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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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

25051–25075 of 26084

  • SevereFDA (Devices)·Z-2157-2021·2021-08-04

    Zippie Voyage Early Intervention Stroller Seating System May Detach

    Sunrise Medical recalls Zippie Voyage early intervention strollers because the seating system may unexpectedly detach and fall, causing injury. Approximately 9,865 devices are affected.

    Product
    Zippie Voyage, early intervention stroller - Product Usage: is manually operated by a caregiver for purposes of assisting a disabled person while providing supportive elements for assisted transportation and seating for a child or small adult not to exceed 75 pounds.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0863-2021·2021-08-04

    Old Souls Farm Finstar Microgreens Recalled for Listeria Contamination

    Old Souls Farms LLC is recalling Finstar microgreens distributed to Ohio and Kentucky due to positive testing for Listeria monocytogenes in rainwater that contacted the product.

    Product
    Old Souls Farm Finstar 5 oz clamshells - 1oz 18 per case, 5oz 6 per case bulk bags - 1lb is 3 per case, 10lbs 1 per case, 25lbs 1 per case living are packed in plastic sleeves - 10 per case
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0805-2021·2021-08-04

    Randall Ultimate 4-Bean Mix Recalled for Lack of Temperature Indicators

    Randall Foods, Inc. is recalling Randall Ultimate 4-Bean Mix in 48 oz glass jars due to non-functioning temperature indicating devices in retorts used during processing, which may affect proper sterilization.

    Product
    RANDALL ULITMATE 4-BEAN MIX 48OZ glass jars UPC 070095000902
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0799-2021·2021-08-04

    Randall Pinto Beans Recall Due to Temperature Control Defect

    Randall Foods, Inc. is recalling Randall Pinto Beans in three sizes (48oz, 24oz, and 15.4oz glass jars) distributed across 22 states due to lack of functioning temperature-indicating devices in retorts used during processing.

    Product
    RANDALL PINTO BEANS 48OZ glass jars UPC 070095000209; RANDALL PINTO BEANS 24OZ glass jars UPC 070095000216; RANDALL PINTO BEANS 15.4OZ glass jars UPC 070095000230
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0801-2021·2021-08-04

    Randall Kidney Beans Recall for Faulty Temperature Devices

    Randall Foods, Inc. is recalling Randall Kidney Beans in three sizes due to non-functioning temperature indicating devices in retorts, which may affect proper heat sterilization during processing.

    Product
    RANDALL KIDNEY BEANS 48OZ glass jars UPC 070095000308; RANDALL KIDNEY BEANS 24OZ glass jars UPC 070095000315; RANDALL KIDNEY BEANS 15.4OZ glass jars UPC 070095000339
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0864-2021·2021-08-04

    Old Souls Farm Green Bibb Lettuce Recalled for Listeria Risk

    Old Souls Farms LLC is recalling Green Bibb lettuce products distributed to Ohio and Kentucky due to rainwater testing positive for Listeria monocytogenes that came into contact with the product.

    Product
    Old Souls Farm Green Bibb 2 lbs, 5 oz, Living Heads clamshells - 1oz 18 per case, 5oz 6 per case bulk bags - 1lb is 3 per case, 10lbs 1 per case, 25lbs 1 per case living are packed in plastic sleeves - 10 per case
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0795-2021·2021-08-04

    Backcountry Dried Apricots Recalled for Undisclosed Sulfites

    Lipari Foods Operating Company is recalling Backcountry Dried Apricots due to sulfites not being disclosed on the product label. The product was distributed to retail locations across 18 states.

    Product
    Backcountry Dried Apricots 9ounce plastic bag 12 packages per case
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-0802-2021·2021-08-04

    Randall Navy Beans recalled due to non-functioning temperature devices

    Randall Foods is recalling Randall Navy Beans in 48 oz and 15.4 oz glass jars due to lack of functioning temperature indicating devices in retorts during processing.

    Product
    RANDALL NAVY BEANS 48OZ glass jars UPC 070095000506; RANDALL NAVY BEANS 15.4OZ glass jars UPC 070095000537
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2164-2021·2021-08-04

    Semi-automatic Biopsy Needles Recalled Due to Sterilization Defect

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling semi-automatic biopsy needles because labeled sterile units may not have been adequately sterilized. Affected devices distributed in California should not be used.

    Product
    Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. BIM 18/10, Length 100 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/15, Length 150 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/20, Length 200 mm, Diameter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2138-2021·2021-08-04

    RayStation radiation treatment planning system positioning error recall

    RayStation versions 9A through 11A may set initial delivery positions incorrectly during setup beam localization. Five units are affected; no patient injuries reported.

    Product
    RayStation (Radiation Treatment Planning System) : RayStation 9A, 9B, 9B SP1, 10A, 10A SP1, 10B and 11A, in combination with RayCare Model Numbers/ UDI: RayStation 9.0 (9.0.0.113) 07350002010174; RayStation 9.1 (9.1.0.933) 07350002010266; RayStation 9.1 Service Pack 1 (
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2160-2021·2021-08-04

    OEC 3D Imaging X-Ray Systems Recalled for Coin Cell Battery Depletion

    GE OEC Medical Systems is recalling certain OEC 3D Imaging fluoroscopic X-ray systems due to potential premature depletion of the coin cell battery used to monitor X-ray tube temperature, which could cause the system to become inoperable.

