The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

19601–19625 of 50413

  • HighFDA (Devices)·Z-2273-2021·2021-08-18

    Biomet Hip Implant System Recalled Due to Potential Fretting Corrosion

    Biomet is recalling the Arcos Modular Revision Hip System component due to potential inner taper fretting corrosion that could lead to device failure requiring surgery. No injuries have been reported.

    Product
    Arcos Modular Revision Hip System Standard Cone Prox Body, Size B, 80 MM Item Number: 11-301342
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2247-2021·2021-08-18

    Jamshidi Bone Marrow Biopsy Needles Recalled for Packaging Seal Defects

    Bard Peripheral Vascular Inc. is recalling multiple models of Jamshidi bone marrow biopsy needles due to incomplete or open packaging seals that may compromise sterility. No illnesses or injuries have been reported.

    Product
    TJM6008 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 8G x 15 cm; TJC3513 Jamshidi" Bone Marrow Biopsy/Aspiration Needle. 13G x 8.9 cm; TJM4011 Jamshidi" Crown Bone Marrow Biopsy/Aspiration Needle with Marrow Acquisition Cradle. 11G x…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0857-2021·2021-08-18

    5000 Years Foods Baby Napa Kimchi Recall for Listeria Contamination

    5000 Years Foods is recalling Baby Napa Kimchi in 128 oz, 64 oz, and 32 oz glass jars due to potential contamination with Listeria monocytogenes. The product was distributed in Illinois and potentially nationwide through retail distributors.

    Product
    5000 Years Foods BABY NAPA KIMCHI in 128 oz, 64 oz, and 32 oz glass jars
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21182·2021-08-18

    B-Air VP-33 Blower Fans Recalled Due to Fire Hazard

    Intertex is recalling about 29,500 B-Air VP-33 blower fans because the capacitor can overheat and pose a fire hazard. The firm has received five reports of fire-related property damage totaling about $75,000, though no injuries have been reported.

    Product
    B-Air VP-33 Blower Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2223-2021·2021-08-18

    Stryker GoBed II Medical Bed Recalled for Improper Home Distribution

    Stryker's GoBed II MedSurg Bed was distributed to residential customers but is intended for healthcare facility use. Home users may not understand professional-level safety instructions, creating a risk of misuse.

    Product
    GoBed II MedSurg Bed, Model Number FL28, Part #FL28EX
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0854-2021·2021-08-18

    5000 Years Foods Kimchi Recalled for Listeria Contamination Risk

    5000 Years Foods is recalling NO MSG JULRADO WHOLE CABBAGE KIMCHI in 128 oz and 64 oz glass jars due to potential Listeria monocytogenes contamination. The affected product was distributed through Illinois and reached customers nationwide.

    Product
    5000 Years Foods NO MSG JULRADO WHOLE CABBAGE KIMCHI in 128 oz and 64 oz glass jars
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0856-2021·2021-08-18

    5000 Years Foods White Whole Kimchi Recall Due to Listeria Risk

    5000 Years Foods is recalling White Whole Kimchi in 32 oz, 64 oz, and 128 oz glass jars due to potential Listeria monocytogenes contamination. The affected product was distributed through Illinois to retail locations potentially nationwide.

    Product
    5000 Years Foods WHITE WHOLE KIMCHI in 128 oz, 64 oz, and 32 oz glass jars
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2280-2021·2021-08-18

    Edwards PediaSat Oximetry Catheter Kits Recalled for Potential Internal Leaks

    Edwards Lifesciences is recalling PediaSat Oximetry Catheter Kits due to potential internal leaks within the devices. The recall involves 218 units distributed across multiple U.S. states and internationally.

    Product
    Edwards PediaSat Oximetry Catheter Kit, REF: XT358SJ, Usable Length 8 cm, Number of Lumens 3, Exterior Diameter 5.5F, Rx Only, Sterile EO, UDI: (01)00690103197495 *NOT DISTRIBUTED WITHIN THE US
    Category
    Medical Device
    Distribution
    12 states
  • HighNHTSA·21V643000·2021-08-17

    Swab Wagon Recalls Medic Vehicles with Excessively Bright LED Lights

    Swab Wagon is recalling 2017-2019 Chevrolet and Ford medic vehicles because their LED lights are too bright, potentially blinding other drivers and increasing crash risk.

    Product
    SWAB WAGON — SWAB WAGON CHEVROLET 3500, FORD F-350, CHEVROLET 2500 HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E075000·2021-08-17

    Cummins Recalls Generator Sets Due to Improperly Crimped Lifting Cables

    Cummins is recalling specific generator sets because lifting cables may be improperly crimped. This defect could cause the equipment to fall during lifting, increasing the risk of injury.

