The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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14426–14450 of 31492

  • HighFDA (Devices)·Z-1314-2024·2024-03-27

    Abbott Point of Care Control Device Recalled Due to Temperature Storage Failure

    Abbott's i-STAT Level 1 control device is recalled because a refrigerator temperature excursion on January 8, 2024, could cause incorrect or delayed test results. The walk-in storage unit failed, causing temperatures to fall below the required range of 35.6-46.4°F.

    Product
    Abbott Point of Care Control Control i-STAT¿ Level 1 10 X 1.7 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1329-2024·2024-03-27

    Hip Traction Boot Assembly Defect Could Cause Device Detachment

    Baxter Healthcare is recalling HDS Traction Boot II units due to incorrect assembly. The boot key socket locking ridge faces upward, preventing proper attachment to the traction system.

    Product
    HDS Traction Boot II, REF AR-6529-23, The Traction Boot is designed to position, support and/or distract the patient's foot for hip surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1348-2024·2024-03-27

    Guidewire Introducer Sheath Recalled for Internal Lumen Voids

    Angiodynamics is recalling 39 units of MINI STICK MAX vascular guidewire introducers due to voids in the sheath hub that may prevent guidewire passage during surgery, potentially delaying the procedure.

    Product
    MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. - Catalog Number: 45-781
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1341-2024·2024-03-27

    Angiodynamics Guidewire Introducer Recall Due to Manufacturing Defect

    Angiodynamics recalls approximately 5,840 guidewire introducers with manufacturing defects that may prevent proper guidewire insertion during vascular procedures. The defect could cause procedural delays requiring equipment exchange.

    Product
    MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1317-2024·2024-03-27

    Medtronic Abre Venous Stent System Recalled for Sterile Package Breach

    Medtronic is recalling Abre Venous Self-expanding Stent Systems due to a potential for sterile package breach. The recalled systems consist of three product numbers totaling 65 units distributed worldwide. No injuries have been reported.

    Product
    Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1343-2024·2024-03-27

    Vascular Guidewire Introducer Sheath Recalled for Internal Hub Defect

    Angiodynamics recalls 130 MINI STICK MAX guidewire introducers due to hub voids that may prevent guidewire passage during vascular procedures. No injuries reported.

    Product
    MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-765
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1309-2024·2024-03-27

    Nautilus ECMO Oxygenator recalled due to heat exchanger water path restriction

    Mc3 Inc recalls Nautilus ECMO Oxygenator units due to heat exchanger water path restriction that degrades temperature control performance. Inadequate heat transfer may lead to hypothermia risk.

    Product
    NautilusTM ECMO Oxygenator with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: (1) 48145; (2) 48145E
    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
  • HighFDA (Food)·F-1084-2024·2024-03-27

    Ethos Bakery Vegan Snickerdoodles Recalled for Undeclared Wheat Allergen

    Ethos Bakery is recalling 4 oz packages of Vegan Snickerdoodles distributed in Washington because the labels do not clearly specify that wheat flour is present, creating a risk for consumers with wheat allergies.

    Product
    Vegan Snickerdoodle; 4 oz/plastic sleeve; The label of recalled product is read in parts: ***Vegan Snickerdoodle ***[Ingredients: Granulated sugar, Wheat flour, Vegan butter (refined coconut oil, soy milk, vegetable oil, soy lecithin,) Sonoran wheat flour, Water, Egg replacer (
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1319-2024·2024-03-27

    I.B.S. 6.5-C Compression Screw Batch Recalled for Dimensional Mix-Up

    A batch of I.B.S compression screws may have incorrect dimensions compared to their labels due to a batch mix-up. The 59 affected units were distributed nationwide in Tennessee.

    Product
    I.B.S¿ 6.5-C Compression screw - diam 6.5mm lg 75mm,Part Number S65 ST175
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1331-2024·2024-03-27

    Directional Laser Probe Recalled for Fiber Extension and Direction Difficulties

    D.O.R.C. Dutch Ophthalmic Research Center is recalling Directional Laser Probes for ophthalmic surgery due to difficulties extending, retracting, and directing the laser fiber. The recall affects 84 units distributed nationwide.

    Product
    Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1304-2024·2024-03-27

    Siemens DCA HbA1c Reagent Kit Recalled for Inaccurate Test Results

    Siemens is recalling its DCA HbA1c Reagent Kit because the device displays falsely elevated readings without alerting the user. This could lead to incorrect patient management of glucose levels.

    Product
    DCA Systems HbA1c Reagent Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1340-2024·2024-03-27

    Vascular Guidewire Introducer Recalled Due to Internal Hub Defect

    A vascular guidewire introducer is recalled because internal voids in the hub may prevent proper guidewire passage, potentially delaying surgical procedures.

    Product
    MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-758
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1322-2024·2024-03-27

    Dental Implant Impression Coping Recalled for Manufacturing Defect

    Thommen Medical AG is recalling impression coping units because the internal canal depth was not manufactured according to specifications, preventing firm connection to the dental implant. The product was distributed in Ohio and Kentucky.

