The Recall Desk

State

Alabama product recalls

20,199 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.

8651–8675 of 20199

  • HighFDA (Devices)·Z-2183-2024·2024-07-03

    Siemens AXIOM MULTIX MP X-ray Tables Recalled for Power Supply Fire Risk

    Siemens Medical Solutions is recalling AXIOM MULTIX MP radiographic X-ray tables due to a potential short circuit in the power supply that may cause overheating and fire. The recall includes 20 units with U.S. nationwide distribution.

    Product
    AXIOM MULTIX MP - Inended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395431
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·24289·2024-07-03

    SWOMOG Children's Two-Piece Pajama Sets Recalled for Burn Hazard

    SWOMOG children's two-piece pajama sets sold on Amazon.com from May 2022 through January 2024 violate federal flammability standards for children's sleepwear, posing a burn hazard. Consumers should stop use immediately and contact SWOMOG for a full refund.

    Product
    SWOMOG Children's Two-Piece Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2204-2024·2024-07-03

    Medtronic Implantable Cardioverter Defibrillator Recalled Due to Weld Crack Defect

    Medtronic is recalling 6 units of the MIRRO MRI VR SureScan implantable cardioverter defibrillator due to a potential manufacturing defect. The devices failed manufacturing quality checks because of a weld crack.

    Product
    MIRRO MRI VR SureScan, Model Number DVME3D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2180-2024·2024-07-03

    X-ray Table Touch Display Power Supply Fire Hazard

    Siemens is recalling AXIOM MULTIX MT X-ray patient tables due to a potential short circuit in the Touch Display power supply that may cause overheating and fire. Fifty units were distributed nationwide.

    Product
    AXIOM MULTIX MT - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395399
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2195-2024·2024-07-03

    Medtronic Implantable Defibrillator Recalled for Manufacturing Weld Defect

    Medtronic recalls 26 units of CROME HF QUAD CRT-D implantable defibrillators worldwide due to weld cracks discovered during manufacturing quality control. Devices were contained before reaching patients.

    Product
    CROME HF QUAD CRT-D MRI SureScan, Model Number DTPC2QQ, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2167-2024·2024-07-03

    FDA Recalls CUSA Excel Surgical Handpiece for Housing Cracks

    Integra LifeSciences is recalling CUSA Excel C2600 surgical handpieces due to potential housing cracks that may delay treatment. The recall affects 2,652 units distributed nationwide and internationally.

    Product
    CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard tissue Catalog Number: C2600* *Note: you may see C2600P or C2600SRL on labeling. This notice is applicable for those SKUs as w
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1428-2024·2024-07-03

    Cream Cheese Stuffed Mini Bagels Recalled for Undeclared Gluten

    FEEL GOOD FOODS INC is recalling Cream Cheese Stuffed Everything Mini Bagels nationwide because the product contains gluten not listed on the label. Consumers with gluten sensitivity should not consume this product.

    Product
    Cream Cheese Stuffed Everything Mini Bagels
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2188-2024·2024-07-03

    Siemens AXIOM Vertix Solitaire Display Fire Risk from Power Supply Short Circuit

    Siemens is recalling the AXIOM Vertix Solitaire diagnostic imaging component due to a short circuit in the Touch Display's power supply unit that may cause overheating and fire. Two units with serial numbers 1239 and 1241 are affected.

    Product
    ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is a component and has been specially designed for examining emergency and accident patients as well as for use in outpatient departments Material Number: 5901900
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2203-2024·2024-07-03

    Implantable Cardioverter Defibrillator Recalled for Manufacturing Weld Defect

    Medtronic recalls 46 PRIMO MRI VR SureScan implantable cardioverter defibrillators due to a manufacturing defect. Weld cracks identified during manufacturing quality checks could cause device failure.

    Product
    PRIMO MRI VR SureScan, Model Number DVMD3D4, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1417-2024·2024-07-03

    Marketside Cinnamon Pecan Braid Recalled for Undeclared Pecan Allergen

    The James Skinner Co. is recalling Marketside Cinnamon Pecan Braid Danish pastry due to incorrect labeling that fails to declare pecans. Consumers with pecan allergies who consume the product could experience allergic reactions.

    Product
    Marketside Cinnamon Pecan Braid, Triple-Filled Danish, Filled with Cinnamon Filling, Topped with Pecans, Sweet Icing and Streusel. Net Wt. 18 oz (1 lb 2 oz) 510g. UPC 7874202922. 6 units per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2194-2024·2024-07-03

    Medtronic COBALT XT Heart Devices Recalled Due to Manufacturing Defect

    Medtronic is recalling 58 COBALT XT HF QUAD implantable cardioverter defibrillators worldwide due to a weld crack manufacturing defect that caused devices to fail quality checks.

    Product
    COBALT XT HF QUAD CRT-D MRI SureScan, Model Number DTPA2QQ, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2212-2024·2024-07-03

    Medtronic Implantable Defibrillators Recalled for Manufacturing Weld Defect

    Medtronic is recalling 82 implantable cardioverter defibrillators due to a manufacturing defect involving weld cracks discovered during quality control testing before distribution to patients.

