The Recall Desk

State

Alabama product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30101–30125 of 80099

  • ModerateFDA (Devices)·Z-2904-2020·2020-09-02

    Neurovision Cobra EMG ET Tube Recalled for Insulating Material Softening

    Neurovision Medical Products Inc. is recalling Cobra x5 1-Ch EMG ET Tubes because the electrode insulating material may soften, potentially damaging the device and stopping signal transmission.

    Product
    Cobra x5 1-Ch EMG ET Tube, 7.0mm, REF LTE700M-5, Rx Only, Sterile EO CE UDI: B006LTE700M52/$$7061418C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2899-2020·2020-09-02

    RayCare Oncology Software Recalled for Offline Image Review Error

    RaySearch Laboratories AB is recalling RayCare oncology software due to an error message that may prevent users from accessing offline images during review tasks.

    Product
    RayCare, device is stand-alone software - Product Usage: used to support workflows and scheduling, as well as clinical information, planning and treatment management for oncology care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1539-2020·2020-09-02

    Ecolab Recalls Hand Sanitizer Due to Discoloration and Foreign Substance

    Ecolab Inc is recalling 305 drums of 55-gallon hand sanitizer nationwide due to discoloration and the presence of a foreign substance.

    Product
    Hand Sanitizer (Alcohol 80% v/v) topical solution, 55 US GAL (208 L) EcoLab Inc 1 EcoLab Place St. Paul, MN 55102 USA, NDC 47593-624-21
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1548-2020·2020-09-02

    FDA Recalls Hand Sanitizer Gel Due to Manufacturing Deviations

    Resource Recovery & Trading LLC is voluntarily recalling 17,280 bottles of hand sanitizer gel due to cGMP deviations. The product was distributed in Alabama and Georgia.

    Product
    Hand Sanitizer Disinfectant Gel 70% Ethyl Alcohol, packaged in 6.7 FL Oz. (200 mL) bottles, Distributed by: Access USA, Miami, FL 33308, UPC 650240025020
    Category
    Drug
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-1533-2020·2020-09-02

    Hikma Recalls Buprenorphine Hydrochloride Injection Due to Low Potency

    Hikma Pharmaceuticals is recalling 97,890 vials of Buprenorphine Hydrochloride Injection because stability testing revealed the drug was sub-potent.

    Product
    BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2905-2020·2020-09-02

    Neurovision Cobra EMG Endotracheal Tubes Recalled for Insulation Softening

    Neurovision is recalling Cobra x5 1-Ch EMG ET Tubes because the electrode insulating material may soften over time, potentially damaging the device and stopping EMG signal transmission.

    Product
    Cobra x5 1-Ch EMG ET Tube, 8.0mm, REF: LTE700L-5, Rx Only, Sterile EO UDI: B006LTE700L52$$7061318B - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open airway for patient ventilation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2875-2020·2020-09-02

    Ortho-Clinical Diagnostics Recalls VITROS XT Chemistry TBIL-ALKP Slides

    Ortho-Clinical Diagnostics is recalling VITROS XT Chemistry TBIL-ALKP Slides due to potential interference from etrombopag that may affect total bilirubin test results.

    Product
    VITROS XT Chemistry Products TBIL-ALKP Slides (ALKP is not affected) In Vitro Diagnostic use only - The TBIL test within the VITROS XT Chemistry Products TBIL-ALKP Slides quantitatively measures total bilirubin (TBIL) concentration in serum and plasma, Product Code: 6844296
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2874-2020·2020-09-02

    Ortho-Clinical VITROS Chemistry BuBc Slides Recalled for Etrombopag Interference

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products BuBc Slides because the drug etrombopag interferes with the test results.

    Product
    VITROS Chemistry Products BuBc Slides - in vitro diagnostic use only. VITROS Chemistry Products BuBc Slides quantitatively measure unconjugated bilirubin (Bu) and conjugated bilirubin (Bc) concentrations in serum and plasma, Product code: 8383051 (60 slide); 1612365 (18 slide)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2902-2020·2020-09-02

    Neurovision Nerveana x5 RLN Monitoring Kit Recalled for Insulation Softening

    Neurovision is recalling Nerveana x5 RLN Monitoring Kits because the electrode insulating material may soften, potentially damaging the device and stopping EMG signal transmission.

    Product
    Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube, 8.0 mm, REF NVTKIT-C8-5, Rx Only, Sterile UDIB006NVTKITC852/$$7062118C - Product Usage: For continuous EMG monitoring and status assessment of the nerves supplying the laryngeal musculature as well as providing an open…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1541-2020·2020-09-02

    Red Cross Oral Pain Relief Recalled for Cotton Pellet Labeling Error

    The Mentholatum Company is recalling Red Cross Oral Pain Relief blister packs because the included cotton pellet box incorrectly lists Natural Eugenol Oil as an ingredient.

