitamin D levels. The FDA discovered this deficiency during an inspection.

    Product
    Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; NDC 75826-171-10 1mg 100 TABLETS UPC 3 15826 17110 5 Manufactured by: WINDER LABORATORIES LLC Winder, GA 30680
    Category
    Drug
    Distribution
    25 states
  • SevereNHTSA·26V182000·2026-03-24

    Nova Bus driver seat belt tension device may not disengage

    Nova Bus is recalling certain 2016-2023 LFS and LFS Artic transit buses because the driver's seat belt tension-relieving device may fail to disengage without manual intervention. This fails FMVSS 208.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V180000·2026-03-24

    Lexus LX Recall: Front Passenger Air Bag May Deploy Improperly

    Toyota is recalling 2022-2024 Lexus LX vehicles because a seat frame issue may cause the front passenger air bag to deploy incorrectly during a crash.

    Product
    LEXUS — LEXUS LX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V179000·2026-03-24

    2024–2026 Toyota and Lexus vehicles load carrying capacity label incorrect

    Toyota is recalling certain 2024–2026 Toyota and Lexus vehicles because the load carrying capacity modification label may display inaccurate added weight values. Vehicles with incorrect maximum capacity weight may be overloaded, increasing crash risk.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4 HYBRID, TACOMA HYBRID, GRAND HIGHLANDER, CROWN SIGNIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V177000·2026-03-23

    Winnebago motorhome front turn signal lenses are smaller than required

    Winnebago is recalling certain 2017-2022 Brave, Itasca Sunova, Adventurer and Sunstar motorhomes because the front turn signals may have a smaller than required luminous lens area. This fails FMVSS 108.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA ADVENTURER, BRAVE, SUNSTAR, SUNOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V174000·2026-03-20

    Grand Design motorhome steps may deploy unexpectedly while in transit

    Grand Design is recalling certain 2025-2026 Lineage motorhomes because the entry door position switch may not read that the door is closed, allowing the steps to deploy unexpectedly.

    Product
    GRAND DESIGN — GRAND DESIGN LINEAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide