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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25551–25575 of 90145

  • SevereNHTSA·22V356000·2022-05-19

    Reiser Recalls 2022 Trailers Due to Improperly Welded Couplers

    Reiser is recalling 2022 WCH, LSA, LTA, L, SBS, and LATV trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.

    Product
    REISER — REISER LTA, LSA, L, LATV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V354000·2022-05-19

    Hyundai Elantra and Accent seat belt pretensioners may explode in crash

    Hyundai is recalling certain 2020-2022 Accent and 2021-2022 Elantra models due to seat belt pretensioners that may explode during a crash, potentially projecting metal fragments and injuring occupants. Dealers will secure them with a cap at no charge.

    Product
    HYUNDAI — HYUNDAI ELANTRA HYBRID, ELANTRA, ACCENT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V357000·2022-05-19

    Bigfoot Recalls 2022 Travel Trailers Due to Gas Leak Risk

    Bigfoot is recalling 2022 25B17FB travel trailers because damaged burner control valves may cause a gas leak, increasing the risk of fire.

    Product
    BIGFOOT — BIGFOOT 25B17FB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V359000·2022-05-19

    2022 Chevrolet Blazer driver's seat frame weld defect

    General Motors is recalling certain 2022 Chevrolet Blazer vehicles due to an improper weld in the driver's seat cushion frame that may fail to adequately restrain the driver in a crash.

    Product
    CHEVROLET — CHEVROLET, CADILLAC MALIBU, EQUINOX, XT4, BLAZER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V358000·2022-05-19

    Coach House motorhomes recalled for cooktop gas leak fire risk

    Coach House is recalling certain 2021-2022 Platinum, Platinum II, and Arriva motorhomes with cooktop burner control valves that may leak gas and increase fire risk. Dealers will replace the cooktop at no cost.

    Product
    COACH HOUSE — COACH HOUSE ARRIVA, PLATINUM II, PLATINUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1058-2022·2022-05-18

    Valencian Almonds Recalled Due to Undeclared Peanut Contamination

    Culinary Collective is recalling Valencian Almonds due to potential peanut contamination not declared on the label. The affected products were distributed in Colorado, Montana, New York, and Oregon.

    Product
    Valencian Almonds FS Skinless, MZ502, packaged in bulk package 5 KG. Net Wt. 352 oz./22 lb. (2 bags @ 11 lb.). UPC 5 901234 123457. Ingredients: Valencian Almonds, sunflower oil, sea salt and antioxidants (mixed tocopherols and rosemary extract to preserve freshness).…
    Category
    Food
    Distribution
    4 states
  • SevereUSDA FSIS·016-2022·2022-05-18

    USDA Recalls Ready-to-Eat Pork Sausage Due to Metal Contamination

    America New York Ri Wang Food Group is recalling ready-to-eat pork sausage products nationwide due to possible metal contamination.

    Product
    America New York Ri Wang Food Group Co., Ltd. — America New York Ri Wang Food Group Co., Ltd Recalls Ready to Eat Pork Sausage Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V350000·2022-05-18

    Oliver Travel Trailers Recall Elite Models Due to Gas Leak Risk

    Oliver Travel Trailers is recalling 2021-2022 Legacy Elite models because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    OLIVER TRAVEL TRAILERS — OLIVER TRAVEL TRAILERS LEGACY ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0856-2022·2022-05-18

    SyrSpend SF Suspending Base Recalled for Burkholderia Contamination

    Fagron is recalling SyrSpend SF Suspending Base, Cherry Flavored (NDC 51552-1123-5 and 51552-1123-9) due to contamination with Burkholderia gladioli. This FDA Class I recall affects medication used in compounding.

    Product
    SyrSpend SF Suspending Base, Cherry Flavored, packaged in a) 500mL bottles (NDC 51552-1123-5) and b) 4L bottles (NDC 51552-1123-9), Rx Only, Manufactured for Fagron, Inc., St. Paul, MN 55120.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1009-2022·2022-05-18

    FDA Recalls Accula SARS-CoV-2 Test for False Positive Risk

    Mesa Biotech is recalling approximately 6,162 units of the Accula SARS-CoV-2 Test due to an increased risk of false positive results, which could delay correct diagnosis and treatment.

    Product
    Accula SARS-CoV-2 Test, REF: COV4100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1045-2022·2022-05-18

    COVID-19 Antigen Test Kit Distributed Without FDA Authorization or Clearance

    The FDA is recalling 17,000 units of Joysbio SARS-CoV-2 Antigen Rapid Test Kits distributed in Alabama and Georgia. The tests were sold without FDA clearance or authorization for marketing in the United States.

    Product
    Joysbio SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold); COVID 19 Test
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-1044-2022·2022-05-18

    COVID-19 Rapid Antigen Test Kits Recalled for Unauthorized Distribution

    Woodside Acquisitions Inc. recalled 34,240 Oral Rapid SARS-CoV-2 Antigen Test Kits distributed in Alabama and Georgia. The tests were distributed without FDA clearance or authorization for marketing.

    Product
    Oral Rapid SARS-CoV-2 Antigen Rapid Test Kit; COVID 19 Test
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Food)·F-1057-2022·2022-05-18

    Ramen Hero vegan shoyu ramen recalled for undeclared egg allergen

    Ramen Hero is recalling certain lots of its Vegan Shoyu Ramen meal kits because they contain egg noodles despite egg not being listed on the label, posing a risk to people with egg allergies.