    Product
    Product not distributed in the US. Implantable Cardioverter Defibrillators: a. VIVA QUAD XT CRT-D, Model Number DTBA2QQ. b. CLARIA MRI CRT-D SureScan, Model Number DTMA2D1. c. CLARIA MRI QUAD CRT-D SureScan, Model Number DTMA2QQ. d. AMPLIA MRI CRT-D SureScan, Mod
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2177-2024·2024-07-03

    Dental Scaler Tip May Not Seat Properly, Posing Injury Risk

    Dental EZ Group is recalling certain Titan Scaler Tip (Perio, Model 261669) units due to an oversized tip holder condition that may prevent proper seating, creating a risk of injury during use.

    Product
    Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of mandibular incisors and deep local pockets.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V208000·2024-07-03

    2022 Keystone Alpine Travel Trailers Recalled for Electrical Fire Risk

    Keystone is recalling 2022 Alpine and related travel trailers due to power inlet lug bolts manufactured too hard to tighten properly, causing loose electrical connections that could lead to fire.

    Product
    KEYSTONE — 2022 KEYSTONE ALPINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2193-2024·2024-07-03

    Implantable Defibrillator Recalled for Manufacturing Weld Crack Defect

    Medtronic is recalling 11 units of the COBALT XT HF QUAD CRT-D MRI SureScan implantable cardioverter defibrillator due to a manufacturing defect involving weld cracks that failed quality control testing.

    Product
    COBALT XT HF QUAD CRT-D MRI SureScan, Model Number DTPA2Q1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2191-2024·2024-07-03

    Medtronic COBALT XT HF CRT-D implantable defibrillator recalled for manufacturing defects

    Medtronic is recalling 8 units of the COBALT XT HF CRT-D MRI SureScan implantable cardioverter defibrillator due to manufacturing defects identified during quality control testing.

    Product
    COBALT XT HF CRT-D MRI SureScan, Model Number: DTPA2D1, Implantable Cardioverter Defibrillator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2182-2024·2024-07-03

    Radiographic X-ray Table Recalled Due to Fire Hazard in Power Supply

    Siemens AXIOM MULTIX MP radiographic X-ray tables are being recalled due to a potential short circuit in the touch display's power supply unit that may cause overheating or fire. 12 units nationwide are affected.

    Product
    AXIOM MULTIX MP - Intended Radiographic X ray Table is a patient table used in conjunction with the Siemens Multix PRO and TOP Systems radiographic devices Material Number: 8395381
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2220-2024·2024-07-03

    CDC Influenza H5 Subtyping Kit may produce inconclusive test results

    The CDC Influenza A/H5 Subtyping Kit's H5b component may fail to amplify, resulting in inconclusive results. 191 units were distributed nationwide.

    Product
    CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2178-2024·2024-07-03

    Sonic Scaler Tip Holder May Be Oversized, Preventing Proper Seating

    The tip holder portion of Titan Blis-Sonic Scaler tips may be oversized, preventing proper seating in the scaler handpiece. This defect could result in the tip becoming loose during use.

    Product
    Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Perio (part number 261669) (1) P/N 264563 (2) P/N 264565 The scaler tip is used with an air drive scaler for subgingival scaling and fine access. The Perio tip is used for lingual supragingival scaling of mandibu
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0569-2024·2024-07-03

    SinuFrin Nasal Decongestant Recalled for Sub-Potency Nationwide

    NeilMed Pharmaceuticals is recalling 20,370 bottles of SinuFrin Quick Relief Decongestant (Lot SD134) nationwide due to sub-potency. No illnesses have been reported.

    Product
    SINUFRIN QUICK RELIEF DECONGESTANT — SINUFRIN QUICK RELIEF DECONGESTANT (SINUFRIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V077000·2024-07-02

    2024 Kia Telluride recalled for engine valve spring failure

    Kia is recalling certain 2024 Telluride vehicles because engine valve springs may break while driving. This could cause loss of drive power and increased risk of fire.

    Product
    KIA — 2024 KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V013000·2024-07-01

    2022 Chevrolet Equinox fuel pump module may cause engine stall

    General Motors is recalling certain 2021-2022 Chevrolet Equinox and 2022 GMC Terrain vehicles because the fuel pump module may not provide sufficient fuel to the engine, causing it to stall and increasing crash risk.

    Product
    CHEVROLET — 2022 CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24744·2024-06-27

    Dania Furniture Recalls Hayden Bookcase Due to Tip-Over Hazard

    Dania Furniture is recalling about 940 Hayden Bookcases sold from November 2017 through February 2024 because the bookcase can tip over and cause entrapment injuries if not anchored to the wall. A 4-year-old child died from a tip-over incident in August 2023.

    Product
    Hayden Bookcase
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24285·2024-06-27

    Brookstone TurboVac Handheld Rechargeable Vacuums Recalled for Fire Hazard

    Southern Telecom is recalling about 10,600 Brookstone TurboVac handheld rechargeable vacuums (Model BSBVAC301) due to a fire hazard caused by battery short circuits during or after charging. The firm has received two reports of serious fires resulting in property damage.

    Product
    Brookstone TurboVac Handheld Rechargeable Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide