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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22776–22800 of 26059

  • HighFDA (Food)·F-0642-2022·2022-02-16

    Natural Way Cheese Cheddar Curds recalled for improper milk storage

    Natural Way Cheese is recalling Cheddar Cheese Curds because milk used in production was stored in a holding tank for longer than the required 72-hour cleaning interval, creating potential for contamination.

    Product
    Natural Way Cheese Cheddar Cheese Curds, retail 12oz plastic bag UPC 8 10056 75023 7, 12 retail units per wholesale case, and sold in 10lbs wholesale plastic bag as well
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0604-2022·2022-02-16

    GE Healthcare MR Superconducting Magnets Recalled for Ventilation Defect

    GE Healthcare recalled 17,228 superconducting magnets, a component of SIGNA 1.5T MR systems, due to a cryogen ventilation system that may not meet venting requirements. Systems are distributed nationwide and internationally.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA 1.5T TwinSpeed MR System, nuclear magnetic resonance system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0570-2022·2022-02-16

    Baxter peritoneal dialysis transfer sets may crack or leak with certain cleaners

    Baxter MiniCap Extended Life PD Transfer Sets may be damaged by certain cleaning products containing hydrogen peroxide, bleach, alcohol, or solvents, potentially causing leaking or cracking. No injuries have been reported.

    Product
    Baxter MiniCap Extended Life PD Transfer Set (Easy-Lock), 5C4449
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0562-2022·2022-02-16

    Novalung Sensor Box Communication Failure May Disable Flow Measurement

    The Novalung Sensor Box may experience communication failures between its flow sensor and sensor box component, potentially disabling flow measurement and air bubble detection. The recall affects 115 units distributed across 16 US states.

    Product
    Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)- Indicated for long-term (> 6 hours) respiratory/ cardiopulmonary support that provides assisted extracorporeal circulation and physiologic gas exchange (oxygenation and CO2 removal) of the patient's blo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0602-2022·2022-02-16

    GE Healthcare MRI systems recalled for cryogen ventilation system defect

    GE Healthcare Discovery MR450 MRI systems may have cryogen ventilation systems that do not meet required venting standards. The recall affects approximately 17,228 devices distributed in the U.S. and internationally.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR450 1.5T 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-0584-2022·2022-02-16

    KWIK-STIK Quality Control Sets recalled for potential bacterial contamination

    Microbiologics Inc is recalling KWIK-STIK QC Sets and Panels due to potential contamination with E. coli and Staphylococcus species. The affected product was distributed worldwide to laboratory testing facilities.

    Product
    QC Sets and Panels: KWIK-STIK" 2 Pack. Common Name: QC Sets and Panels GP Comprehensive QC Set. Each KWIK-STIK unit contains a lyophilized microorganism pellet, an ampoule of hydrating fluid, and an inoculating swab. Each device is sealed within a laminated pouch that conta
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0635-2022·2022-02-16

    Acufex Access Advanced Positioning Kit Recalled for Missing Sterilization

    Smith & Nephew is recalling the Acufex Access Advanced Positioning Kit because the products were shipped to a distribution center instead of the sterilizer and were not sterilized before distribution.

    Product
    Acufex Access Advanced Positioning Kit - indicated for use to position and distract the extremity of patient during open and arthroscopic surgical procedures Product Number: 72205104
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0595-2022·2022-02-16

    GE Healthcare MR Magnets Cryogenic Ventilation System Defect Recall

    GE Healthcare is recalling 17,228 MR superconducting magnet systems because the cryogenic ventilation system may not meet required venting standards.

    Product
    GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA PET/MR System, tomographic imager combining emission computed tomography with nuclear magnetic resonance system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0690-2022·2022-02-16

    Dole Chopped Teriyaki Pineapple Kit recalled for potential Listeria contamination

    Dole Fresh Vegetables is recalling its 9.8oz Chopped Teriyaki Pineapple Kit due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide with specific Best if Used By dates.

    Product
    Dole 9.8oz Chopped Teriyaki Pineapple Kit Product UPC 071430001004
    Category
    Food
    Distribution
    36 states
  • HighFDA (Devices)·Z-0572-2022·2022-02-16

    Baxter MiniCap PD Transfer Sets Recalled Due to Damage from Cleaning Products

    Baxter Healthcare is recalling 344,190 units of MiniCap Extended Life PD Transfer Sets worldwide because certain cleaning products may cause the sets to leak or crack, potentially affecting patient dialysis treatment.

    Product
    Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short, 5C4483
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·22721·2022-02-10

    2022 Can-Am Outlander ATVs Recalled Due to Speedometer Crash Hazard

    BRP U.S. Inc. is recalling about 1,300 2022 Can-Am Outlander ATVs because the speedometer can display half the vehicle's true speed, creating a crash hazard. Consumers should stop using the vehicles and contact a Can-Am dealer for a free repair.