    Product
    RED CROSS ORAL PAIN RELIEF — RED CROSS ORAL PAIN RELIEF (BENZOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2886-2020·2020-09-02

    Match Point System surgical instrument recalled due to incorrect procedure side labeling

    The Match Point System surgical instrument was recalled because the procedure side on planning reports was incorrectly marked as 'Left' instead of 'Right' for right-side procedures.

    Product
    Match Point System The Match Point System is intended to by uses as a surgical instrument to assist in the intraoperative positioning of glenoid components used with total and reverse shoulder arthroplasty by referencing anatomic landmarks of the shoulder that are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2877-2020·2020-09-02

    OraSure Benzodiazepine Micro-Plate Recalled for Incorrect Lot Number Labeling

    OraSure Technologies is recalling 13 kits of Interept Benzodiazepine Micro-Plates due to incorrect lot numbers on specification sheets and unit boxes.

    Product
    Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 2 plate Matrix Oral Fluid Coated Micro-Plate. IVD Immunoassay for Benzodiazepines, Product Number: 1110IT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2876-2020·2020-09-02

    OraSure Benzodiazepine Micro-Plate Recall Due to Incorrect Lot Number Labeling

    OraSure Technologies is recalling 39 kits of the Interept Benzodiazepine Micro-Plate EIA due to incorrect lot numbers on the specification sheet and unit box.

    Product
    Orasure Technologies Interept Benzodiazopene Miro-Plate EIA-Benzo EIA 5plate Matrix Oral Fluid Coated Micro-Plate-IVD Immunoassay for Benzodiazepines, Product Number: 1110IB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V529000·2020-09-01

    Daimler Trucks Recalls Freightliner Chassis Due to Tire Valve Stem Risk

    Daimler Trucks is recalling certain Freightliner chassis because a tire valve stem extension may contact the wheel rim, potentially causing a loss of tire pressure and increasing crash risk.

    Product
    FCCC — FCCC XCM, XCR, MC, XCL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V528000·2020-09-01

    2020-2021 BMW X5, X6, X7 Headlamp Non-Compliance Recall

    BMW is recalling certain 2020-2021 X5, X6, and X7 models because their headlamps may emit unintended blue light, which could confuse oncoming drivers and increase crash risk. Dealers will replace affected headlamps at no cost.

    Product
    BMW — BMW X6, X5, X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V527000·2020-09-01

    Engine harness defect may cause stalling in 2018–2021 Freightliner trucks

    Engine harness wires may chafe and short in certain 2018–2021 Freightliner trucks, causing unexpected engine stalling that can increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER 114SD, 108SD, BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V526000·2020-08-31

    MCI Recalls 2017-2020 J4500 Motor Coaches for Coolant Hose Failure

    Motor Coach Industries is recalling 2017-2020 J4500 motor coaches because a coolant hose may fail, causing engine shutdown and coolant spills that increase crash risk.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V521000·2020-08-28

    Heartland Bighorn Traveler landing legs may collapse causing trailer to drop

    Certain 2019-2021 Heartland Cyclone, 2020-2021 Bighorn Traveler, and 2020-2021 Elkridge recreational trailers may have insufficient bracing on the front landing legs, which could buckle and collapse while parked, causing the trailer to drop unexpectedly.

    Product
    HEARTLAND — HEARTLAND CYCLONE, ELKRIDGE, BIGHORN TRAVELER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V522000·2020-08-28

    PJ Trailers DE Trailer Hydraulic Cylinder Bolts May Fail

    PJ Trailers is recalling 2020-2021 DE model trailers. The attachment bolts securing the hydraulic cylinder may fail when the dump box is operated, creating a risk that the box could suddenly drop and injure a person.

    Product
    PJ TRAILERS — PJ TRAILERS DE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V523000·2020-08-28

    Grand Design Solitude recreational trailers recalled for propane gas leak risk

    Grand Design Solitude recreational trailers (2017-2021) are being recalled because the propane supply line may contact the refrigerator burner tube, potentially causing a propane gas leak and increasing fire risk.

    Product
    GRAND DESIGN — GRAND DESIGN SOLITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V511000·2020-08-27

    RAM 3500, 4500, 5500 Recall for Engine Oil Film Defect

    Chrysler is recalling 2019-2020 RAM 3500, 4500, and 5500 cab chassis vehicles due to a defect that can cause engine damage and fire risk.

    Product
    RAM — RAM 3500, 5500, 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide