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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25226–25250 of 26084

  • SevereFDA (Devices)·Z-2017-2021·2021-07-21

    VITALIO DR EL Pacemakers Recalled Due to Battery-Related Device Resets

    Boston Scientific is recalling VITALIO DR EL pacemakers with Extended Life batteries due to a latent battery condition that may cause unexpected device resets and Safety Mode activation later in device life.

    Product
    VITALIO DR EL (pacemaker), Model Numbers: a) J274 b) J277 c) K274 (added 7/15/2021) d) K277 (added 7/15/2021) e) K284 (added 7/15/2021) f) K287 (added 7/15/2021)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0779-2021·2021-07-21

    Living Free Lung & Joint Congestion Herbal Dietary Supplement Soy Allergen

    Bea Lydeckers Naturals Inc is recalling Living Free Lung & Joint Congestion Herbal Dietary Supplement because the label declares lecithin but does not identify it as soy lecithin, creating an undeclared soy allergen hazard.

    Product
    Living Free Lung & Joint Congestion Herbal Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Lung & Joint Congestion Herbal Dietary Supplement***Glandular,
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V554000·2021-07-21

    2021 BMW X2 Seat Belt Retractor Defect Increases Injury Risk

    BMW is recalling certain 2021 X2 vehicles because the passenger seat belt retractor may deactivate early, failing to comply with federal safety standards. The defective retractor could increase injury risk in a crash.

    Product
    BMW — 2021 BMW X2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2076-2021·2021-07-21

    Medtronic LINQ II Insertable Cardiac Monitor Detection Failure Recall

    Medtronic is recalling the LINQ II Model LNQ22 Insertable Cardiac Monitor because it may fail to detect dangerous heart rhythms after a restart. The device was distributed worldwide.

    Product
    Medtronic LINQ II Model Number # LNQ22 Insertable Cardiac Monitor Sterile EO Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V555000·2021-07-21

    2021 Nissan Rogue Sport Seat Belt Retractor Safety Defect Recall

    Nissan is recalling 2021 Rogue Sport vehicles because seat belt automatic locking retractors may deactivate prematurely, reducing protection for child safety seats and violating federal crash protection standards.

    Product
    NISSAN — 2021 NISSAN ROGUE SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2025-2021·2021-07-21

    Shoulder prosthesis component distributed with incorrect thickness due to lot swap

    Two lots of Aequalis Ascend Flex Shoulder System Reversed Tray components were swapped during distribution, resulting in packages containing components with incorrect thickness.

    Product
    Aequalis Ascend Flex Shoulder System Reversed Platform (Reversed Tray component) Rx Only Sterile Manufacturer Tornier SAS - Saint Martin, France. Shoulder prosthesis component.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2050-2021·2021-07-21

    EcoFit Cementless Acetabular Cup Plugs May Loosen During Hip Surgery

    Central hole cover plugs on EcoFit cementless acetabular cups may come loose during surgical implantation, potentially extending operation time or requiring revision surgery. Fifty-one units in Florida and Texas are affected.

    Product
    EcoFit cup cementless: Model(Catalog Number)/Description: 02200046 /EcoFit cup cementless 46mm dia incl. central hole cover; 02200048 /EcoFit cup cementless 48mm dia incl. central hole cover; 02200050 /EcoFit cup cementless 50mm dia incl. central hole cover; 02200052 /EcoFit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2064-2021·2021-07-21

    MRI System Patient Orientation Button May Cause Flipped Images

    GE Healthcare's Discovery MR450 1.5T MRI system may inadvertently change patient orientation when users click the wrong button, resulting in flipped or incorrectly annotated images that could affect diagnostic accuracy.

    Product
    Discovery MR450 1.5T, Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0778-2021·2021-07-21

    Living Free Immune Dietary Supplement Soy Allergen Mislabeling Recall

    Bea Lydeckers Naturals Inc is recalling Living Free Immune Dietary Supplement because the label declares lecithin but does not declare that it contains soy lecithin, posing a risk to consumers with soy allergies.

    Product
    Living Free Immune Dietary Supplement, 100 and 500 capsules per bottles. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Immune Dietary Supplement***Glandular and Herbal Supplement***Formulated by Beatrice Ly
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0776-2021·2021-07-21

    Living Free Adult Extra Multi-Vitamin Recall for Undeclared Soy

    Bea Lydeckers Naturals Inc is recalling Living Free "Adult Extra" multi-vitamin capsules because the label declares lecithin but does not declare that it is soy lecithin, posing a risk to consumers with soy allergies.

    Product
    Living Free "Adult Extra" multi-vitamin, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "**Living Free Adult Extra***Natural Vitamin Mineral Herbal Glandular Supplements***Formulated and Manu
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21167·2021-07-21

    Caldwell E-Max Pro BT Earmuffs Recalled for Fire and Burn Hazards

    American Outdoor Brands is recalling Caldwell E-Max Pro BT Earmuffs with rechargeable lithium battery packs due to a soldering defect that can cause the unit to overheat, posing fire and burn hazards. No injuries have been reported.

    Product
    Caldwell E-Max® Pro BT Earmuffs with rechargeable lithium battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2063-2021·2021-07-21

    MRI System Patient Orientation Button Click Error May Flip Images

    GE Healthcare is recalling 1,519 Optima MR450w MRI systems worldwide due to a button interface error. The 'Patient Orientation' button may be unintentionally clicked instead of 'Save RX,' causing incorrectly oriented or flipped diagnostic images.

    Product
    Optima MR450w 1.5T, Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0777-2021·2021-07-21

    Living Free Heart/Blood Vessel Dietary Supplement Recalls for Undeclared Soy

    Bea Lydeckers Naturals Inc is recalling Living Free Heart/Blood Vessel Dietary Supplement because the label declares lecithin but does not declare that it is soy lecithin, posing a risk to consumers with soy allergies.

    Product
    Living Free Heart/Blood Vessel Dietary Supplement, 100 or 500 capsules per bottle. Product is packed in white, HDPE plastic bottles with threaded HDPE lids. Label is read in parts: "***Living Free Heart/Blood Vessel Dietary Supplement***Glandular Herbal & Vitamin Blend***F
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2078-2021·2021-07-21

    Unifine Pentips Plus pen needles distributed with incorrect needle sizes

    Owen Mumford USA is recalling Unifine Pentips Plus pen needles because two cases of 4mm needles were mistakenly packaged as 8mm needles, which could result in patients receiving incorrect needle sizes for their insulin pens.

    Product
    Unifine Pentips Plus, hypodermic needle - Product Usage: Pen needles with built in pen needle remover.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2044-2021·2021-07-21

    Toshiba Vantage MRI System Recalled for Flame Retardancy Defect

    Canon Medical's Toshiba Vantage Tiitan 1.5T MRI systems are being recalled due to a component that does not meet flame retardancy standards. The defect could result in smoke or fire. Affected units were distributed nationwide.

    Product
    Toshiba Vantage Tiitan 1.5T with Standard gradient, Premium Open-Bore MRI System, REF: MRT-1504 - Product Usage: use as a diagnostic imaging modality that produces cross-sectional transaxial, coronal, sagittal, and oblique images that display anatomic structures of the head or bo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0691-2021·2021-07-21

    Limar Hand Sanitizer recalled for deceptive container packaging

    Limar Hand Sanitizer (70% isopropyl alcohol) in 4 oz bottles is being recalled because the containers resemble drinking water bottles, creating a risk of accidental ingestion.

    Product
    Limar Hand Sanitizer, Isopropyl Alcohol 70%, Cont. 4 oz bottles, Manufactured in Dominican Republic: by Ardil Comercial S.R.L., Santo Domingo, Dominican Republic UPC 7 487040 301587
    Category
    Drug
    Distribution
    0 states
  • HighFDA (Devices)·Z-2068-2021·2021-07-21

    Arrow Pacing Catheter Kit Recalled for Missing FDA Premarket Clearance

    Arrow International is recalling the Pacing Catheter Kit-Bipolar Electrode Catheter (48 units) due to marketing without required FDA premarket clearance (510K). Units were distributed nationwide in FL, ID, IL, NY, OH, and TX.

    Product
    Arrow Pacing Catheter Kit-Bipolar Electrode Catheter 5 Fr. 110 cm, Product Code: AI-05210 - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2072-2021·2021-07-21

    HeartWare HVAD Pump Implant Kit Impeller Defect Recall

    HeartWare HVAD Pump Implant Kit (REF MCS1705PU) recalled because the pump's impeller shroud height does not meet the lower control limit. The device is used for hemodynamic support in patients with advanced heart failure.

    Product
    HeartWare, HVAD Pump Implant Kit, REF MCS1705PU - Product Usage: indicated for hemodynamic support in patients with advanced, refractory left ventricular heart failure; either as a Bridge to Cardiac Transplantation (BTT), myocardial recovery, or as Destination Therapy (DT) in pat
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2048-2021·2021-07-21

    Hang&Go Hyperthermic Perfusion Kit Recall Due to Sterilization Failure

    RanD S.r.l. is recalling Hang&Go hyperthermic perfusion kits due to a sterilization process failure that may have left some units non-sterile. The recall affects 72 kits distributed to Florida, Illinois, Tennessee, and Wisconsin.

    Product
    Hang&Go (kit for hyperthermic perfusion), Reference Code R9900120
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-2058-2021·2021-07-21

    MRI Imaging System UI Defect May Cause Incorrect Image Orientation

    GE Healthcare recalled 1,737 SIGNA Creator and SIGNA Explorer MRI systems due to a software bug where the 'Patient Orientation' button can be accidentally clicked instead of 'Save RX,' potentially causing incorrectly oriented diagnostic images.

    Product
    SIGNA Creator, SIGNA Explorer, Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2070-2021·2021-07-21

    Arrow Bipolar Balloon Electrode Catheter Recalled for Marketing Without FDA 510K Clearance

    Arrow International is recalling 4 units of an electrode catheter marketed without FDA 510(k) clearance. The device was intended for electrophysiology studies.

    Product
    Arrow Bipolar Balloon Electrode Catheter 5 Fr. 105 cm, Product Code: AI-07154 - Product Usage: intended for temporary use in electrophysiology studies for intracardiac stimulation and/or ECG recording.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2055-2021·2021-07-21

    MRI Scanner Patient Orientation Button Confusion Affects Images

    GE Healthcare's MRI scanners may have a button confusion issue where the Patient Orientation button is accidentally clicked instead of Save RX, potentially causing misoriented or incorrectly annotated images. 585 devices affected worldwide.

    Product
    Discovery MR750w 3.0T - Product Usage: is a whole body magnetic resonance scanner designed to support high resolution, high signal-to-noise ratio, and short scan times.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2075-2021·2021-07-21

    Medical device software c4D fails to change site upon synchronization

    C-RAD POSITIONING AB is recalling Catalyst positioning software c4D because it fails to properly update the Site field during synchronization in the setup workflow. This software defect may prevent correct system configuration.

    Product
    PC Application Software c4D as part of the device Catalyst: SP-002 Software PA-003 version 6.1.1 and 6.1.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0773-2021·2021-07-21

    Watson Pickled Garlic Ail Marine Recalled for High Lead Levels

    Watson Pickled Garlic Ail Marine (500g pouches) is being recalled because 40 cases containing high lead levels were distributed despite FDA detention.

    Product
    Watson Pickled Garlic Ail Marine; 500g (18 oz. plastic pouch. Refrigerate after opening. UPC 8 00794 00303 0
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0775-2021·2021-07-21

    Caribbean Belize Spices Caribbean Rub Recalled for Undeclared Wheat

    Caribbean Belize LLC is recalling Caribbean Rub spice bottles because they contain undeclared wheat, which poses a risk to consumers with wheat allergies or celiac disease.

    Product
    Caribbean Belize Spices Caribbean Rub, Net Wt. 3.5oz (99g) Plastic bottle with black cap Sold as single bottles
    Category
    Food
    Distribution
    6 states