    Product
    OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic and digital spot images of adult and pediatric populations during diagnostic, interventional, and surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0807-2021·2021-08-04

    Choujuki White Bread recalled for undeclared milk allergen

    Choujuki White Bread (6 slices, 13.9 oz) is being recalled because labeling failed to declare milk as an allergen. The milk is a sub-ingredient of the margarine used in the product.

    Product
    Choujuki White Bread 6 slices: Net Wt. 13.9 oz. (374g) Ingredients: White Flour, Sugar, Margarine, Yeast Extract, Salt, Rice Flour, Vinegar. Contains Wheat. Keep Frozen at or below 18 degrees C Distributed by Hatsune JPN Inc., Torrance, CA Product of Japan/
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0797-2021·2021-08-04

    Amy's Tortilla Casserole Bowls Recalled for Rubber Gasket Pieces

    Amy's Kitchen is recalling Amy's Bowls Tortilla Casserole & Black Beans due to the potential presence of rubber gasket pieces from production equipment. Consumers should not eat the product and should dispose of it or return it to the store.

    Product
    Amy's Bowls, Tortilla Casserole & Black Beans; Made with organic tomatoes & Black Beans. NET WT 9.5 oz. (269g); gluten Free - Perishable - keep frozen; UPC: 0 42272 00168 2 (individual box) Case UPC: 1-00-42272-00168-9 Microwave or regular oven. In trays with plastic overlay, in
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-2147-2021·2021-08-04

    CooperVision CLARITI Contact Lenses Recalled for Misaligned Axis Marks

    CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot U0108940) because misaligned axis marks can cause blurred vision in patients.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2137-2021·2021-08-04

    Infusomat Space Pump Administration Set Recalled for Inverted Anti-Free Flow Clip

    B. Braun Medical is recalling the Infusomat Space Volumetric Pump Administration Set due to a defect where the anti-free flow clip may be inverted, potentially causing unintended medication flow. No injuries have been reported.

    Product
    Infusomat Space Volumetric Pump Administration Set, Product Code 490100
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-2145-2021·2021-08-04

    Contact lens recall due to misaligned axis marking

    CooperVision Inc. is recalling FRESH DAY 1 DAY TORIC contact lenses (Lot R0121629) due to misaligned axis marks that may cause blurred vision in wearers.

    Product
    FRESH DAY 1 DAY TORIC Power -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2161-2021·2021-08-04

    OEC Elite Mobile C-Arm Recalled for Battery Depletion

    GE OEC Medical Systems is recalling 3,570 OEC Elite mobile C-arm imaging systems worldwide due to potential early depletion of the battery that monitors X-ray tube temperature, which could render the system inoperable.

    Product
    OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2134-2021·2021-08-04

    Diagnostic Genetic Probe Recalled for Unexpected Chromosome Signals

    Cytocell Ltd. is recalling CytoCell DiGeorge/VCFS genetic probes that may display unexpected chromosome signals, potentially causing misdiagnosis. Affected reagents were distributed to laboratories in multiple US states and Canada.

    Product
    CytoCell DiGeorge/VCFS TUPLE1 Region and 22q13.3 Region Probe, Model Number LPU004-A. analyte specific reagent for in vitro diagnostics
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-2146-2021·2021-08-04

    CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis mark misalignment

    CooperVision is recalling CLARITI 1 DAY TORIC daily disposable contact lenses due to misaligned axis marks that can cause blurred vision. Affected lenses in lot U0108833 were distributed in seven US states and internationally.

    Product
    CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V604000·2021-08-04

    Newmar Motorhomes Recalled for Potential Fuel Leak and Fire Risk

    Newmar Corporation is recalling certain 2021-2022 motorhomes (New Aire, Ventana, and Dutch Star) with Cummins L9 diesel engines due to potential fuel leaks that could increase fire risk. Affected owners should contact Newmar customer service at 1-800-731-8300 for free fuel hose replacement.

    Product
    NEWMAR — 2022 NEWMAR NEW AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2156-2021·2021-08-04

    Affinity Four Birthing Bed Latch Mechanism Defect Poses Fall Risk

    The latch mechanism on the Lift-Off foot section of certain Affinity Four Birthing Beds may be damaged, potentially causing improper engagement and creating a fall risk for patients. Hill-Rom is recalling approximately 1,096 affected beds.

    Product
    Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2163-2021·2021-08-04

    Coaxial Interventional Needles recalled for potential sterilization failure

    Coaxial Interventional Needles from INNOVATIVE TOMOGRAPHY PRODUCT GMBH may not be properly sterilized. Multiple lot numbers are affected and should not be used.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIR 23/05, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/05N, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/07, Length 75 mm, Diameter 2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2162-2021·2021-08-04

    Coaxial Interventional Needles Recalled for Potential Sterilization Defects

    INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling Coaxial Interventional Needles distributed in California due to potential sterilization defects. Needles labeled as sterile may not have been adequately sterilized, creating infection risks.

    Product
    Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIM 22/05, Length 50 mm, diameter 22G/0,7 mm; Article no. KIM 22/07,Length 75 mm, diameter 22 G (0.7 mm); Article no. KIM 22/10, Length 100 mm, diameter 22 G
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2155-2021·2021-08-04

    Proteus 235-Proton Therapy System May Deliver Unintended Radiation

    The Proteus 235-Proton Therapy System may deliver proton therapy without prescribed beam gating if the user forgets to select the trigger input. This could cause radiation to be positioned incorrectly.

    Product
    Proteus 235-Proton Therapy System
    Category
    Medical Device
    Distribution
    5 states