The Recall Desk

State

Maryland product recalls

73,187 recalls have nationwide distribution and so reach Maryland. 8,223 additional recalls listed Maryland specifically in their distribution scope.

What the numbers show

Total
8,223
Critical
996
Severe
2,134
Most recent
2026-09-25

Of the 8,223 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,134 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,223 recalls whose distribution notice names Maryland specifically. The 73,187 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13076–13100 of 81410

  • CriticalFDA (Food)·F-1082-2024·2024-03-27

    Stonewall Kitchen Gluten Free Doughnut Mix Recalled for Undeclared Wheat

    Stonewall Kitchen is recalling Cinnamon Sugar Doughnut Mix (Gluten Free) with use-by dates of March 9-10, 2025, because units contain undeclared wheat. Consumers with wheat allergies or celiac disease should not consume this product.

    Product
    Stonewall Kitchen Cinnamon Sugar Doughnut Mix; Gluten Free; Home-Baked & Gluten Free; Net Wt. 18oz (510g); UPC: 1138131332
    Category
    Food
    Distribution
    44 states
  • CriticalFDA (Food)·F-1089-2024·2024-03-27

    HEB Poblano Caesar Dressing recalled for Listeria monocytogenes contamination

    Reser's Fine Foods is recalling HEB Poblano Caesar Dressing due to Listeria monocytogenes contamination from repackaged Cotija cheese. The recall affects 2495 cases distributed across 16 states.

    Product
    FCF Item 403953, HEB Poblano Caesar Dressing, 12oz. glass bottle, 6 bottles per case. UPC 41220 94807
    Category
    Food
    Distribution
    16 states
  • CriticalFDA (Food)·F-1087-2024·2024-03-27

    Don Pancho Fiesta Sauces Recalled for Listeria Monocytogenes Contamination

    Reser's Fine Foods is recalling Don Pancho Fiesta 3 Pack Everything Sauce due to potential Listeria monocytogenes contamination from recalled Cotija cheese repackaged into these ready-to-eat products.

    Product
    Item # 407034, Don Pancho Fiesta 3 Pack Everything Sauce. Each pack consists of Cilantro Lime Crema, Baja-Style Crema, Chipotle Crema. 3/12oz glass bottles per pack, 6 packs per case. UPC on 3-pack box: 0 71117 00741 1.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1090-2024·2024-03-27

    Costco Southwest Wrap Kit Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Costco Southwest Wrap Kits due to Listeria monocytogenes contamination. The product was distributed across 16 states.

    Product
    FCF Item 406957, Costco Item # 1744097, Club COSTCO SW Wrap Kit, Costco Service Deli, 2/8.15 lbs. Net Wt. 16.31 lbs., UPC 0 13454 38424 4. Costco assembled and sold product as Southwest Wrap with Sauce, item #29433.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1072-2024·2024-03-27

    Dole Chopped Kit Avocado Ranch Recalled for Potential Listeria Contamination

    Dole Chopped Kit Avocado Ranch (UPC 71430000915) is being recalled due to potential contamination with Listeria monocytogenes. The FDA Class I recall affects 50,645 cases distributed across the United States and Canada.

    Product
    Dole Chopped Kit Avocado Ranch UPC 71430000915
    Category
    Food
    Distribution
    25 states
  • SevereNHTSA·24V233000·2024-03-27

    2025 Peterbilt and Kenworth Trucks Recalled Over Steering Gear Defect

    PACCAR is recalling certain 2025 Peterbilt and Kenworth trucks because the steering gear sector shaft may have been improperly heat-treated, which can cause the gear teeth to crack or fracture.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, T680, T280, T380
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1074-2024·2024-03-27

    Dole Cajun Ranch Chopped Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables is recalling 50,645 cases of Dole Cajun Ranch Chopped Kit UPC 71430002063 due to potential Listeria monocytogenes contamination. The affected product was distributed in 24 U.S. states and Canada.

    Product
    Dole Cajun Ranch Chopped Kit UPC 71430002063
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Devices)·Z-1300-2024·2024-03-27

    FDA Recalls HeartMate II Left Ventricular Assist Systems for Graft Obstruction

    Thoratec Corp. recalls HeartMate II left ventricular assist system kits due to outflow graft deformation that could obstruct blood flow. The FDA has classified this as a Class I recall affecting 2,240 units distributed worldwide.

    Product
    HeartMate II Left Ventricular Assist System (LVAS): 1. HeartMate II Sealed Outflow Graft with Bend Relief REF 103393 2. HeartMate II LVAS Implant Kit, US REF 106015 3. HeartMate II LVAS Implant Kit, OUS REF 106016 Update (February 14, 2024) HeartMate II Left Ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V236000·2024-03-27

    Heartland RV Cooktop LED Backlight Circuit Fire Risk Recall

    Heartland is recalling 10,038 model year 2023-2024 fifth wheels and travel trailers because the LED backlight circuit board in the cooktop range may fail and overheat, increasing the risk of a fire.

    Product
    HEARTLAND — HEARTLAND PROWLER, SOUTH FORK, SUNDANCE, MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0393-2024·2024-03-27

    FDA Recalls Unapproved Tianeptine Elixir Drug Product Nationwide

    Neptune's Fix Tianeptine Elixir, distributed nationwide by Super Chill Products, is recalled because it contains tianeptine, a substance not approved by the FDA for any medical use in the United States. Consumers should not use this product.

    Product
    Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl.oz. (10 mL) bottle, Distributed By Superchill Products, 827 6th Avenue, New York, New York 10001.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1088-2024·2024-03-27

    HEB Cilantro Cotija Dressing recalled due to Listeria contamination

    Reser's Fine Foods is recalling HEB Cilantro Cotija Dressing due to potential Listeria monocytogenes contamination. The dressing was distributed across multiple states in approximately 5,589 cases.

