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 the agency’s own highest classification or reported deaths or serious injuries, 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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14401–14425 of 89769

  • HighFDA (Devices)·Z-1167-2024·2024-02-28

    ESG Cutting Forceps Jaw May Fracture During Use or Inspection

    Olympus Corporation of the Americas is recalling ESG PK Cutting Forceps because the jaw may fracture during pre-procedure inspection or during the procedure, posing a potential injury risk.

    Product
    ESG PK CUTTING FORCEPS, 5MM, 33CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0347-2024·2024-02-28

    Drug recall: CABTREO topical gel stored at improper temperature

    CABTREO acne medication was stored outside refrigeration requirements. The recalled lot was kept at room temperature instead of required refrigerated conditions.

    Product
    CABTREO — CABTREO (CLINDAMYCIN PHOSPHATE/BENZOYL PEROXIDE/ADAPALENE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1152-2024·2024-02-28

    Philips Azurion X-ray Systems Disk Bay May Fail and Prevent Imaging

    The disk bay component in certain Philips Azurion x-ray systems may fail, potentially preventing diagnostic imaging and delaying procedures. Affected units have been distributed worldwide.

    Product
    Philips Azurion Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of the affected system. Affected PCs: XRay PC, Suite PC, and FlexViewing PC Azurion Model Name - Model Number: Azurion 3 M12 722063 722221; Azurion 3 M15 722064…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0336-2024·2024-02-28

    Intravenous norepinephrine drug recalled for incorrect concentration labeling

    Baxter Healthcare is recalling 13,000 bags of norepinephrine bitartrate injection due to an overwrap label incorrectly showing 4 mg/250 mL concentration, while the primary bag label correctly shows the actual 8 mg/250 mL strength.

    Product
    NOREPINEPHRINE BITARTRATE — NOREPINEPHRINE BITARTRATE (NOREPINEPHRINE BITARTRATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0329-2024·2024-02-28

    Meijer Cherry Cough Drops recalled for potential glass and silicone contamination

    Bestco LLC is recalling Meijer Cherry Cough Drops due to potential glass and silicone particulates found during manufacturing quality control inspections. Consumers should stop using the product immediately.

    Product
    Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000345, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0342-2024·2024-02-28

    Adrenalin Epinephrine Injection Recalled Due to Incorrect Expiration Date Label

    Henry Schein Inc. and Glove Club HSI Gloves Inc. are recalling 1,099 vials of Adrenalin (Epinephrine) Injection because the expiration date on the repack pouch label is incorrect. The product was distributed nationwide.

    Product
    ADRENALIN — ADRENALIN (EPINEPHRINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0332-2024·2024-02-28

    Equate Cherry Cough Drops recalled for potential glass and silicone contamination

    Bestco LLC is recalling Equate Cherry Cough Drops nationwide due to potential glass and silicone particulates from manufacturing deviations. Affected products are 30-drop and 160-drop bags expiring December 31, 2026.

    Product
    Equate Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, a) 30 drops per bag, item number 20000462, b) 160 drops per bag, item number 20000463, Bestco, 288 Mazeppa Road, Mooresville, NC 28115
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1153-2024·2024-02-28

    EndoVive Replacement Button Kits mislabeled with incorrect sizing

    Boston Scientific is recalling EndoVive Replacement Button Kits due to sizing mislabeling that could cause undersizing and serious complications including tissue damage and sepsis.

    Product
    EndoVive Replacement Button Kit w/ ENFIT 28F 2.8 CM, Outer Box UPN M00509500 or M00509510.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1170-2024·2024-02-28

    3M Surgical Clipper Blade Assembly Recalled Due to Burn Risk

    3M recalled 764,580 Specialty Blade Assemblies for surgical clippers due to risk of burns from overheating. The blade can reach temperatures exceeding 77°C if left running improperly.

    Product
    3M Specialty Blade Assembly, REF 9660,70-2011-8491-1, 7100213026, used with used with 3M Surgical Clipper Catalog Number 9661L
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1175-2024·2024-02-28

    Automated Impella Controller Software Update Resolves Pump Recognition Issue

    Abiomed is releasing software Version 8.5 for the Automated Impella Controller to fix an issue in versions 8.4 and 8.4.1 where the device failed to recognize the pump. Approximately 4,463 units were distributed nationwide.

    Product
    Automated Impella Controller (AIC), Product No. 0042-0000-US, 0042-0010-US, 0042-0040-US. Used with Impella Ventricular Support Systems (cardiovascular)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0880-2024·2024-02-28

    Flour recalled for potential metal and foreign material contamination

    Mennel Milling Company is recalling flour products due to potential contamination with metal, wood, gasket material, and sifter balls. Affected product was distributed in Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    160919 FLR BLE WINTER delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1155-2024·2024-02-28

    X-ray fluoroscopy system may display abnormal images due to detector board defect

    Canon Medical's INFX-8000F X-ray system may display abnormal horizontal stripe patterns due to a manufacturing change in the flat panel detector's internal board, potentially preventing exam completion.

    Product
    The INFX-8000F is designed to take advantage of the latest technological innovations to reduce dose and to save time. A revolutionary graphic user interface and a multi-tasking computer enable the system to fully meet the requirement for optimum image quality, safety, ease of…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0902-2024·2024-02-28

    Pizza 50/50 Flour Recalled for Potential Metal, Wood, and Foreign Material

    Mennel Milling Company recalls Pizza 50/50 Unmalted flour due to potential metal, wood, gasket material, and sifter ball contamination. The affected product was distributed across KY, MI, NJ, NY, and PA.

    Product
    PIZZA 50/50 UNMALTED 904181 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0915-2024·2024-02-28

    Country Corner Dairy Sizzling Colby Cheese Recalled Due to Improper Pasteurization

    Country Corner Dairy is recalling Sizzling Colby Cheese due to lack of proper pasteurization. The recalled product was distributed in Maryland and Virginia.

    Product
    Fresh Local , Country Corner Dairy, SIZZLING COLBY CHEESE, INGREDIENTS: Pasteurized Milk, Salt , Rennet, Calcium Chloride, Cheese Culture, Peppers, Contains Milk. Product comes in various sizes, 6 oz. up to 42 lbs. and is in vacuum sealed plastic packaging.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0892-2024·2024-02-28

    Flour Product Recall Due to Foreign Material Contamination

    Mennel Milling Company is recalling 2.6 million pounds of bulk AP flour that may contain metal, wood, gasket material, and sifter balls. The flour was distributed in six states and should not be used.

    Product
    01050 KA AP FLOUR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighUSDA FSIS·008-2024·2024-02-28

    M&P Production Recalls Raw Lamb and Beef Samsa for Undeclared Sesame

    M&P Production LTD is recalling raw lamb and beef samsa products because they contain sesame seeds, a known allergen, that are not declared on the label.

    Product
    M&P Production LTD — M&P Production LTD Recalls Raw Lamb and Beef Samsa Products Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·24V157000·2024-02-28

    Commercial truck camera cable routing can damage wiring and cause fire

    Isuzu is recalling certain FTR, FVR and Chevrolet LCF trucks with Mobileye Collision Warning Systems because a misrouted camera cable can damage wiring and overload the electrical circuit.

    Product
    CHEVROLET — CHEVROLET, ISUZU 7500XD, 6500XD, FTR, FVR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1156-2024·2024-02-28

    Philips Allura Xper X-ray System Memory Modules May Stop Functioning

    Philips Allura Xper fluoroscopic X-ray systems may experience memory module failures that cause the system to stop functioning and prevent imaging. This malfunction could delay critical medical procedures.

    Product
    Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs (Dual In-line Memory Modules) used with affected systems. Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10/10 722005 722011 722027…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0879-2024·2024-02-28

    Flour Recalled for Potential Foreign Material Contamination

    Mennel Milling Company is recalling approximately 2.6 million pounds of ALL PURPOSE EN EZ BL flour due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    15953 ALL PURPOSE EN EZ BL delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0887-2024·2024-02-28

    Pizza 50/50 Unmalted Flour Recalled for Potential Foreign Material

    Mennel Milling Company is recalling approximately 2.6 million pounds of PIZZA 50/50 UNMALTED flour due to potential contamination with metal, wood, gasket material, and sifter balls.

    Product
    PIZZA 50/50 UNMALTED delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0899-2024·2024-02-28

    Mennel Milling I-52 Patent Flour Recalled for Foreign Material Contamination

    Mennel Milling Company recalled I-52 Patent Flour containing potential foreign material including metal, wood, gasket material, and sifter balls. The flour was distributed in bulk trailers across six states.

    Product
    I-52 PATENT FLOUR delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0895-2024·2024-02-28

    FDA Recalls Bulk Milling Product for Potential Foreign Material

    Mennel Milling Company is recalling its milling product (2-15969-0000) due to potential contamination with metal, wood, gasket material, and sifter balls. The product was distributed across Kentucky, Michigan, New Jersey, New York, Ohio, and Pennsylvania.

    Product
    2-15969-0000 delivered as bulk product in approximately 50,000 lbs trailers
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1176-2024·2024-02-28

    Philips Azurion 3 Surgical Imaging System Recalled for Power Failure Risk

    Philips is recalling 14 units of its Azurion 3 surgical imaging system due to a potential short circuit in the power inverter. The defect could cause the device to lose power and fail during surgical procedures.

    Product
    Azurion 3 with a Certeray generator -To perform image guidance in diagnostic, interventional, and minimally invasive surgery procedures Models: (1) 722221 (2) 722222 (3) 722280
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0337-2024·2024-02-28

    Voriconazole Oral Suspension Recalled for Missing Package Insert

    Lupin Pharmaceuticals recalls Voriconazole for Oral Suspension (40mg/mL) due to missing or incorrect package inserts on affected batches distributed in Ohio, Illinois, and New Jersey.

    Product
    VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
    Category
    Drug
    Distribution
    3 states
  • SevereNHTSA·24V152000·2024-02-27

    Toyota Tacoma Recall: Rear Axle Shaft Separation Risk

    Toyota is recalling certain 2022-2023 Tacoma trucks because the rear axle shaft may separate from the axle housing due to debris causing improperly secured fasteners, increasing the risk of a crash.

    Product
    TOYOTA — TOYOTA TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide