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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5101–5125 of 36541

  • SevereFDA (Devices)·Z-0035-2024·2023-10-18

    Hemodialysis Systems Recalled for Potential PCBA Tubing Leaching

    Fresenius Medical Care is recalling 733 hemodialysis machines nationwide due to potential leaching of circuit board material from tubing. Affected equipment may contaminate blood or dialysate during treatment.

    Product
    2008T HD SYS. W/O CDX W/BIBAG BLUESTAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0007-2024·2023-10-18

    LuLu Chinese Express Korean Noodles Recalled for Undeclared Egg Allergen

    LuLu Chinese Express Korean Noodles (Japchae) with Vegetables are being recalled due to undeclared egg allergen. The 54 containers distributed in Missouri may pose a health risk to consumers with egg allergies.

    Product
    LuLu Chinese Express Korean Noodles (Japchae) w/ Vegetables. Net Wt 16oz.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0029-2024·2023-10-18

    Hemodialysis machines recalled for potential printed circuit board contamination

    Fresenius Medical Care is recalling 733 2008T Hemodialysis Systems without CDX due to potential PCBA leaching from tubing. This FDA Class I recall affects units distributed nationwide.

    Product
    2008T Hemodialysis System without CDX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0042-2024·2023-10-18

    FDA recalls BREXAFEMME tablets due to cross-contamination with ezetimibe

    The FDA is recalling BREXAFEMME antifungal tablets due to potential cross-contamination with ezetimibe during manufacturing, with two lot numbers distributed nationwide.

    Product
    BREXAFEMME (Ibrexafungerp) tablets 150 mg, 4 count cartons, Rx Only, Manufactured for and distributed by SCYNEXIS, Inc., Jersey City, NJ 07302 NDC 75788-115-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0030-2024·2023-10-18

    2008T Hemodialysis System recalled for potential PCBA leaching from tubing

    Fresenius Medical Care is recalling 733 units of the 2008T Hemodialysis System due to potential leaching of printed circuit board material from machine tubing. Patients using affected devices should contact their healthcare provider.

    Product
    2008T Hemodialysis System w/Bibag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0007-2024·2023-10-18

    Syringes with Luer Lock Recalled for Blood Backfill and Foreign Material Risk

    Fresenius Medical Care is recalling 3ML syringes with Luer Lock due to potential blood backfill leakage and foreign material contamination. The recall affects 124,773 boxes distributed nationwide.

    Product
    3ML Syringe Luer Lock with needle 20GX1, Part Number 15-03ML-0, 100 per box, 24 boxes per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0033-2024·2023-10-18

    Hemodialysis machines recalled for potential PCBA leaching from tubing

    Fresenius Medical Care is recalling 733 units of 2008T HD hemodialysis machines nationwide due to potential PCBA leaching from tubing. The FDA classified this as a Class I recall.

    Product
    2008T HD SYS. CDX W/BIBAG BLUESTAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0006-2024·2023-10-18

    10ML Syringe Luer Lock Recalled for Potential Blood Backfill Leakage

    Fresenius Medical Care is recalling 124,773 boxes of 10ML Syringe Luer Lock syringes due to potential blood backfill leakage and foreign material contamination.

    Product
    10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0031-2024·2023-10-18

    Medical device manufacturer recalls hemodialysis machines for potential PCBA leaching

    Fresenius Medical Care is recalling 733 units of the 2008T GEN 2 Bibag hemodialysis machine due to potential printed circuit board assembly material leaching from tubing. All affected units were distributed domestically.

    Product
    2008T GEN 2 Bibag without CDX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0032-2024·2023-10-18

    Hemodialysis Machines Recalled Due to Potential PCBA Leaching

    Fresenius Medical Care is recalling 733 hemodialysis machines nationwide due to potential printed circuit board material leaking from tubing.

    Product
    2008T HD SYS. CDX BLUESTAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V698000·2023-10-17

    Ferrari Recalls SF90 Models Due to Turbocharger Oil Leak Fire Risk

    Ferrari is recalling 2022-2024 SF90 Stradale and Spider vehicles because a defective turbocharger oil pipe may leak, increasing fire risk.

    Product
    FERRARI — FERRARI SF90 SPIDER, SF90 STRADALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V697000·2023-10-17

    Proterra Transit Buses Recalled for Inverter Power Loss Risk

    Proterra is recalling 2019-2022 ZX5 and Catalyst 800V transit buses due to inverter transistor overheating risk. A transistor failure can cause loss of power steering and drive power, increasing crash risk.

