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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26826–26850 of 90158

  • HighFDA (Devices)·Z-0594-2022·2022-02-16

    GE Healthcare MRI Systems Recalled for Inadequate Cryogen Ventilation

    GE Healthcare is recalling MRI superconducting magnets with cryogen ventilation system defects not meeting safety requirements. The recall affects 17,228 devices distributed across the US and internationally.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750 3.0T System, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0632-2022·2022-02-16

    Natural Way Cheese Chive Cheese Curds Recalled for Improper Milk Storage

    Natural Way Cheese Chive Cheese Curds (12oz bags) distributed in Michigan and Indiana are recalled because milk used was stored beyond the required 72-hour tank cleaning interval, creating a risk of bacterial growth.

    Product
    Natural Way Cheese Chive Cheese Curds, retail 12oz plastic bag UPC 8 10056 75107 4, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0605-2022·2022-02-16

    GE Healthcare MR system magnets recalled due to cryogen ventilation defect

    GE Healthcare is recalling 17,228 MR superconducting magnet components due to a cryogen ventilation system that may not meet required venting specifications.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Infinity MR System, SIGNA Infinity MR System with Excite Technology, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0586-2022·2022-02-16

    Diagnostic Control Microorganism Recalled for Incorrect Test Results

    Diagnostic control microorganisms manufactured by Microbiologics Inc are recalled for returning incorrect antibiotic susceptibility test results. These controls failed quality specifications and could cause inaccurate lab test results.

    Product
    LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic Control microorganisms
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0565-2022·2022-02-16

    MIC Percutaneous Endoscopic Gastrostomy Kits Recalled for Oversized Retention Bolster

    Avanos Medical is recalling the MIC Percutaneous Endoscopic Gastrostomy (PEG) Kit because the external retention bolster may be oversized relative to the tube. Approximately 2,652 units have been distributed in the US, Canada, and Chile.

    Product
    MIC* Percutaneous Endoscopic Gastrostomy PEG Kit - 20 Fr-PULL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0593-2022·2022-02-16

    GE Healthcare MRI Systems Cryogen Ventilation System Defect Recall

    GE Healthcare is recalling Discovery MR750w 3.0T MRI systems due to cryogen ventilation systems that may not meet FDA venting requirements. Approximately 17,228 devices were affected.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750w 3.0T System, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0639-2022·2022-02-16

    Cheese Curds Recalled for Improper Milk Tank Sanitation

    Natural Way Cheese hickory smoke flavor cheese curds are recalled because milk used in the product was stored in a holding tank beyond the required 72-hour cleaning interval. The recall affects products distributed in Michigan and Indiana.

    Product
    Natural Way Cheese Hickory Smoke Flavor Cheese Curds, retail 12oz plastic bag UPC 8 10056 75017 6, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0579-2022·2022-02-16

    Baxter CAPD Transfer Sets may crack or leak when exposed to cleaning chemicals

    Baxter CAPD MiniCap Transfer Set II units may leak or crack when cleaned with chemicals including bleach, hydrogen peroxide, or solvents. The recall affects 8,928 units distributed worldwide.

    Product
    Baxter CAPD System Transfer Set (CAPD MiniCap Transfer Set II (24cm)), Code No. T5C4482
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0580-2022·2022-02-16

    Baxter CAPD Transfer Sets May Leak if Cleaned with Certain Chemicals

    Baxter Healthcare is recalling CAPD MiniCap Transfer Set II units worldwide because certain cleaning products containing chemicals like hydrogen peroxide, bleach, and solvents may cause the sets to leak or crack.

    Product
    Baxter CAPD System Transfer Set (CAPD MiniCap Transfer Set II (34cm)), Code No. T5C4484
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0799-2022·2022-02-16

    Simply Goodfats MCT Oil Powder Recalled for Undeclared Milk Allergen

    Simply Goodfats Creamy MCT Unflavored MCT Oil Powder is recalled due to undeclared milk allergen. The product was distributed to online customers in the US.

    Product
    Simply Goodfats Creamy MCT Unflavored MCT Oil Powder 10.5 OZ. Packaged White HDPE Plastic. UPC Code: 857826008594 Expiration dates: 11/30/2021 2/28/2022 7/31/2021
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0730-2022·2022-02-16

    Amy's Vegan Rice Mac & Cheese Recall: Undeclared Milk Allergen

    Amy's Kitchen is recalling its Vegan Organic Rice Mac & Cheese due to undeclared milk detected during testing. The product is labeled dairy-free, posing a risk to consumers with milk allergies.

    Product
    Amy's Vegan Organic Rice Mac & Cheese; frozen; 8 oz. (227 g) individually packaged serving; in trays with plastic overwrap, inside preprinted cardboard boxes; UPC 04227200432; Amy's Kitchen, Inc., P.O.Box 7129, Petaluma, CA 94955 8 or 12 retail units per case; Organic Gluten…
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-0575-2022·2022-02-16

    Baxter MiniCap PD Transfer Set Recall—Damage from Cleaning Products

    Baxter Healthcare is recalling MiniCap Extended Life PD Transfer Sets worldwide because cleaning products containing hydrogen peroxide, bleach, alcohol, or solvents may cause the devices to leak or crack.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, REF R5C4482
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0739-2022·2022-02-16

    Lily's Peppermint Flavor Baking Chips Recalled for Undeclared Soy Allergen

    Lily's Sweets is recalling 7 oz. pouches of Peppermint Flavor Baking Chips because they contain undeclared soy lecithin, a common allergen. The product was distributed to 22 U.S. states.

    Product
    Lily s Peppermint Flavor Baking Chips, 7 oz. Pouch
    Category
    Food
    Distribution
    22 states
  • HighFDA (Devices)·Z-0634-2022·2022-02-16

    Universal Chuck Surgical Instrument Handle May Detach and Release Ball Bearings

    The Universal Chuck instrument handle may loosen and release ball bearings onto the surgical field. If not recovered, these bearings could delay surgery and potentially cause infection or tissue damage.

    Product
    Universal Chuck-The Universal Chuck is an Instrument Handle provided as an alternative instrument available for use in the TN-ADVANCED" Tibial Nailing System (TNA), TFN-ADVANCED" Proximal Femoral Nailing System (TFNA), RFN-ADVANCED" Retrograde Femoral Nailing System (RFNA)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0635-2022·2022-02-16

    Natural Way Cheese Ranch Cheese Curds Recalled for Improper Milk Storage

    Natural Way Cheese is recalling Ranch Cheese Curds due to milk stored in a holding tank beyond the required 72-hour cleaning interval. The recalled products were distributed in Michigan and Indiana.

    Product
    Natural Way Cheese Ranch Cheese Curds, retail 12oz plastic bag UPC 8 10056 75014 5, 12 retail units per wholesale case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0733-2022·2022-02-16

    Fresh cheese recalled for potential coliform contamination

    Quesos La Ricura Mi Ranchito Fresh Cheese with Hot Peppers may contain elevated levels of coliform bacteria. Approximately 2,478 units were distributed across 11 states with a sell-by date of March 20, 2022.

    Product
    Quesos La Ricura Mi Ranchito Fresh Cheese with Hot Peppers, 14. 0z.
    Category
    Food
    Distribution
    10 states
  • HighCPSC·22083·2022-02-16

    Valco Baby Snap Duo Trend Strollers recalled for front wheel breakage hazard

    Valco Baby is recalling Snap Duo Trend strollers because the front wheels can break off during use, causing the stroller to fall unexpectedly. Consumers should stop using the stroller immediately and contact Valco Baby for a free replacement wheel assembly.

    Product
    Valco Baby Snap Duo Trend Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0632-2022·2022-02-16

    Orthopedic knee replacement component recalled for adhesive residue contamination

    DePuy Orthopaedics is recalling 3 units of ATTUNE REVISION DISTAL FEMORAL AUGMENT due to adhesive residue that could cause tissue irritation or infection if not detected before surgery.

    Product
    ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0601-2022·2022-02-16

    GE Healthcare MRI Cryogen Ventilation System Defect Recall

    GE Healthcare is recalling 17,228 MRI systems due to a potential defect in the cryogen ventilation system that may not meet venting requirements. This Class II recall affects systems distributed nationwide and internationally.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare Optima MR450w 1.5T, Optima MR450w GEM system, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V567000·2022-02-16

    2017-2021 Freightliner Cascadia Brake Lights May Remain Illuminated

    Daimler Trucks North America is recalling 2017-2021 Freightliner Cascadia trucks because brake lights may remain illuminated after braking. This increases crash risk by making drivers unaware of actual braking.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0618-2022·2022-02-16

    GE Healthcare MRI Systems Cryogenic Ventilation System Failure Recall

    GE Healthcare is recalling 17,228 MR Vectra MRI systems because the cryogenic ventilation system may not meet required venting specifications.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare MR Vectra System, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0573-2022·2022-02-16

    Baxter PD Transfer Sets may leak or crack from common cleaning products

    Certain cleaning products can damage Baxter MiniCap Extended Life PD Transfer Sets, causing them to leak or crack. Baxter is recalling approximately 61,290 units sold worldwide.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp, 5C4482EJ
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0609-2022·2022-02-16

    GE Healthcare 1.5T SIGNA MRI systems recalled for ventilation defect

    GE Healthcare is recalling 17,228 of its 1.5T SIGNA HDe MR imaging systems because the cryogenic ventilation system does not meet required venting standards.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare 1.5T SIGNA HDe MR System, nuclear magnetic resonance imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0578-2022·2022-02-16

    Baxter MiniCap PD Transfer Sets may leak or crack with certain cleaners

    Certain cleaning products can damage Baxter MiniCap PD Transfer Sets, potentially causing them to leak or crack. This could affect the safety of peritoneal dialysis treatment if the damaged set is used.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Long, REF R5C4484
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0587-2022·2022-02-16

    QC Control Materials KWIK-STIK AST-GP Produce Incorrect Test Results

    Microbiologics Inc recalls KWIK-STIK AST-GP quality control materials that produce incorrect antibiotic susceptibility test results. Two lot numbers were distributed worldwide.

    Product
    QC Sets and Panels, KWIK-STIK AST-GP (4 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms
    Category
    Medical Device
    Distribution
    Distributed nationwide