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.

Which agencies issued them

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.

49376–49400 of 80202

  • HighFDA (Devices)·Z-0898-2017·2016-12-28

    Teleflex Recalls Mucosal Atomization Devices Due to Incomplete Atomization

    Teleflex Medical is recalling Mucosal Atomization Devices because they may produce a straight stream instead of a fully atomized plume of medication.

    Product
    Mucosal Atomization Device (MAD), Intranasal Mucosal Atomization Device with 3mL Syringe and Vial Adapter; Product Code MAD100, MAD100OS MAD110, MAD110OS, MAD130, MAD130OS, MAD140, MAD140OS, MAD300, MAD300B. Manufactured By: Wolfe-Tory Medical, Inc., Teleflex Medical. For…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V938000·2016-12-28

    Navistar Recalls 2017 International Trucks Due to Battery Latch Fire Risk

    Navistar is recalling 2017 International ProStar, LoneStar, 9900i, and TranStar trucks because a battery latch may cause an electrical short and fire.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LONESTAR, 9900I, TRANSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0784-2017·2016-12-28

    Ultroid Procedure Pack Recalled for Quality System Non-Compliance

    Ultroid Technologies is recalling 52,084 procedure packs because they were not manufactured under required quality system controls.

    Product
    Ultroid Procedure Pack including the Ultroid Sterile Disposable Probes.
    Category
    Medical Device
    Distribution
    34 states
  • HighFDA (Devices)·Z-0877-2017·2016-12-28

    BD SurePath Collection Vials Recalled Due to Cracked Caps

    Becton Dickinson is recalling SurePath collection vials because cracked caps may allow preservative fluid to leak.

    Product
    BD SurePathTM Preservative Collection Vials, catalog numbers 490505, 490527, 491095, 491096, and 491097. SurePath¿ Preservative Fluid is designed for use with the PrepStain¿ System. SurePath¿ Preservative Fluid is an alcohol-based, preservation solution that serves as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0774-2017·2016-12-28

    AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk

    AngioDynamics is recalling 751 Stiffened Micro-Introducer Kits because a component may detach during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO B PG, Item Number H787065970505, Catalog No.REF 06597050, 2) 4 F Stiffened Micro-Introducer Kit, 45CM NT/T ECHO S PG, Item Number H787065970525, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0870-2017·2016-12-28

    Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion

    Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.

    Product
    8470-009-030 3.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0812-2017·2016-12-28

    Brownwood Farms Recalls BBQ Mustard Glaze for Undeclared Soy

    Brownwood Farms is recalling BBQ Mustard Glaze because it contains soy ingredients not declared on the label.

    Product
    Brownwood Farms BBQ Mustard Glaze. 11oz glass bottles and 1 gallon. Private labels: Kimmel Orchard & Vineyard (Barbeque Mustard 11oz)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0781-2017·2016-12-28

    Nuvectra Recalls Algovita Spinal Cord Stimulation Leads Due to Stylet Protrusion

    Nuvectra is recalling Algovita Spinal Cord Stimulation System percutaneous leads because the stylet may protrude beyond the distal lead tip.

    Product
    Algovita Spinal Cord Stimulation System, Percutaneous Leads, 8-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Leads, 12-Electrode Percutaneous Lead Kit; Algovita Spinal Cord Stimulation System Percutaneous Trial Leads, 8-electrode…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0763-2017·2016-12-28

    Fresh Express Caesar Salad Kits Recalled for Undeclared Walnuts

    Fresh Express is recalling Caesar salad kits because the condiment packets contain undeclared walnuts, a tree nut allergen.

    Product
    Fresh Express Kit Caesar salad, Net Wt. 7.6 oz. (215g), Fresh Express Incorporated, 550 S. Caldwell St. Charlotte, NC 28202, packed in clear flexible plastic bags. Product Code: G163B13A
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-0886-2017·2016-12-28

    Amendia Recalls Black Widow Spinal Plates Due to Mating Feature Defect

    Amendia, Inc. is recalling 48 units of Black Widow Buttress Plates due to a design defect in the mating feature between the plate and screw.

    Product
    Black Widow Plate 19mm Plate, Part Number TBP119; Black Widow Plate 23mm Plate, Part Number TBP123 The Black Widow Buttress Plates and Screws are designed for preventing migration or expulsion of allograft or autograft in the thoracolumbar to S1 Spinal region
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0869-2017·2016-12-28

    Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion

    Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.

    Product
    8450-107-525 2.5MM Precision Match Head, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0871-2017·2016-12-28

    Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion

    Stryker Instruments is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.

    Product
    8470-009-040 4.0MM Precision Round, 16CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0816-2017·2016-12-28

    Brownwood Farms Jalapeno Cherry Butter Recalled for Undeclared Yellow #5

    Brownwood Farms is recalling Jalapeno Cherry Butter because it contains Yellow #5, an ingredient not declared on the label.

    Product
    Brownwood Farms Jalapeno Cherry Butter. 12oz glass bottles and 1 gallon.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0813-2017·2016-12-28

    Brownwood Farms Apple Riesling Salsa Recalled for Undeclared Yellow 5

    Brownwood Farms is recalling Apple Riesling Salsa because it contains Yellow 5, an ingredient not declared on the label.

    Product
    Brownwood Farms Apple Riesling Salsa. 21oz glass bottles and 1 gallon. Private labels: Arbor Day Farm (Apple Riesling Salsa 21oz). Kimmel Orchard & Vineyard (Apple Riesling Salsa 21oz). St. Julian Winery (Apple Riesling Salsa 19oz).
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0873-2017·2016-12-28

    Stryker Recalls Sterile Minimally Invasive Surgery Burs Due to Corrosion

    Stryker is voluntarily recalling specific lots of sterile MIS Toolsteel Burs because they may exhibit signs of corrosion.

    Product
    8450-009-030 3.0MM Precision Round, 13CM, single use, Sterile The Stryker MIS (Minimally Invasive Surgery) product offering, is used to remove osseous material during surgical cases. Each cutting accessory consists of: " A shank (B) with a notch (A), that fits in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0814-2017·2016-12-28

    Brownwood Farms Peach Salsa Recalled for Undeclared Yellow 5 Ingredient

    Brownwood Farms is recalling Peach Salsa because it contains Yellow 5, a color additive not declared on the label.

    Product
    Brownwood Farms Peach Salsa. 17oz glass bottles. Private labels: Bowers Harbor Vineyard (Peach Salsa 12oz). Crossroads.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0824-2017·2016-12-28

    Stanmore Implants Recalls DF Coated Integral Shaft and Stem Components

    Stanmore Implants Worldwide Ltd. is recalling 15 units of DF Coated Integral Shaft & Stem components due to packaging punctures reported by customers.

    Product
    DF Coated Integral Shaft & Stem 15x30x38; DF Coated Integral Shaft & Stem 15x36x44; DF Coated Integral Shaft & Stem 30x30x38; DF Coated Integral Shaft & Stem 30x36x44 The product is a component is a systems that is intended for the replacement if diseased or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0771-2017·2016-12-28

    Teleflex Recalls RUSCH Pocket PAC Intermittent Catheter Kits Due to Labeling Error

    Teleflex Medical is recalling RUSCH Pocket PAC Intermittent Catheter Kits because they are labeled with expiration dates that exceed the validated shelf life.

    Product
    RUSCH, Pocket PAC IC Intermittent Cath Kit, 8 FR, 12 FR, 14 FR, 10 FR and 16 FR, Rx Only, Sterile, Intermittent self-catheterization
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0772-2017·2016-12-28

    AngioDynamics Recalls Percutaneous Introducer Sets Due to Detachment Risk

    AngioDynamics is recalling 162 boxes of Stiffened Micro-Introducer Kits because the rotating luer may detach from the dilator hub during use.

    Product
    ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5 F Stiffened Micro-Introducer Kit, 45CM SS/SS ECHO B PG, Item Number H787065970395, Catalog No.REF 06597039, 2) 5 F Stiffened Micro-Introducer Kit, STF 5F M.I. KIT 45CM SS/SS ECHO S PG, Item Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0820-2017·2016-12-28

    Stanmore Tibial Component Fixed Hinge Recall Due to Pouch Puncture

    Stanmore Implants Worldwide Ltd. is recalling 13 units of Tibial Component Fixed Hinge Small Long and Short due to punctured packaging.

    Product
    Tibial Component Fixed Hinge Small Long; Tibial Component Fixed Hinge Small Short The product is a component is a systems that is intended for the replacement if diseased or deficient bone around the knee joint, distal femur, proximal femur or total femur bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0231-2017·2016-12-28

    Sage Products Recalls Chlorhexidine Gluconate Cloth Due to CGMP Deviations

    Sage Products LLC is recalling 2% Chlorhexidine Gluconate Cloth due to CGMP deviations and potential contamination. The product was distributed nationwide and internationally.

    Product
    CHLORHEXIDINE GLUCONATE — CHLORHEXIDINE GLUCONATE (CHLORHEXIDINE GLUCONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0384-2017·2016-12-28

    Teleflex Medical Recalls LMA MADgic Atomization Devices for Spray Defect

    Teleflex Medical is recalling LMA MADgic atomization devices because they may produce a straight stream instead of an atomized plume, potentially causing inadequate anesthesia.

    Product
    LMA MADgic, Atomization Device with 3mL Syringe, Rx only, Product Usage: These products are used for the delivery of topical anesthesia via an atomized spray to the oral, nasal, pharyngeal or laryngeal mucosa. Teleflex Medical is recalling these products as they may produce…
    Category
    Medical Device
    Distribution
    Distributed nationwide