    Product
    FCF Item 403949, HEB Cilantro Cotija Dressing Perfect for Tacos, 12oz glass bottle, 6 bottles per case. UPC on bottle: 41220 94799.
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Devices)·Z-1301-2024·2024-03-27

    HeartMate 3 Left Ventricular Assist System recalled for outflow graft obstruction

    The FDA is recalling the HeartMate 3 Left Ventricular Assist System due to observed outflow graft deformation that can obstruct blood flow. Patients with implanted devices should contact their healthcare provider.

    Product
    HeartMate 3 Left Ventricular Assist System (LVAS): 1. HeartMate 3 Sealed Outflow Graft with Bend Relief, Investigational Device Exemption (IDE) 2. HeartMate 3 Sealed Outflow Graft with Bend Relief, US 3. HeartMate 3 Sealed Outflow Graft with Bend Relief, OUS 4. HeartMate 3…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1086-2024·2024-03-27

    Cilantro Lime Crema Products Recalled for Listeria Contamination

    Reser's Fine Foods is recalling Cilantro Lime Crema products sold under Costco and Don Pancho labels due to Listeria monocytogenes contamination. Products were distributed across 16 states.

    Product
    FCF Item #404967, Costco Item #1506878, Cilantro Lime Crema, 60/4oz plastic cups per case. Labeled cups only sold in bulk for Food Service Use not for individual sale. UPC 13454 38195. FCF Item #404689, Don Pancho Cilantro Lime Crema Everything Sauce, 32oz glass bottle, sold as…
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Food)·F-1076-2024·2024-03-27

    Marketside Chopped Salad Kit Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Marketside Chopped Salad Kit Bacon Crunch due to potential Listeria monocytogenes contamination. Affected packages have lot codes B020-B036 with production dates from February 5, 2024 through February 21, 2024.

    Product
    Marketside Chopped Salad Kit Bacon Crunch UPC 681131305440
    Category
    Food
    Distribution
    25 states
  • SevereNHTSA·24V235000·2024-03-27

    Cruiser RV Recalls Travel Trailers Due to Cooktop Fire Risk

    Cruiser RV is recalling 2023-2024 travel trailers and fifth wheels because a faulty LED circuit board in the cooktop may overheat and cause a fire.

    Product
    CRUISER — CRUISER, CRUISER RV MPG, STRYKER, TWILIGHT, AVENIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1267-2024·2024-03-27

    ARROW QuickFlash Radial Artery Catheters Recalled for Defective Component

    ARROW International is recalling 1,160,470 QuickFlash radial artery catheterization devices due to a defective guidewire handle that can cause arterial vasospasm and vessel injury.

    Product
    ARROW QuickFlash Radial Artery Catherization (wire, guide, catheter), Part Numbers: a) REF AK-04220; b) REF ASK-04220-FMH1; c) REF ASK-04220-HHC; d) REF ASK-04220-KSP; e) REF ASK-04220-PSU; f) REF ASK-04220-UCL1; g) REF ASK-04500-AH; h) REF ASK-04500-HF-S; i)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V234000·2024-03-27

    Keystone RV Company Recalls Certain RV Models Due to Cooktop Fire Risk

    Keystone RV Company is recalling various 2021-2024 RV models because the cooktop LED backlight circuit board may overheat and increase the risk of fire.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN, CROSSROADS FUZION, MONTANA, ASPEN TRAIL, MONTANA HIGH COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1274-2024·2024-03-27

    Smiths Medical Pneupac paraPAC plus 310 ventilators recalled for malfunction

    Smiths Medical is recalling paraPAC plus 310 ventilators that may malfunction by delivering continuous gas flow instead of cycling breaths. The defect affects 10,140 units distributed worldwide and prevents proper ventilation.

    Product
    smiths medical Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1091-2024·2024-03-27

    Chicken Taco Kits Recalled for Listeria Contamination Risk

    Reser's Fine Foods is recalling multiple chicken taco kits distributed across 16 states due to potential Listeria monocytogenes contamination in a repackaged cheese ingredient. Consumers should not consume affected products.

    Product
    Item 404764, KIT EM CHICKEN STREET TACO DP EXPRESS MEAL 6/22 OZ, UPC 7111712500. The following Taco Kits were distributed to consignees with instructions for assembly at retail store kitchen: Item 406987, KIT OP CHICKEN TACO MINI SINGLE SERVE ON PREMISE NO TRAYS 2/2.4925 LB…
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Devices)·Z-1275-2024·2024-03-27

    Smiths Medical Pneupac Plus 300 Ventilator Cycling Malfunction

    Smiths Medical Pneupac Plus 300 ventilators may intermittently deliver continuous airflow instead of cycling breaths as designed. This malfunction affects 2,902 units distributed worldwide.

    Product
    smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1320-2024·2024-03-27

    Medical Device Recall: Orthopedic Compression Screws with Incorrect Dimensions

    In2Bones, SAS is recalling I.B.S Compression screws due to a batch mix-up. Affected screws may have different lengths than indicated on their labels, creating a risk of improper surgical implantation.

    Product
    I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 80mm,Part Number S65 ST180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1342-2024·2024-03-27

    Surgical Guidewire Introducer Sheath Recalled for Internal Manufacturing Defects

    Angiodynamics vascular guidewire introducers (600 units) may have internal defects preventing proper function during surgery. Defects could cause procedure delays and require device exchange.

    Product
    MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-762
    Category
    Medical Device
    Distribution
    Distributed nationwide