The Recall Desk

State

Alabama product recalls

73,824 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.

These figures cover only the 6,378 recalls whose distribution notice names Alabama specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48951–48975 of 80202

  • SevereFDA (Food)·F-1209-2017·2017-01-18

    All American Seasonings Recalls Spicy Nacho Seasoning Due to Salmonella Risk

    All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.

    Product
    Spicy Nacho. Product Code: T3552. 50 lb bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1227-2017·2017-01-18

    St. Clair Pistachio Cream Recalled for Salmonella Risk

    St. Clair Foods is recalling Pistachio Cream products due to potential salmonella contamination from an ingredient.

    Product
    Pistachio Cream, packaged under the following brands: (a) St. Clair, product code 104004, ST. CLAIR FOODS, INC., NET WT. 5 LBS (2.27 kg), MEMPHIS, TN 38116, UPC 7717114004 (b) Ron's Home Style Foods, product code 900603, NET WT. 5 LBS(2.27 kg), DIST. BY RON'S HOME STYLE FOODS…
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-0964-2017·2017-01-18

    Stryker Recalls Reprocessed Electrophysiology Catheter Cables Due to Sterility Breach

    Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheter cables because a breach in sterile packaging may have occurred, potentially rendering the product non-sterile.

    Product
    Reprocessed Electrophysiology Catheter Cables Catalog Number: CB3434CT, D134401, CB3410CT, CB3412CT Electrophysiology catheter cables are designed as electrode cables with a multi-pin connector on the distal end and the appropriate number of tails on the proximal end. The…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Devices)·Z-0987-2017·2017-01-18

    Elekta Oncentra Radiation Therapy Software Recalled for Cross Profile Defect

    Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.

    Product
    Oncentra External Beam Oncentra Brachy Product Usage: Oncentra is radiation therapy planning software designed to analyze and plan radiation treatment is three dimensions for the purpose of treating patients with cancer.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0430-2017·2017-01-18

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical peel force specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1252-2017·2017-01-18

    Roy Roger's Pancake Mix Recalled for Possible Salmonella Contamination

    House-Autry Mills is recalling Roy Roger's Pancake Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Roy Roger's Pancake Mix, Net Wt., 2 lb. 8 oz. bags, UPC Code 0 73484 22724 0
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1006-2017·2017-01-18

    Philips IQon Spectral CT Recalled for Image and Scan Errors

    Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.

    Product
    IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1225-2017·2017-01-18

    Brand Castle Monkey Bread Mix Recalled for Salmonella

    Brand Castle LLC is recalling In The Mix Monkey Bread Mix because the facility and finished product tested positive for Salmonella.

    Product
    In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY BRAND CASTLE, LLC BEDFORD HTS, OH 44146 www.brandcastle.com UPC 8 44527 03278 2
    Category
    Food
    Distribution
    38 states
  • HighFDA (Food)·F-1247-2017·2017-01-18

    House-Autry Buttermilk Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buttermilk Biscuit Mix because it contains milk from a supplier recalling product due to possible Salmonella.

    Product
    House-Autry Buttermilk Biscuit Mix Tote, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15500 9,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1007-2017·2017-01-18

    Medtronic Recalls AxIEM Touch N Go Pointer Probe for Accuracy Issues

    Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.

    Product
    AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1249-2017·2017-01-18

    House-Autry Butterflake Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling 606 bags of Butterflake Biscuit Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House-Autry Butterflake Biscuit Mix, Net Wt. 25 lb. bags, UPC Code 0 73484 20513 1,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1250-2017·2017-01-18

    Buddy's Bar-B-Q Hushpuppy Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buddy's Bar-B-Q Hushpuppy Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Buddy's Bar-B-Q Hushpuppy Mix, Net Wt., 5 lb bags, UPC Code 0 73484 22156 2,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0972-2017·2017-01-18

    Siemens Recalls Artis Q Angiographic X-Ray Systems for Generator Defects

    Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.

    Product
    Artis Q/Q.zen, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0988-2017·2017-01-18

    ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk

    ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.

    Product
    Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0963-2017·2017-01-18

    Stryker Recalls Reprocessed Ablation Catheter Cables Due to Sterility Concerns

    Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.

    Product
    Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as electrode cables with a multi-pin connector on the distal end which connects to an ablation catheter and a multi-pin connector on the proximal end which connects…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1248-2017·2017-01-18

    House-Autry Cheese Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Cheese Biscuit Mix because it contains milk from a supplier recalling product for possible Salmonella.

    Product
    House-Autry Cheese Biscuit Mix, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15510 8,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1005-2017·2017-01-18

    Philips Clinix RF Plus X-ray System Recalled for Tilt Hazard

    Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.

    Product
    FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V040000·2017-01-18

    Nissan Recalls 2015-2017 Altima Vehicles for Rear Door Latch Defect

    Nissan is recalling 2015-2017 Altima vehicles because improperly routed rear door latch cables may allow doors to open while driving, increasing injury risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1013-2017·2017-01-18

    Beckman Coulter Recalls UniCel DxH 800 Cellular Analysis System

    Beckman Coulter is recalling the UniCel DxH 800 Cellular Analysis System because it may fail to detect blasts in some blood samples.

    Product
    UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1246-2017·2017-01-18

    House Autry Corn Bread Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling House Autry Stone Ground Buttermilk Corn Bread Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House Autry, stone Ground Buttermilk Corn Bread Mix, Net wt. 8 oz. boxes, UPC Code 0 73484 15512 2,
    Category
    Food
    Distribution
    7 states
  • ModerateFDA (Devices)·Z-0965-2017·2017-01-18

    ASP Recalls EVOTECH Endoscope Cleaner Due to Hose Leak Risk

    Advanced Sterilization Products is recalling 107 EVOTECH Endoscope Cleaner and Reprocessor Systems because a hose may come loose and cause a leak.

    Product
    EVOTECH Endoscope Cleaner and Reprocessor System 208V, Product Code: 50004 The EVOTECH ECR Endoscope Cleaner and Reprocessor, a washer/disinfector, is indicated for use with high-level disinfectant CIDEX OPA Concentrate Solution and an enzymatic detergent (CIDEZYME XTRA) to…
    Category
    Medical Device
    Distribution
    Distributed nationwide