    Product
    2022 Can-Am Outlander ATVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22722·2022-02-10

    Serta Perfect Sleeper Mattresses Recalled for Fire Hazard

    Serta is recalling about 800 Perfect Sleeper mattresses because they fail to meet federal flammability standards, creating a fire hazard. No injuries have been reported.

    Product
    Serta® Perfect Sleeper® Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V076000·2022-02-10

    2022 Thor Motor Coach Motorhomes Rear Ladder Installation Defect Recall

    Thor Motor Coach is recalling 2022 ACE, Freedom Traveler, Hurricane, and Windsport motorhomes. The rear ladder may have been installed on the wrong side, which could break while in use and cause injury.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH ACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22078·2022-02-10

    WORX 13 Amp 1900 PSI Electric Pressure Washers Recalled for Hose Separation

    Positec USA is recalling about 17,630 WORX Brand 13 Amp 1900 PSI Electric Pressure Washers because the sprayer hose can separate from the spray wand during use, posing an impact injury hazard. Four minor injuries including cuts and bruises have been reported.

    Product
    WORX® Brand 13 Amp 1900 PSI Electric Pressure Washers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0463-2022·2022-02-09

    Medroxyprogesterone Acetate Injection Recalled for Sterility Assurance

    Ideal Specialty Apothecary is recalling Medroxyprogesterone Acetate Injection due to lack of assurance of sterility. The recall affects approximately 57,994 vials distributed nationwide.

    Product
    Medroxyprogesterone Acetate Injection, IM, 150 mg/mL, packaged in 1 ml Single Dose Vial, RX Only, Ideal Pharmacy, 2333 Morris Ave, Union, NJ 07083
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0530-2022·2022-02-09

    Baxter SIGMA Spectrum infusion pumps recalled for medication delivery failures

    Baxter is recalling 146,502 SIGMA Spectrum infusion pumps due to potential medication delivery failures that may occur without alerting clinicians. The issue is linked to administration set setup and occlusion alarm resolution.

    Product
    Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product code 35700BAX2.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0529-2022·2022-02-09

    Baxter Spectrum IQ Infusion Pumps Recalled Due to Potential Medication Delivery Failure

    Baxter Healthcare is recalling 241,304 Spectrum IQ infusion pumps due to potential medication delivery failure without user alert. The issue may occur during administration set setup or when occlusion alarms are not fully resolved.

    Product
    Baxter Spectrum IQ Infusion Pumps, Product code 3570009.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0550-2022·2022-02-09

    OXY-1 System Console Experiences Power Interruption During Use

    OXY-1 System consoles used during cardiac support procedures may experience power interruptions that disrupt patient therapy, potentially causing prolonged oxygen deprivation.

    Product
    OXY-1 System, Model Number 001-0500-001. Used during cardiopulmonary bypass. OXY-1 System consists of Console, Pump Drive, E Drive, and Pole Mount. The disposable Pump Lung Unit PLU part number 001-0400-100 is sold separately and is not part of this recall.
    Category
    Medical Device
    Distribution
    7 states
  • SevereFDA (Devices)·Z-0480-2022·2022-02-09

    COVID-19 Rapid Antigen Test Kit Distributed Without FDA Approval

    CovClear COVID-19 Rapid Antigen Test kits (284,575 units) were distributed nationwide without FDA marketing approval, clearance, or authorization. All lots are recalled.

    Product
    CovClear COVID-19 Rapid Antigen Test, ATG 900-031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0481-2022·2022-02-09

    COVID-19 Test Kits Recalled for Unauthorized FDA Marketing and Sale

    Empowered Diagnostics LLC recalled COVID-19 test kits (ImmunoPass, NAB 900-60) sold nationwide without FDA approval. Approximately 2,100 units were distributed without required marketing clearance or authorization.

    Product
    ImmunoPass , COVID-19 Neutralizing Antibody Test, NAB 900-60
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22071·2022-02-09

    Children's Nightgowns Recalled for Flammability Standards Violation

    AllMeInGeld children's nightgowns fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 3,900 units were sold on Amazon.com from October 2017 through June 2021.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0548-2022·2022-02-09

    INTEGRA SURFIX ALPHA Torx 10 Screwdriver Out of Specification Recalled

    Smith & Nephew recalls INTEGRA SURFIX ALPHA Screwdriver Torx 10 units because they are out of specification and may not mate properly with the Surfix Alpha Lock screw.

    Product
    INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND
    Category
    Medical Device
    Distribution
    Distributed nationwide