    Product
    Ramen Hero - Vegan Shoyu ramen (Hippie Van) Ramen noodles in a soy sauce infused vegan broth with a vegan meat ragu, roasted tomato, bell pepper and zucchini blend, and seaweed. Kits are in a frosted meal kit stand up pouch. Net Wt. 20.05 oz. (1.25 lb.) 568 g UPC: 60003…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1057-2022·2022-05-18

    Chemotherapy Infusion Bag Adaptor May Disconnect and Spill Hazardous Drugs

    Simplivia Healthcare is recalling OnGuard2 CSTD Bag Adaptors because they may disconnect from infusion bags, potentially spilling hazardous medications.

    Product
    OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product, Product code MG412143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1043-2022·2022-05-18

    Medtronic IN.PACT AV Balloon Catheter: Damaged Packaging May Affect Sterility

    Medtronic is recalling IN.PACT AV paclitaxel-coated balloon catheters because packaging damage may result in loss of sterility. The devices were distributed worldwide and in the United States.

    Product
    Medtronic IN.PACT AV, Paclitaxel-coated PTA Balloon Catheter, REF: IAV06008008P, Sterile EO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1059-2022·2022-05-18

    VITEK 2 Systems Software Issue May Produce Incorrect Antibiotic Test Results

    bioMerieux VITEK 2 bacterial identification systems have a software defect where antibiotic susceptibility and synergy test results transmitted to laboratory systems may omit user or automated corrections, potentially leading to incorrect test interpretation.

    Product
    VITEK 2 Systems and VITEK 2 with MYLA.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·22V352000·2022-05-18

    Can-Am Recalls 2015-2019 Spyder RT and F3 for Sprocket Defect

    Bombardier is recalling 2015-2019 Can-Am Spyder RT and F3 motorcycles because a defective front sprocket may wear prematurely, causing a loss of drive power and increasing crash risk.

    Product
    CAN-AM — CAN-AM SPYDER RT, SPYDER F3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1050-2022·2022-05-18

    O-Organic Sea Salt Popcorn Recalled for Potential Milk Allergen Contamination

    Snak King Corporation recalls O-Organic Sea Salt Popcorn due to milk allergen found in the production line's recycle chute. Consumers with milk allergies should not consume this product.

    Product
    12/5 oz. bags of O-Organic Sea Salt Popcorn. UPC Code: 79893403038
    Category
    Food
    Distribution
    18 states
  • HighFDA (Devices)·Z-1055-2022·2022-05-18

    Flexible Bronchoscope Recalled Due to Inadequate Disinfection Process

    Karl Storz is recalling flexible bronchoscopes due to potential failure of the disinfection process. The devices may not eliminate microorganisms adequately, posing an infection risk to patients.

    Product
    11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1053-2022·2022-05-18

    Ethicon STRATAFIX Surgical Sutures Recalled for Incorrect Needle Type and Size

    Ethicon is recalling STRATAFIX surgical sutures (lots AAHM529 and AAHQ049) due to component mix-ups resulting in incorrect needle types, sizes, or suture lengths. 2,808 units distributed internationally are affected.

    Product
    STRATAFIX SPIRAL PGA-PCL UNI UD sizes: [20CM USP2-0(M3) S/A RB-1, product code: SXMD1B403-12] and [30CM USP2-0(M3) S/A PS-1, product code: SXMD1B100-12].
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·22V351000·2022-05-18

    2022 Lucid Air Display Wiring Harness May Disable Critical Safety Screens

    Lucid is recalling 2022 Air vehicles because the display wiring harness may not be secured properly, potentially disabling screens that show speedometer, gear selection, and warning lights.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0855-2022·2022-05-18

    MVASI Cancer Drug Recalled for Loose Container Crimp

    Amgen is recalling specific lots of MVASI (bevacizumab-awwb) injection due to a loose crimp defect in the container that could compromise container integrity. Patients should contact their healthcare provider.

    Product
    MVASI (bevacizumab-awwb), Injection, For Intravenous Infusion After Dilution, 100 mg/4 ml, Single dose vial, Rx only, Manufactured by Amgen Inc. Thousand Oaks, CA 91320-1799, NDC 55513-0206-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1074-2022·2022-05-18

    Phototherapy Units Recalled for Software Bug Causing Incorrect Dosing

    Daavlin's 4 Series CX phototherapy units are recalled due to a software defect that can cause incorrect dosing (over or under) when resuming interrupted treatments.

    Product
    4 Series CX phototherapy units equipped with Daavlin's ClearLink Control System software versions v3.03h and 3.04v. M4 Ser CX 311-20 120-240V 50/60Hz, item # 807QS0020CX6.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1055-2022·2022-05-18

    Bwell Bird's Nest Lychee Beverage recalled for deficient packaging and spoilage risk

    Eastland Food Corporation is recalling Bwell Bird's Nest Beverage in Lychee Flavor due to deficient packaging material that could lead to premature spoilage. Approximately 1,699 cases were distributed to retail stores across 33 states.

    Product
    Bwell Bird's Nest Beverage Lychee Flavor NET 8.45 FL OZ (250mL) UPC 8373726350 24 bottles per case
    Category
    Food
    Distribution
    34 states
  • HighFDA (Devices)·Z-1041-2022·2022-05-18

    Philips Hemodynamic Application fails to set neonatal blood pressure mode

    The Philips Hemodynamic Application, Model 722463, may not automatically switch to neonatal mode for blood pressure monitoring, potentially applying excessive cuff pressure that could cause bruising, nerve damage, or bone deformity in newborns.

    Product
    Philips Hemodynamic Application, Model Number 722463, Software Version Number: R1.2.2 and R1.2.3. For visualization and analysis of patient hemodynamic data in the Philips Interventional Hemodynamic System.
    Category
    Medical Device
    Distribution
    6 states