    Product
    EQUIPMENT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V645000·2021-08-17

    Kibbi Recalls 2019-2021 Renegade Vienna and Villagio RVs for Fire Risk

    Kibbi, LLC is recalling 2019-2021 Renegade Vienna and Villagio recreational vehicles because exhaust heat may cause the storage box to melt or catch fire.

    Product
    RENEGADE — RENEGADE VILLAGIO, VIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V642000·2021-08-17

    Newmar motorhomes recalled for fuel hose leak fire risk

    Newmar is recalling 2021-2022 motorhomes with Cummins L9 diesel engines due to a potential fuel leak from a fuel hose that could cause fire.

    Product
    NEWMAR — NEWMAR VENTANA, NEW AIRE, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V641000·2021-08-16

    Alexis Fire Equipment Recalls 2015-2020 Fire Apparatus Due to Bright Lights

    Alexis Fire Equipment is recalling 2015-2020 emergency vehicles because LED lights may be too bright, potentially affecting driver vision and increasing crash risk.

    Product
    ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V640000·2021-08-15

    Ferrara Recalls One 2020 Igniter Emergency Vehicle for Display Defect

    Ferrara Fire Apparatus is recalling one 2020 Igniter emergency vehicle because the instrument cluster display may lock up or become nonfunctional due to low voltage spikes.

    Product
    FERRARA — FERRARA IGNITER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V639000·2021-08-13

    Mercedes-Benz Recalls 2020 GLB 250 for Air Bag Software Defect

    Mercedes-Benz is recalling 2020 GLB 250 vehicles because air bag control software may prevent front seat belts and air bags from activating properly in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLB 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V638000·2021-08-13

    Mercedes-Benz Recalls Vehicles Due to Incorrect Front Passenger Air Bag

    Mercedes-Benz is recalling specific 2011-2016 models because an incorrect front passenger air bag may have been installed during a prior repair, potentially failing to function in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C250, E350, AMG C63, C350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V636000·2021-08-13

    2021 Grand Design Imagine trailers recalled for incorrect axle bearings

    Grand Design is recalling certain 2021 Imagine recreational trailers with Dexter D30 axles due to incorrect inner bearings. The bearings can cause wheels to lock or reduce stopping ability, increasing crash risk.

    Product
    GRAND DESIGN — GRAND DESIGN IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21774·2021-08-12

    YOH Super Soft Purple Rugs Recalled Due to Fire Hazard

    About 100 YOH Super Soft Purple Rugs sold on Amazon.com fail to meet federal flammability standards, posing a fire hazard. Consumers should stop using them immediately.

    Product
    YOH Super Soft Purple Rugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21773·2021-08-12

    Rossignol All Track DH Bicycles Recalled Due to Fall Hazard

    Rossignol is recalling 2018 and 2019 model year All Track DH bicycles because cracks can form at the head tube weld, causing the fork and front wheel to separate from the frame during use and create a fall hazard.

    Product
    Rossignol 2018 and 2019 Model Year All Track DH Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V632000·2021-08-12

    RAM Trucks Recalled for Side Air Bag Inflator Defect

    Chrysler is recalling 2015-2020 RAM trucks because side air bag inflators may rupture or detach, posing an injury risk.

    Product
    RAM — RAM 2500, 3500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2185-2021·2021-08-11

    Abbott Activated Alanine Aminotransferase Reagent Recalled for Inaccurate Test Results

    Abbott is recalling 1,603 units of its Activated Alanine Aminotransferase (A-ALT) lab reagent due to potential inaccuracies in test results. High bilirubin or high A-ALT samples may produce incorrect results affecting patient care.

    Product
    REF 8L92-22, Abbott Activated Alanine aminotransferase, for use with Architect, IVD, CE, UDI: (01) 00380740161859
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2179-2021·2021-08-11

    Sterile Home Artificial Insemination Kits Recalled for Missing FDA Marketing Authorization

    Tenderneeds Fertility LLC is recalling sterile home artificial insemination semen kits distributed worldwide prior to December 9, 2019, due to lack of required FDA marketing authorization.

    Product
    2 X Sterile Human Home Artificial Insemination Semen Kit (Human), SKU 143298592960
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0829-2021·2021-08-11

    Freshness Guaranteed Chocolate Chip Mini Muffins Recalled for Listeria Risk

    Freshness Guaranteed Chocolate Chip Mini Muffins are being recalled due to potential Listeria monocytogenes contamination. Affected units have specific lot codes and were distributed nationwide.

    Product
    Freshness Guaranteed Chocolate Chip Mini Muffins - 12 oz., 10 per case; UPC: 078742-08935 5
    Category
    Food
    Distribution
    Distributed nationwide