    Product
    PROTERRA — PROTERRA ZX5, CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·049-2023·2023-10-16

    Phu Huong Recalls Beef and Poultry Meatballs Due to Listeria

    Phu Huong Food Company is recalling approximately 602 pounds of ready-to-eat beef and chicken meatballs due to possible Listeria monocytogenes contamination.

    Product
    Phu Huong Food Company, Inc. — Phu Huong Food Company Recalls Ready-To-Eat Beef and Poultry Meatball Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·048-2023·2023-10-16

    Mrs. Pasta Recalls Frozen Meat Pasta Produced Without Federal Inspection

    Mrs. Pasta is recalling approximately 4,544 pounds of frozen meat pasta products because they were produced without the benefit of federal inspection.

    Product
    Mrs. Pasta Recalls Frozen Meat Pasta Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·047-2023·2023-10-13

    Don Miguel Recalls Frozen Carne Asada Burritos Due to Listeria Risk

    Don Miguel Foods is recalling approximately 10,642 pounds of frozen ready-to-eat carne asada burritos due to possible Listeria monocytogenes contamination.

    Product
    Don Miguel Mexican Foods, Inc. — Don Miguel Foods Recalls Frozen Ready-To-Eat Carne Asada Burrito Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V693000·2023-10-13

    Arcimoto Recalls 2023 FUV and MUV Motorcycles for Steering Defect

    Arcimoto is recalling 2023 FUV and MUV hybrid electric motorcycles because insufficient thread engagement in the tie rods could cause separation and loss of steering control.

    Product
    ARCIMOTO — ARCIMOTO FUV, MUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V687000·2023-10-13

    Ford Recalls 2021-2022 Mustang Mach-E Vehicles for Battery Contactor Overheating

    Ford is recalling 2021-2022 Mustang Mach-E vehicles with extended range batteries because high voltage battery contactors may overheat, potentially causing a loss of drive power and increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V683000·2023-10-12

    GM Recalls 2023-2024 BrightDrop Zevo 600 for Air Bag Deployment Issue

    General Motors is recalling 2023-2024 BrightDrop Zevo 600 vehicles with optional passenger jump seats due to a trim panel that may interfere with the right-side roof-rail air bag.

    Product
    BRIGHTDROP — BRIGHTDROP ZEVO 600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V685000·2023-10-12

    Hyundai Translead Recalls 2022-2024 Extended Chassis Due to Weld Defects

    Hyundai Translead is recalling 2022-2024 extended chassis because improperly welded cross braces may detach, posing a road hazard or causing brake lock.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD 20'/40' 12PIN EXTEN CHASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0037-2024·2023-10-11

    FDA Recalls Dr. Berne's MSM Drops Due to Non-Sterility Concerns

    Dr. Berne's MSM DROPS 5% Solution was recalled by the FDA for non-sterility issues. Lot 6786, with expiration date March 31, 2025, is distributed nationwide and internationally.

    Product
    Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, [email protected], UPC 00854582001111.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0003-2024·2023-10-11

    Arrow Central Venous Catheter Recalled for Incorrect Lidstock Labeling

    Arrow International is recalling 380 units of its Arrowg+ard Blue Plus Four-Lumen central venous catheter (model CDC-45854-P1A, lot 13F22L0806) due to incorrect product code and name listed on the package lidstock.

    Product
    Arrow Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0002-2024·2023-10-11

    Arrow ErgoPack central venous catheter recalled for incorrect labeling

    ARROW INTERNATIONAL is recalling 180 units of the Arrow ErgoPack Complete CVC catheter (Lot 33F23B0723) distributed in the US because the product code and product name were incorrectly listed on the kit's label.

    Product
    Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0001-2024·2023-10-11

    Arrow PICC Catheters Recalled for Incorrect Product Label Information

    Arrow International recalled 1,173 PICC line units due to incorrect product code and name on packaging labels. Affected lot 33F23B0781 was distributed in the US.

    Product
    Arrow ErgoPack, Pressure Injectable Arrowg+ard Blue Advance Two-Lumen PICC pre-loaded with Arrow VPS Precision Stylet, REF CDC-45552-VPS2; Catheter: Percutaneous Implanted Long-Term Intravascular Catheter Stylet: Diagnostic Intravascular Catheter
    Category
    Medical Device
    Distribution
    0 states