    Product
    impression coping, repositionable, short, screw-retained, PF 4.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1318-2024·2024-03-27

    TMINI Knee Instrument Array Guide May Bind During Surgical Drilling

    A precision component in Think Surgical's TMINI robotic knee system may bind due to insufficient clearance. The binding could occur during surgical drilling.

    Product
    Assembly, Array Guide TMINI, REF: 109101, part of the TMINI Knee Instrument Set, used with the TMINI Miniature Robotic System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1083-2024·2024-03-27

    Vegan Pecan Oat Scones Recalled for Undeclared Wheat Allergen

    Ethos Bakery is recalling Vegan Pecan Oat Scones distributed in Washington because the product label fails to declare wheat as an allergen, despite wheat flour being present in the product.

    Product
    Vegan Pecan Oat Scone; 4 oz/plastic sleeve; The label of recalled product is read in parts: [Ingredients: Granulated sugar, Wheat flour, Vegan butter (refined coconut oil, soy milk, vegetable oil, soy lecithin,) Sonoran wheat flour, Water, Egg replacer (potato starch, tapioca
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1350-2024·2024-03-27

    Convatec EsteemBody Drainable Pouches Recalled for Filter Weld Defect

    ConvaTec is recalling specific lots of EsteemBody Soft Convex Drainable Pouches due to inconsistency in filter weld strength, affecting 6709 units distributed in the US and internationally.

    Product
    Convatec EsteemBody Soft Convex, Drainable Pouch, Product codes (REF): a) 423643, b) 423658, c) 423659, d) 423664, e) 423666, f) 423645, g) 423667, h) 423657, i) 423652, j) 423646, k) 423654, l) 423653, m) 423647, n) 423644, o) 423648, p) 423665, q) 423656, r) 423651, s) 423660,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1081-2024·2024-03-27

    Bread Butter White Bread Recalled Due to Foreign Material Contamination

    Albertsons is recalling Signature Select, Athens, and Cal Pia brand Bread Butter White Bread due to possible metal and plastic shavings in the product. The recall affects approximately 13,550 units distributed in California and Nevada.

    Product
    Signature Select, Athens, and Cal Pia brand Bread Butter White Bread 22 oz. loaf
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1092-2024·2024-03-27

    Ground Cinnamon Product Recalled Due to Elevated Lead Levels

    El Chilar ground cinnamon (1.25 oz bags) is being recalled due to elevated levels of lead. Affected products were distributed in Maryland; consumers should not use them.

    Product
    El Chilar, Canela Molida, Ground Cinnamon NET WT. 1.25 Oz (35g) , BOPP Bag, 12 units per cases
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1310-2024·2024-03-27

    ECMO heat exchanger module recalled due to water path restriction

    Mc3 Inc is recalling 188 Nautilus Smart ECMO modules nationwide due to potential water path restrictions in the heat exchanger that may cause inadequate heat transfer and risk of hypothermia during use.

    Product
    NautilusTM Smart ECMO Module with Balance Biosurface-used in extracorporeal life support procedures to oxygenate blood, remove carbon dioxide and regulate blood temperature. Product Number: 48135, 48135E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1075-2024·2024-03-27

    Dole Premium Kit Endless Summer Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Dole Premium Kit Endless Summer salad kits due to potential Listeria monocytogenes contamination. Affected products have specific production codes dated February 2024.

    Product
    Dole Premium Kit Endless Summer UPC 71430010730
    Category
    Food
    Distribution
    25 states
  • HighFDA (Devices)·Z-1308-2024·2024-03-27

    Curaplex Nasal Intubation Kit with incompatible tube holder recalled

    Sarnova HC is recalling the Curaplex Nasal Intubation Kit because the endotracheal tube holder is incompatible with nasal intubation, preventing practitioners from securing the tube. The recall affects 550 units distributed nationwide.

    Product
    Curaplex Nasal Intubation Kit w/ 7mm Endotracheal Tube-To perform a nasal intubation to establish an airway in an emergency. Item Number: 023070S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1330-2024·2024-03-27

    Laparotomy Sponges recalled for incomplete sterilization and missing RF detection

    Covidien is recalling Situate Laparotomy Sponges because some packs may contain improperly sterilized units lacking required RF detection features. Non-sterile sponges could cause infection, tissue trauma, and sepsis during surgery.

    Product
    Situate Laparotomy Sponge, RF and X-ray Detectable, REF: L1818-04P01C-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1321-2024·2024-03-27

    Preat Nobel RP Titanium Abutment Blank Recalled for Manufacturing Defect

    Preat Corp is recalling 561 units of RP Titanium Abutment Blanks due to a manufacturing defect where the screw seat location may be too high, resulting in shortened screw engagement into the implant.

    Product
    Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1312-2024·2024-03-27

    Pregnancy Test Control Set Recalled for Temperature Excursion Risk

    McKesson recalls Abbott Rapid Dx pregnancy test control sets due to a refrigerator temperature excursion that could cause inaccurate or delayed test results.

    Product
    Abbott Rapid Dx N America LLC Reproductive Endocrinology Control Set McKesson Consult" Pregnancy (hCG) Testing Positive Level / Negative Level 2 X 4 mL
    Category
    Medical Device
    Distribution
    Distributed nationwide