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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10076–10100 of 27638

  • HighFDA (Devices)·Z-0309-2025·2024-11-13

    DeRoyal Surgical Procedure Pack Smoke Evacuation Pencil Recalled

    DeRoyal is recalling surgical procedure pack products containing a Stryker SafeAir Smoke Evacuation Pencil that may activate without manual input or remain active after buttons are released. The malfunction poses a risk of injury during surgical procedures.

    Product
    DeRoyal CHILDREN'S LAPTRACEPACK, 89-9362.06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0325-2025·2024-11-13

    Cardiac stress testing system may assign duplicate exam identifiers to patients

    Hillrom Welch Allyn XScribe cardiac stress testing systems may assign duplicate exam identifiers, potentially causing patient data mismatches in medical record systems.

    Product
    Hillrom Welch Allyn XScribe Cardiac Stress Testing System; Programmable Diagnostic Computer
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Drugs)·D-0036-2025·2024-11-13

    Morphine Sulfate Extended-Release Tablets Recalled for Impurities and Degradation

    Dr. Reddy's Laboratories is recalling Morphine Sulfate Extended-Release Tablets 15 mg nationwide due to failed impurity and degradation specifications. Patients taking affected lots should contact their healthcare provider immediately.

    Product
    Morphine Sulfate Extended-Release Tablets 15 mg, 100-count per bottle, Rx Only, Manufactured by Mayne Pharma, Greenville, NC 27834, NDC 51862-185-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0107-2025·2024-11-13

    MyChai Chai Tea Concentrate recalled for improper pH and missing production records

    My Chai Inc is recalling MyChai Chai Tea Concentrate KALI nationwide because pH levels were found above 4.1 and production records are missing. Consumers should not consume the product.

    Product
    MyChai Chai Tea Concentrate KALI, 68 fl. oz. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that is induction sealed during the bottling process. Shelf stable 3 year expiration from date of manufacture Ingredients: Water, Sugar, Organic Black Tea Ex
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0307-2025·2024-11-13

    DeRoyal Children's Surgical Pack Recalled for Smoke Pencil Malfunction

    DeRoyal is recalling certain lots of children's surgical procedure packs due to reports that the included Stryker smoke evacuation pencil may activate without manual input or remain active after buttons are released.

    Product
    DeRoyal CHILDREN'S GENERAL TRACEPACK, REF 89-9342-06
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0285-2025·2024-11-13

    Endoscopic Vessel Harvesting System Recalled for Assembly Defect

    Zimmer recalls the Venapax XL endoscopic vessel harvesting system due to assembly defects that may cause endoscope interference during surgery. A Gen 5 tail piece was incorrectly assembled to Gen 4 devices, affecting 432 units nationwide.

    Product
    Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally invasive surgery allowing access for vessel harvesting and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass. Item Number: VPX4000 (7273)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V761000·2024-11-10

    Hyundai Nexo Hydrogen Pressure Relief Device Defect Creates Fire Risk

    Hyundai is recalling 2019-2024 Nexo vehicles because the hydrogen pressure relief device may fail and leak, creating a fire risk. Owners are advised to park outside until the repair is complete.

    Product
    HYUNDAI — 2020 HYUNDAI NEXO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V669000·2024-11-09

    Tiffin Allegro Bay motorhome subframe truss collapse fire risk recall

    Tiffin is recalling 2022–2025 Allegro Bay motorhomes due to subframe truss collapse that can pinch electrical wiring and cause electrical arcing, increasing fire risk.

    Product
    TIFFIN — 2022 TIFFIN ALLEGRO BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V593000·2024-11-08

    Volkswagen Recalls 2024 Atlas Cross Sport for Engine Bearing Defect

    Volkswagen is recalling 2024 Atlas and Atlas Cross Sport vehicles because engine bearings may fail, causing engine stalls and increasing the risk of crashes and fires.

    Product
    VOLKSWAGEN — 2024 VOLKSWAGEN ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25038·2024-11-07

    Portable Lamps Recalled Due to Fire Hazard from Battery Overheating

    About 5,300 Tala Muse Portable Lamps are recalled due to fire hazard from battery overheating. One incident caused property damage; consumers should stop using the lamps and contact Tala for a free replacement bulb.

    Product
    Tala Muse Portable Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25036·2024-11-07

    Smart Electric Space Heaters Recalled for Fire and Burn Hazards

    GoveeLife and Govee smart electric space heaters can overheat and pose fire and burn hazards due to non-compliance with UL 1278 safety standards. About 512,500 units are affected.

    Product
    GoveeLife and Govee Smart Electric Space Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25033·2024-11-07

    Baofali 4-in-1 Microfiber Crib Bumpers Recalled for Suffocation Hazard

    Baofali 4-in-1 Microfiber Crib Safety Bumpers sold on Temu.com violate the federal crib bumper ban and pose a suffocation hazard to infants. About 390 units were sold from June through August 2024.

    Product
    Baofali 4-in-1 Microfiber Crib Safety Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25030·2024-11-07

    Dreamgro Lullaby Travel Soothers Recalled Due to Choking Hazard

    Dreamgro Lullaby mermaid travel soothers are recalled because a gold-colored soft star can detach, posing a choking hazard to infants. No injuries have been reported, but one detachment incident was confirmed.

    Product
    Dreamgro Lullaby mermaid travel soothers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25031·2024-11-07

    Kyte Baby Slumber Suits Recalled Due to Flammability Violation, Burn Injury Risk

    Kyte Baby is recalling about 20,500 Slumber Suits sold from November 2022 to March 2024 because they violate federal flammability regulations for children's sleepwear, posing a risk of burn injuries. No injuries have been reported.

    Product
    Kyte Baby Slumber Suits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25032·2024-11-07

    Guava Roam strollers recalled due to brake failure and fall hazards

    Guava Roam strollers are recalled because the brakes can fail to engage or unexpectedly disengage, posing fall and injury hazards to children. No injuries have been reported.

    Product
    Guava Roam Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25034·2024-11-07

    Wolf Dual Fuel ranges with infrared griddles recalled for fire and burn hazards

    Wolf Appliance is recalling about 44,000 Dual Fuel ranges with infrared griddles due to a short-circuit hazard. Liquid spillage can unexpectedly activate the griddle, posing burn and fire risks. No injuries have been reported.

    Product
    Wolf Dual Fuel ranges with infrared griddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0077-2025·2024-11-06

    Los Andes Foods Sweet Corn Pancakes Recalled for Undeclared Wheat Allergen

    Los Andes Foods Sweet Corn Pancakes are being recalled because they contain undeclared wheat allergen. Consumers with wheat allergies should not consume the product and should discard it.

    Product
    Los Andes Foods Sweet Corn Pancakes, Cachapas de Maiz, NET WT. 24 Oz., 5 units, KEEP REFRIGERATED
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0141-2025·2024-11-06

    GE Healthcare Infant Incubator Recall: Airborne Formaldehyde Off-Gassing

    GE Healthcare Giraffe Incubator Carestation CS1 units may release airborne formaldehyde residue during initial use. Manufacturer notified customers in June 2023 to run incubators for one week to off-gas any residual formaldehyde, which can cause eye irritation.

    Product
    GE Healthcare Giraffe Incubator Carestation CS1, Infant Incubator. Model Numbers: 1) 2082844-002-01040417; 2) 2082844-002-01044956; 3) 2082844-002-01058424; 4) 2082844-002-01069017; 5) 2082844-002-01089666; 6) 2082844-002-01090474; 7) 2082844-002-01091269; 8) 208
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-0208-2025·2024-11-06

    Phasitron5 breathing circuits recalled for nickel-coated spring discoloration

    Percussionaire Corporation is recalling Phasitron5 breathing circuits (P5-10, P5-HC, P5-UC-10) due to discolored fluid caused by an unintended nickel coating on the spring component reacting with medicated mist. 43,830 devices have been distributed across the U.S.

    Product
    Phasitron5 Breathing Circuit (P5-10, P5-HC, P5-UC-10). component of Intrapulmonary Percussive Ventilation, used to provide airway clearance therapy
    Category
    Medical Device
    Distribution
    40 states
  • SevereFDA (Food)·F-0073-2025·2024-11-06

    Jack & the Green Sprouts Alfalfa Recalled for Possible Listeria Contamination

    Jack & the Green Sprouts Alfalfa sprouts (5 oz containers) are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Iowa, Minnesota, and Wisconsin.

    Product
    Jack & the Green Sprouts Alfalfa, Net Weight 5 oz (142g). UPC 7 63247-19891 5 Keep Refrigerated. Product of USA. Jackandthegreensprouts.com, River Falls, WI 54022. EXPANDED 10/4/2024: Product was packaged in 5 oz containers that were packed in 6 count or 12 count shippi
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0129-2025·2024-11-06

    Dakota Tom's The Gambler Sandwiches Recalled for Potential Listeria Contamination

    Dakota Tom's The Gambler sandwiches are recalled for potential Listeria monocytogenes contamination. Products were distributed to retail locations in ND, SD, WY, IA, and MN, with expiration dates September 1–November 28, 2024.

    Product
    The Gambler, Dakota Toms brand, Net Wt 7.8 oz, individual pre-packaged components in MEP packaging, UPC 737296601788
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·F-0120-2025·2024-11-06

    Shirakiku Korean Seaweed Recalled for Undeclared Sesame Allergen

    Wismettac Asian Foods recalls Shirakiku Korean Seasoned Seaweed due to incorrect product labeling that fails to disclose sesame. Affected products were distributed in CA, AZ, TX, NM, WA, NY, and NV.

    Product
    The outer package of the recalled product, Shirakiku Korean Seasoned Seaweed Korean Seaweed, is INCORRECTLY labeled as follows: (Principal Display Panel) Roasted Seaweed 10-0.91 OZ (26 G) PACKAGES (NET WT 9.1 OZ (260 G). (Back Display) ROASTED SEAWEED Organic Yaki Nori Ingredient
    Category
    Food
    Distribution
    7 states