The Recall Desk

State

Alabama product recalls

73,737 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.

These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33151–33175 of 80114

  • CriticalFDA (Food)·F-0418-2020·2020-01-01

    Fuji Food Products Recalls Okami Supreme California Rolls for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Supreme California Rolls due to potential Listeria monocytogenes contamination. Consumers should not eat the product.

    Product
    Okami brand 8pc Supreme California Roll, SKU 28103
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0420-2020·2020-01-01

    Fuji Food Products Recalls Okami Spicy California Rolls for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Spicy California Rolls due to potential Listeria monocytogenes contamination. Consumers should discard or return the product.

    Product
    Okami brand 8pc Spicy California Roll, SKU 28102
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0424-2020·2020-01-01

    Okami Brown Rice California Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Brown Rice Classic California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Okami brand 8pc Brown Rice Classic California Roll, SKU 28122
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0429-2020·2020-01-01

    FDA Recalls Okami Salmon Philly Rolls Due to Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Salmon Philly Rolls because they may be contaminated with Listeria monocytogenes.

    Product
    Okami brand 8pc Salmon Philly Roll, SKU 28113
    Category
    Food
    Distribution
    31 states
  • CriticalFDA (Food)·F-0425-2020·2020-01-01

    Okami Sushi Platter Recalled for Potential Listeria Contamination

    Fuji Food Products is recalling Okami brand 25pcs Sushi Platters due to potential Listeria monocytogenes contamination. Consumers should not consume the product.

    Product
    Okami brand 25pcs Sushi Platter, SKU 28200
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Food)·F-0432-2020·2020-01-01

    Trader Joe's Shrimp Spring Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's Shrimp Spring Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's Shrimp Spring Rolls 7oz, SKU 908795
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Food)·F-0428-2020·2020-01-01

    Fuji Food Products Recalls Okami Tempura Shrimp Rolls Due to Listeria Risk

    Fuji Food Products is recalling Okami OK Tempura Shrimp Roll products because they may be contaminated with Listeria monocytogenes. The recall covers units distributed in multiple states.

    Product
    Okami OK Tempura Shrimp Roll, 6pc w/ Sweet and Dynamite Sauce, SKU 28114
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Devices)·Z-0561-2020·2020-01-01

    LivaNova SenTiva VNS Therapy Generators Recalled for Potential Device Reset

    LivaNova is recalling SenTiva VNS Therapy generators that may reset and become disabled within 60 days of enabling, potentially requiring additional surgery or causing a return of symptoms.

    Product
    VNS Therapy, SenTiva, Model # 1000, (01)05425025750405, Rx Only for vagal nerve stimulation (VNS) therapy
    Category
    Medical Device
    Distribution
    44 states
  • SevereFDA (Food)·F-0419-2020·2020-01-01

    FDA Recalls Okami California Rolls Due to Listeria Risk

    Fuji Food Products is recalling Okami brand 8pc Supreme California Rolls because they may be contaminated with Listeria monocytogenes.

    Product
    Okami brand 8pc Supreme California Roll, SKU 28103
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Food)·F-0412-2020·2020-01-01

    Trader Joe's Spicy California Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's Spicy California Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pcs Spicy California Roll, 8oz, SKU 00348966T
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Food)·F-0433-2020·2020-01-01

    Trader Joe's Tofu Spring Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's Tofu Spring Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's Tofu Spring Rolls 7oz, SKU 921510
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Food)·F-0415-2020·2020-01-01

    Trader Joe's Smoked Salmon Philly Rolls Recalled for Listeria Risk

    Fuji Food Products is recalling Trader Joe's Smoked Salmon Philly Rolls due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's 8pcs Smoked Salmon Philly Roll, SKU 603775
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Food)·F-0427-2020·2020-01-01

    Fuji Food Products Recalls Seafood Combo for Listeria Risk

    Fuji Food Products is recalling Okami 8pc Seafood Combo products due to potential Listeria monocytogenes contamination.

    Product
    Okami 8pc SEAFOOD COMBO 6 SURIMI 2 EBI SHRIMP, SKU 28262
    Category
    Food
    Distribution
    31 states
  • SevereFDA (Food)·F-0434-2020·2020-01-01

    Trader Joes Queso Fundido 16oz Recalled for Listeria Contamination

    Trader Joes Queso Fundido 16oz is recalled due to potential Listeria monocytogenes contamination. The product was distributed in multiple states.

    Product
    Trader Joes Queso Fundido 16oz, SKU 646574
    Category
    Food
    Distribution
    31 states
  • HighFDA (Devices)·Z-0744-2020·2020-01-01

    Axis-Shield Homocysteine Reagent Recalled for Potential Performance Issues

    Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential performance issues detected during routine testing.

    Product
    Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHRWR1000 - Product Usage: The device can assist in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria. The device is intended for Professional use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0724-2020·2020-01-01

    Bard Max-Core Biopsy Instrument Recalled for Firing Failures

    Bard Peripheral Vascular Inc is recalling 727,034 units of the Bard Max-Core Disposable Core Biopsy Instrument due to complaints of failure to fire and failure to obtain samples.

    Product
    BARD MAX-CORE Disposable Core Biopsy Instrument - Product Usage: The core needle biopsy device is intended for use in obtaining biopsies from soft tissues such as liver, kidney, prostate, spleen, lymph nodes and various soft tissue tumors. It is not intended for use in bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0736-2020·2020-01-01

    RayStation Radiation Therapy Software Recalled for Beam Editing Bug

    RaySearch Laboratories is recalling RayStation software versions 4.0 through 9.0 because a bug may reset beam settings, requiring dose recalculation.

    Product
    RayStation stand-alone software treatment planning system, Model Numbers 4.0, 4.5, 4.7, 4.9, 5.0, 6.0, 6.1, 6.2, 6.3, 7.0, 8.0, 8.1, 9.0 - Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0719-2020·2020-01-01

    3M Recalls Durapore Advanced Surgical Tape Due to Bond Failure Risk

    3M is recalling Durapore Advanced Surgical Tape because long-term exposure to high moisture may cause bond failure and fiber fraying, posing a risk of accidental ingestion or aspiration.

    Product
    3M Durapore Advanced, Surgical Tape, Model Numbers: 1590-0, 1590-1, 1590-2, 1590-3, 1591-0, 1591-1, 1591-2, 1591-3, 1590S-1, 1590S-2, 1590B-118, 1590B-136
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0728-2020·2020-01-01

    Cardinal Health Recalls S.M.A.R.T. Stents for Incorrect MRI Labeling

    Cardinal Health is correcting labeling on S.M.A.R.T. Nitinol Stent Systems that incorrectly stated they were 'MRI Safe' instead of 'MRI Conditional'.

    Product
    S.M.A.R.T. Nitinol Stent System and the S.M.A.R.T. Control Nitinol Stent System. The SMART stent system includes a self-expanding stent made of Nitinol (nickel-titanium alloy) material and a 6 French (2.0 mm) or 7 French (2.3 mm) sheathed delivery system. The stent is laser…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0743-2020·2020-01-01

    Axis-Shield Homocysteine Reagent Recalled for Potential Performance Issues

    Axis-Shield Diagnostics is recalling 740 units of Liquid Stable 2-Part Homocysteine Reagent due to potential performance issues detected during routine testing.

    Product
    Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT, Part Number FHRWR100 - Product Usage: The device can assist in the diagnosis and treatment of patients suspected of having hyperhomocysteinemia and homocystinuria. The device is intended for Professional use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0737-2020·2020-01-01

    Diagnostica Stago Recalls STA Unicalibrator Due to Positive Bias

    Diagnostica Stago is recalling 5,498 units of STA Unicalibrator because a positive bias was confirmed when compared to International Standards.

    Product
    STA UNICALIBRATOR (ref. 00675)
    Category
    Medical Device
    Distribution
    42 states