The Recall Desk

State

Maryland product recalls

20,364 recalls have nationwide distribution and so reach Maryland. 0 additional recalls listed Maryland specifically in their distribution scope.

About recalls in Maryland

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 Maryland 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.

13726–13750 of 20364

  • ModerateFDA (Drugs)·D-0509-2023·2023-04-12

    Alprazolam 2 mg tablets recalled due to potential manufacturing cross-contamination

    Direct Rx is recalling Alprazolam C-IV 2 mg tablets (NDC 72189-121-60) due to potential cross-contamination at the manufacturer. Nine bottles distributed nationwide; affected lots include 03FE2319 and 13MY2217.

    Product
    Alprazolam C-IV, 2 mg, 60 Tabs per bottle, Rx only, Packaged and Distributed By: Direct Rx Dawsonville, GA 30534, NDC 72189-121-60.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0512-2023·2023-04-12

    Atorvastatin Calcium Tablets 20 mg Recalled Due to Manufacturing Practice Deviations

    Preferred Pharmaceuticals is recalling Atorvastatin Calcium Tablets 20 mg nationwide due to manufacturing practice deviations at the manufacturer, Accord Healthcare, Inc., identified during FDA inspection.

    Product
    Atorvastatin Calcium Tablets, USP, 20 mg, packaged in: a) 90-count bottle (NDC 68788-7631-9); b) 30-count bottle (NDC 68788-7631-3), Rx only, Manufactured: Accord Healthcare, Inc., Durham, NC 27703
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0503-2023·2023-04-12

    Drug Recall: Simvastatin tablets due to manufacturing deviations

    RemedyRepack Inc. is recalling Simvastatin 40 mg tablets nationwide due to manufacturing deviations. The voluntary recall was initiated in March 2023.

    Product
    Simvastatin 40 mg tablets, packaged in a) 30-count bottles (NDC 70518-0060-01) and b) 90-count bottles (NDC 70518-0060-00), Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0499-2023·2023-04-12

    Ropinirole 2mg Tablets Recalled for Manufacturing Practice Deviations

    RemedyRepack Inc. is recalling Ropinirole 2mg tablets due to manufacturing practice deviations. No illnesses have been reported.

    Product
    Ropinirole 2mg tablets, packaged in 180-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC70518-2750-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1319-2023·2023-04-12

    Biosense Webster Guiding Sheath Recalled for Carton Label Mismatch

    Biosense Webster Carto Vizigo Bi-Directional Guiding Sheaths are being recalled because the carton label does not match the inner pouch label. No illnesses or injuries have been reported.

    Product
    Biosense Webster Carto Vizigo Bi-Directional Guiding Sheath, 8.5F(Small), REF D-1385-01-S, RX CE 2797, Sterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0528-2023·2023-04-12

    Cyanocobalamin injection vials recalled for failing potency tests

    Accord Healthcare recalled 4,574 cartons of Cyanocobalamin injection (Lot R2200394) nationwide after testing showed the drug was sub-potent and failed to meet strength specifications.

    Product
    Dodex Injectable Cyanocobalamin Injection, USP 1,000 mcg/mL, 25 x1 ML Multiple dose vials, For Intramuscular or Subcutaneous Use Only, Rx Only, Sterile, Manufactured by: Intas Pharmaceuticals Limited Pharmaz Ahnedabad 382 213, INDIA, Manufactured for: Accord Healthcare, Inc., Dur
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0495-2023·2023-04-12

    Drug Recall: Rosuvastatin 5mg Tablets for Manufacturing Deviations

    RemedyRepack Inc. is recalling 399 bottles of Rosuvastatin 5mg tablets nationwide due to manufacturing deviations. No illnesses have been reported.

    Product
    Rosuvastatin 5mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-3519-00.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0510-2023·2023-04-12

    Montelukast Sodium Oral Granules Recalled for Failed Impurity Specifications

    Teva is recalling Montelukast Sodium Oral Granules 4 mg (lot 3007556A) due to failed impurity specifications. The recall affects 3,772 cartons distributed nationwide.

    Product
    Montelukast Sodium Oral Granules USP, 4 mg, packaged in a carton containing 30 packets, Rx only, Distributed By: Teva Pharmaceuticals USA, Inc., Parsippany, NJ 07054, Carton NDC 0093-7487-56, Packet NDC 0093-7487-19
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0497-2023·2023-04-12

    Drug Recall: Tadalafil 5 mg Tablets Due to Manufacturing Deviations

    RemedyRepack Inc. recalled Tadalafil 5 mg tablets due to cGMP manufacturing process deviations. The recall affected 16 bottles distributed nationwide; no illnesses have been reported.

    Product
    Tadalafil 5 mg tablets, 30-count bottles, Rx only, Repackaged by: RemedyRepack Inc., Indiana, PA 15701, NDC 70518-2972-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0526-2023·2023-04-12

    Prescription Tadalafil tablets recalled for manufacturing process deviations

    Preferred Pharmaceuticals is recalling 32 bottles of Tadalafil 20 mg tablets due to manufacturing process deviations identified during FDA inspection. The recalled lots expire January 31, 2024.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·23V672000·2023-04-10

    2023 Harley-Davidson FLTRXSE Motorcycles Recalled for Brake Line Defect

    Harley-Davidson is recalling 2023 FLTRXSE and FLHXSE motorcycles due to improperly secured rear brake line clamps. The brake line may chafe against the exhaust pipe, causing fluid leaks that reduce braking ability.

    Product
    HARLEY-DAVIDSON — 2023 HARLEY-DAVIDSON FLTRXSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V842000·2023-04-10

    2021 Dodge Durango Rear Spoiler May Detach, Becoming Road Hazard

    Chrysler is recalling 2021 Dodge Durango vehicles because the rear spoiler may not be properly aligned and could detach during liftgate use, creating a road hazard. Dealers will replace the spoiler free of charge.

    Product
    DODGE — 2021 DODGE DURANGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V753000·2023-04-09

    Tiffin Wayfarer RV Water Tank Mounting Defect Increases Crash Risk

    Tiffin Motorhomes is recalling 2018-2022 Wayfarer RVs because the rear water tank mounting bolts can fail, causing the tank to fall onto the exhaust pipe. This affects vehicle stability and increases crash risk.

    Product
    TIFFIN — 2018 TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V694000·2023-04-09

    Coachmen motorhomes recalled for improperly tightened LPG quick disconnect

    Forest River is recalling certain 2022-2023 Coachmen Leprechaun, Freelander, and Prism motorhomes due to an improperly tightened auxiliary LPG quick disconnect that could cause a gas leak and increase fire risk.

    Product
    COACHMEN — 2022 COACHMEN LEPRECHAUN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V755000·2023-04-09

    2022 Thor Motor Coach Rize Motorhomes Recalled for LP Gas Line Rupture Risk

    Thor Motor Coach is recalling 2022 Rize and Scope motorhomes due to an LP gas line that may be too short and improperly installed. A gas leak from a ruptured line could cause a fire.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH RIZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V754000·2023-04-09

    Thor Motor Coach Omni motorhomes recalled for LP gas line fire hazard

    Thor Motor Coach is recalling 2021-2022 Omni and Magnitude motorhomes due to an LP gas line routing defect. The line may be incorrectly routed through the rear suspension leaf springs, potentially causing a gas leak and fire risk.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V696000·2023-04-09

    Winnebago Travato motorhomes recalled for unintended awning extension

    Winnebago is recalling certain 2019-2023 Travato motorhomes because the retractable awning may extend unintentionally during transit. An extended awning could become a distraction or road hazard, increasing crash risk.

    Product
    WINNEBAGO — 2019 WINNEBAGO TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V695000·2023-04-09

    Motorhome Retractable Awning Unintended Extension During Transit Recall

    Winnebago and Itasca motorhomes have a defective retractable awning that may extend unintentionally while driving. This can distract drivers or create a road hazard, potentially increasing crash risk.

    Product
    ITASCA — 2023 ITASCA NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V767000·2023-04-09

    Entegra Class A Motorhomes Recalled for Fuel Hose Leak Fire Risk

    Entegra Coach is recalling certain 2021-2022 Anthem, Aspire, and Reatta XL Class A motorhomes with Cummins diesel engines due to fuel hoses that may leak and pose a fire risk. Owners should contact Entegra customer service at 1-800-283-8267 for free replacement.

    Product
    ENTEGRA — 2021 ENTEGRA ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V556000·2023-04-08

    2024 Hyundai Tucson Recalled for Incorrect Tire Information Label

    The tire and loading information label on 2024 Hyundai Tucson vehicles may provide incorrect spare tire information, potentially causing confusion during emergency tire replacement.

    Product
    HYUNDAI — 2024 HYUNDAI TUCSON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V551000·2023-04-08

    2024 Subaru Impreza harness short circuit may cause loss of drive power

    Subaru is recalling certain 2024 Impreza and Crosstrek vehicles because the instrument panel harness may contact the steering beam bracket, causing electrical short circuits that could lead to loss of drive power and increased crash risk.

    Product
    SUBARU — 2024 SUBARU IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V557000·2023-04-08

    2023 Genesis GV60 Seat Belt Retractor May Fail to Fasten Properly

    Hyundai is recalling certain 2023 Genesis GV60 vehicles because the automatic locking retractor for the front passenger-side seat belt may fail to fasten or extend properly, preventing adequate occupant restraint in a crash.

    Product
    GENESIS — 2023 GENESIS GV60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V577000·2023-04-07

    2022 Kia Telluride Instrument Cluster Display May Go Blank

    Certain 2022 Kia Telluride vehicles have instrument cluster displays that may go blank after startup, potentially hiding critical driving information like speed and gear selection. Kia will update the software at no cost.

    Product
    KIA — 2022 KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23174·2023-04-06

    Mammut Avalanche Shovels Recalled for Spring Locking Mechanism Failure

    Mammut Sports Group is recalling Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels because the spring locking mechanism can fail during emergency excavation, posing risk of injury or death.

    Product
    Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V429000·2023-04-06

    2023 IC CE School Bus Steering Gear May Fracture, Causing Loss of Control

    Navistar is recalling certain 2022-2023 IC CE School Buses because their steering gears may have been assembled incorrectly and could fracture, causing a loss of steering control and increasing crash risk.

    Product
    IC BUS — 2023 IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide