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.

44601–44625 of 50511

  • HighFDA (Devices)·Z-0109-2013·2012-10-31

    Westmed Recalls Arterial Blood Gas Kits Due to Alcohol Pad Contaminants

    Westmed is recalling ABG sampling kits because the included TRIAD alcohol pads may contain potential contaminants.

    Product
    Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 3 cc, w/Crickett 23g x 1" A Needle, 25U Balanced Heparin, part number: 3383-95, 3344-95, 3353-95. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0119-2013·2012-10-31

    Biomet 3i Recalls Dental Implants Due to Missing Internal Threading

    Biomet 3i is recalling 227 Osseotite Tapered Certain Implants because a small percentage are missing internal threading. The devices were distributed worldwide.

    Product
    Osseotite Tapered Certain Implant 5 X 10mm Model INT510 Biomet 3i Dental Implants are intended for surgical placement in the upper or lower jaw to provide a means for prosthetic attachment in single tooth restorations and in partially or fully edentulous spans with multiple…
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0128-2013·2012-10-31

    Terumo Sarns Modular Perfusion System 8000 Recalled for Power Malfunctions

    Terumo CVS is recalling 466 Sarns Modular Perfusion System 8000 units due to reported power distribution and battery back-up malfunctions.

    Product
    Perfusion System 8000, base 4 pump, 220V/240V safety monitor included The Sarns Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures…
    Category
    Medical Device
    Distribution
    42 states
  • HighCPSC·13020·2012-10-25

    Tricam Recalls Easy Reach Step Stools Due to Fall Hazard

    Tricam Industries is recalling approximately 84,000 Easy Reach step stools sold at The Home Depot because the top step can break, posing a fall hazard.

    Product
    Step Stool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13703·2012-10-25

    FLO Cycling Recalls Bicycle Wheel Rim Tape Due to Fall Hazard

    FLO Cycling is recalling about 800 units of yellow plastic rim tape sold with specific wheels because the tape can fail, causing inner tubes to burst and posing a fall hazard.

    Product
    Bicycle Wheel Rim Tape
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0261-2013·2012-10-24

    Spartan Central Kitchen Recalls Bulk Honeydew Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 3-pound bulk honeydew products manufactured between August 20 and September 10, 2012, due to possible Listeria contamination found during an FDA inspection.

    Product
    #232 Bulk Honeydew 232 3 pounds
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0092-2013·2012-10-24

    Osteotech Recalls Grafton and Xpanse Bone Graft Products Due to Sterility Concerns

    Osteotech Inc is recalling multiple lots of Grafton and Xpanse bone graft products because the sterility of the inner pouch surface may be compromised.

    Product
    Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product containing demineralized human bone tissue combined with inert additive to yield a demineralized bone matrix (DBM) allograft. It is intended for use as a bone graft extender, bone…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0208-2013·2012-10-24

    Spartan Central Kitchen Recalls Fruit Dip Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling 8-ounce pre-pack fruit dip manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #372 Fruit Dip - Pre-Pack 8 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0063-2013·2012-10-24

    ConMed Linvatec Recalls PressFT Sutures Due to Driver Tip Separation Risk

    ConMed Linvatec is recalling PressFT HI-FI Sutures because the driver tip may separate from the shaft after implant insertion.

    Product
    "***PressFT***2.6 w/ Two #1 (4 metric) Hi-Fi***Sutures***NP262***2009-02***CONMED LINVATEC 11311 CONCEPT BLVD LARGO, FL 33773-4908 USA*** To reattach soft tissue to bone in orthopedic surgical procedures
    Category
    Medical Device
    Distribution
    17 states
  • HighNHTSA·12V517000·2012-10-24

    Altec Recalls 2011-2012 CFD 1217 Wood Chippers Due to Blade Defect

    Altec is recalling 2011-2012 CFD 1217 wood chippers because blades may not meet hardness specifications, posing a risk of injury if they fail.

    Product
    ALTEC — ALTEC CFD 1217 WOOD CHIPPER
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0267-2013·2012-10-24

    Spartan Central Kitchen Recalls Pineapple Products Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling specific pineapple products manufactured in August and September 2012 due to possible Listeria contamination found during an FDA inspection.

    Product
    #067 Fruit Cup: Pineapple Chunks 9 ounces #054 Cored Pineapple 16 ounces #076 Fruit Cup: Pineapple Chunks 15.8 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0259-2013·2012-10-24

    Spartan Central Kitchen Recalls Watermelon Products Due to Listeria Contamination

    Spartan Central Kitchen is voluntarily recalling bulk and tray watermelon products manufactured between August 20 and September 10, 2012, due to possible Listeria contamination found during an FDA inspection.

    Product
    #234 Bulk Watermelon 234 2.5 pounds and #050 Watermelon Tray 16 ounces
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0160-2013·2012-10-24

    Spartan Central Kitchen Recalls Garden Fresh Salads for Listeria Risk

    Spartan Central Kitchen is voluntarily recalling Garden Fresh salads due to possible Listeria contamination found during an FDA inspection.

    Product
    #762 Salad - Large Garden Fresh 3/4 pounds #761 Salad - Small Garden Fresh 3 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0274-2013·2012-10-24

    Spartan Central Kitchen Recalls Sugar Snap Peas Due to Listeria Risk

    Spartan Central Kitchen is voluntarily recalling 7-ounce Sugar Snap Peas in Michigan and Ohio due to possible Listeria contamination found during an FDA inspection.

    Product
    #033 Sugar Snap Peas 7 ounces
    Category
    Food
    Distribution
    2 states