The Recall Desk

State

Alabama product recalls

20,322 recalls have nationwide distribution and so reach Alabama. 0 additional recalls listed Alabama specifically in their distribution scope.

About recalls in Alabama

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Alabama consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11626–11650 of 20322

  • HighFDA (Devices)·Z-2640-2023·2023-10-04

    3M Attest Biological Indicators Cap May Melt During Sterilization

    3M is recalling 77,280 Attest biological indicators due to caps that may melt, deform, or crack during steam sterilization cycles, potentially compromising process validation.

    Product
    3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack, REF 41482VF; designed to qualify and monitor dynamic-air removal steam sterilization processes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2637-2023·2023-10-04

    3M Attest Biological Indicator caps may fail during steam sterilization

    3M is recalling 79,500 Attest Super Rapid Readout Biological Indicators because the cap may melt, deform, or crack during steam sterilization cycles, potentially compromising sterilization validation.

    Product
    3M Attest Super Rapid Readout Biological Indicator, REF 1492V; used to qualify or monitor dynamic-air-removal steam sterilization cycles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2639-2023·2023-10-04

    3M Attest Sterilization Indicator Caps May Melt or Crack

    3M is recalling 172,464 units of Attest biological indicators used to validate steam sterilization because caps may melt, deform, or crack during sterilization at 132°C and 135°C.

    Product
    3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack, REF 41482V; designed to qualify and monitor dynamic-air removal steam sterilization processes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2642-2023·2023-10-04

    Henke-Ject-2 Sterile Syringes Recalled for Potential Sterile Barrier Damage

    Wolf, Henke Sass is recalling Henke-Ject-2 single-use sterile syringes due to potential damage to the sterile barrier that could compromise product sterility. Approximately 216,000 units are affected across the US and Canada.

    Product
    Henke-Ject-2 part luer sterile single use syringes - used for intravenous, intramuscular, subcutaneous, intracutaneous and intraarterial injection of liquids or diluted drugs in combination with an adequate medical device or for withdrawal of fluids from the body. Ref: 4100.00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2645-2023·2023-10-04

    Stryker Recalls Expired Cinchlock SS Knotless Anchor Inserter Units

    Stryker Corporation is recalling 96 units of the expired Cinchlock SS Knotless Anchor Inserter (Part Number CAT02462, Lot 19175AE2) distributed nationwide. Expired surgical devices may not perform reliably during use.

    Product
    Cinchlock SS Knotless Anchor Inserter, Part Number CAT02462
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2638-2023·2023-10-04

    3M Attest Biological Indicators Recalled for Defective Caps

    3M is recalling specific lots of Attest biological indicators used in steam sterilization monitoring. Certain lots have caps that may melt, deform, or crack at sterilization temperatures of 132°C and 135°C, potentially compromising sterilization process verification.

    Product
    3M Attest Super Rapid Readout Steam Challenge Pack, REF 1496V; designed to qualify and monitor dynamic-air removal steam sterilization processes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2643-2023·2023-10-04

    B. Braun NORM-JECT Sterile Syringes Recalled Due to Packaging Damage

    B. Braun NORM-JECT Luer Solo 10 ml sterile syringes are recalled because blister packaging may be damaged, potentially compromising sterility. Approximately 534,000 units are affected; lot numbers 22M28C8 and 23A09C8 are included.

    Product
    B. Braun NORM-JECT Luer Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. Distributed by: Air-Tite Products Co., Inc, 565 Central Drive, Virginia Beach, VA 23454. REF: NJ-4606108-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V273000·2023-10-04

    Tiffin Allegro motorhomes recalled for faulty hydraulic slide cylinders

    Tiffin is recalling certain 2021 and 2022 Allegro and Allegro Bay motorhomes due to defective hydraulic cylinder seals. The slide-room may extend unintentionally, increasing crash risk.

    Product
    TIFFIN — 2021 TIFFIN ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2632-2023·2023-10-04

    Palindrome Chronic Catheter Kit recalls devices with incorrect length labeling

    Covidien LP is recalling Palindrome Chronic Catheter Kit devices where some catheters labeled as 23 cm implant length actually contain 28 cm devices. The mislabeling could affect proper catheter placement.

    Product
    Palindrome Chronic Catheter Kit Symmetrical Tip14.5 Fr/Ch(4.8mm)x23cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2635-2023·2023-10-04

    Ivenix Infusion System Software Startup Delays in Certain Flow Rate Ranges

    Fresenius Kabi USA has recalled Ivenix Infusion System Large Volume Pump software versions 5.0.0 and 5.0.1 due to startup time delays that may exceed 6 minutes at flow rates between 50-200 ml/hr.

    Product
    Ivenix Infusion System (IIS), Large Volume Pump (LVP) Software: 5.0.0 and 5.0.1 Part Number: LVP-SW-0004. Indicated for use in a hospital and in outpatient care environments for the controlled administration of fluids through clinically accepted routes of administration.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2644-2023·2023-10-04

    B.Braun NORM-JECT Luer Lock Solo 10ml Syringe Sterility Recall

    B.Braun NORM-JECT Luer Lock Solo 10ml sterile syringes are being recalled because the sterile blister packaging may be damaged, potentially compromising sterility. The recall affects 604,800 units distributed nationwide.

    Product
    B.Braun NORM-JECT Luer Lock Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. Distributed by: Air-Tite Products Co., Inc, 565 Central Drive, Virginia Beach, VA 23454. REF: NJ-4606728-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1178-2023·2023-10-04

    Prescription Drug Recall: Eligard Leuprolide Contains Higher Than Expected Levels

    Tolmar, Inc. is recalling Eligard (leuprolide acetate) 7.5 mg monthly injectable suspension nationwide because the constituted product contains higher than expected levels of the active ingredient. The affected lot is 13635A1 with expiration date July 31, 2024.

    Product
    ELIGARD — ELIGARD (LEUPROLIDE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2647-2023·2023-10-04

    Baxter Epiphany Cardio Server E3 Caliper Tool Non-Responsive in ECG System

    Baxter Healthcare issued an urgent correction for the Epiphany Cardio Server E3 ECG Management System because the caliper tool may become non-responsive, temporarily preventing its use. Affects 89 units distributed across the US, Canada, and Bermuda.

    Product
    Baxter Epiphany Cardio Server E3 ECG Management System Servers with software versions: a) v6.1.x, b) v6.2.x, c) v7.0.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1616-2023·2023-10-04

    Ozona Organics and Go Healthy Liquid Probiotics recalled for potential microbial growth

    Ozona Organics LLC is recalling Ozona Organics and Go Healthy Liquid Probiotics nationwide due to high water activity in the formula that could allow microbial growth. No illnesses have been reported.

    Product
    OZONA ORGANICS LIQUID PROBIOTICS & GO HEALTHY LIQUID PROBIOTICS
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1179-2023·2023-10-04

    Clearasil Rapid Rescue Deep Treatment Pads Recalled for Label Error

    RB Health (US) is recalling Clearasil Rapid Rescue Deep Treatment Pads (Salicylic Acid 2%) due to an incorrect label on the back of the packaging. The recall affects 36,426 individual units distributed nationwide.

    Product
    CLEARASIL RAPID RESCUE DEEP TREATMENT PADS — CLEARASIL RAPID RESCUE DEEP TREATMENT PADS (SALICYLIC ACID)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V164000·2023-10-03

    2022 Ford F-53 and F-59 brake caliper bolts may loosen

    Ford is recalling certain 2022 F-53 and F-59 vehicles because improperly tightened rear brake caliper bolts could loosen and damage brake lines or wheels, increasing crash risk. Dealers will inspect and repair at no cost.

    Product
    FORD — 2022 FORD F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V160000·2023-10-03

    2023 Ford Maverick missing electrical circuit affects trailer taillights

    A missing electrical circuit in certain 2023 Ford Maverick vehicles prevents trailer taillights from illuminating properly. This creates a crash risk and violates vehicle safety standards.

    Product
    FORD — 2023 FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V165000·2023-10-03

    2021-2022 Ford Bronco rearview camera image stays on after reversing

    Certain 2021-2022 Ford Broncos may display the rearview camera image after reversing, potentially distracting the driver. Ford is issuing a free software update to fix the issue.

    Product
    FORD — 2022 FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V073000·2023-10-02

    Freightliner Cascadia and Western Star trucks recalled for brake defect

    Daimler Trucks North America is recalling certain 2017-2023 Freightliner Cascadia and Western Star trucks. Corroded brake modulator valves may cause vehicles to pull to one side during braking, increasing crash risk.

    Product
    FREIGHTLINER — 2018 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V100000·2023-10-02

    2021 Porsche Taycan: Center Seat Belt Buckle May Block Child Seat Anchors

    Porsche is recalling 2020-2021 Taycan vehicles with optional rear center seats. The center seat belt buckle wiring harness may obstruct access to child seat anchors, preventing proper installation.

    Product
    PORSCHE — 2021 PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V065000·2023-10-02

    2022-2024 IC Bus School Buses Roof Panel Joint Strength Defect Recall

    Navistar is recalling certain 2022-2024 IC Bus school buses because roof panels may have insufficient joint strength and could separate during a crash, increasing injury risk. Dealers will add fasteners to secure the joints at no cost.

    Product
    IC BUS — 2022 IC BUS CE SBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V101000·2023-10-02

    2022 Freightliner Cascadia brake system failure and parking brake defect

    Daimler Trucks North America is recalling 2022 Freightliner Cascadia trucks for a software and brake hardware defect that may cause loss of braking and parking brake functionality, increasing crash risk.

    Product
    FREIGHTLINER — 2022 FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V068000·2023-10-02

    2021-2023 Thor Motor Coach RIZE and SCOPE Retractable Awning Recall

    Thor Motor Coach is recalling certain 2021-2023 RIZE and SCOPE camper vans because the retractable awning may extend unintentionally during transit. This can become a distraction or road hazard, increasing the risk of a crash.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH RIZE
    Category
    Vehicle
    Distribution
    Distributed nationwide