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.

45226–45250 of 50512

  • HighFDA (Food)·F-1553-2012·2012-08-15

    River Ranch Italian Salad Recalled for Listeria Contamination

    River Ranch Fresh Foods is recalling Italian Salad bags after FDA samples tested positive for Listeria monocytogenes.

    Product
    River Ranch brand Italian Salad, 10 oz bag, UPC: 45388-60020;Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product is processed and packaged by River Ranch Fresh…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2181-2012·2012-08-15

    Kimberly-Clark Patient Warming System Recalled for Fuse Holder Defect

    Kimberly-Clark is recalling 129 Model 1000 Patient Warming System Control Units because a fuse holder defect may cause the device to fail or generate smoke.

    Product
    Kimberly Clark Patient Warming System - Model 1000 Control Unit. Kimberly Clark Patient Warming System - Model 1000 Control Unit and Energy Transfer Pads is a thermal regulating system, indicated for monitoring and controlling patient temperature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1558-2012·2012-08-15

    River Ranch Heritage Blend Salad Recalled for Listeria Contamination

    River Ranch Fresh Foods is recalling Heritage Blend salad due to Listeria monocytogenes contamination found in FDA-pulled samples.

    Product
    River Ranch brand Heritage Blend, 16 oz bag, UPC: n/a; Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product is processed and packaged by River Ranch Fresh Foods…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2172-2012·2012-08-15

    Siemens EasyLink Informatics System Recalled for Incorrect Diagnostic Results

    Siemens Healthcare Diagnostics is recalling 237 EasyLink Informatics Systems because they may display and transmit incorrect results to Laboratory Information Systems when used with specific coagulation analyzers.

    Product
    EasyLink(TM) Informatics System, Part Number 1000034805. EasyLink(TM) Informatics System is classified as a data calculator and processing module for use with In-Vitro diagnostics devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2158-2012·2012-08-15

    Biomet 3i Recalls Dental Implants Due to Shallow Internal Hex Depth

    Biomet 3i is recalling specific dental implants because the internal hex depth is too shallow, which may prevent components from fully engaging the implant.

    Product
    ***REF IFNT611***Full OSSEOTITE Tapered Certain Implant 6 x 11.5mm***Sterile by radiation***Rx Only***BIOMET 3i Dental Iberica S.L. WTC Almeda Park, Ed, 1, Planta 1 Pl. de la Pau s/n08940 Cornella de Llobregat (Barcelona) Spain. Lot #2011110798. Intended for surgical…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1545-2012·2012-08-15

    River Ranch Angel Hair Salad Recalled for Listeria monocytogenes

    River Ranch Fresh Foods is recalling Angel Hair salad due to Listeria monocytogenes contamination found in FDA samples.

    Product
    River Ranch brand Angel Hair, 10 oz bag, UPC: 45388-10031;Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product is processed and packaged by River Ranch Fresh Foods…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1557-2012·2012-08-15

    River Ranch Spring Mix Recalled for Listeria monocytogenes Contamination

    River Ranch Fresh Foods is recalling Spring Mix salad bags because FDA samples tested positive for Listeria monocytogenes.

    Product
    River Ranch brand Spring Mix, 24 oz bag, 48 oz bag, UPCs: n/a; Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product is processed and packaged by River Ranch Fresh…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1616-2012·2012-08-15

    River Ranch Recalls Fresh n Easy Shredded Green Cabbage Due to Listeria

    River Ranch Fresh Foods is recalling Fresh n Easy brand shredded green cabbage because samples tested positive for Listeria monocytogenes.

    Product
    Fresh n Easy brand Shred Grn Cabbage w/Color, 4 x 5 lb bag, UPC: n/a; Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product is processed and packaged by River Ranch…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1585-2012·2012-08-15

    River Ranch Garden Salad Recalled Due to Listeria Contamination

    River Ranch Fresh Foods is recalling The Farmers Market brand Garden Salad because samples tested positive for Listeria monocytogenes.

    Product
    The Farmers Market brand Garden Salad, 6 oz, 12 oz, 24 oz bags, UPCs: 30034-30012, 30034-30400, 30034-30363; Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1592-2012·2012-08-15

    River Ranch Shredded Green Cabbage Recalled for Listeria Contamination

    River Ranch Fresh Foods LLC is recalling Shredded Green Cabbage with Color due to Listeria monocytogenes contamination found in FDA samples.

    Product
    River Ranch brand Shred Grn Cabbage w/Color, 4 x 5lb bag, UPC: n/a; Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product is processed and packaged by River Ranch…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1575-2012·2012-08-15

    River Ranch Recalls Farmers Market Cole Slaw Due to Listeria Risk

    River Ranch Fresh Foods is recalling The Farmers Market brand Cole Slaw because FDA samples tested positive for Listeria monocytogenes.

    Product
    The Farmers Market brand Cole Slaw, 16 oz bag, UPC: 30034-30013; Product is a salad item; bagged in clear polyethylene film (foodservice) and polypropylene/polyethylene (retail). Refrigerate and consume within Best By date. Product is processed and packaged by River Ranch Fresh…
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-2171-2012·2012-08-15

    Abbott i-Stat CK-MP Cartridges Recalled for Atmospheric Pressure Interference

    Abbott Point of Care Inc. is recalling i-Stat CK-MP cartridges because atmospheric pressure can cause suppressed test results, potentially affecting the diagnosis of myocardial infarction.

    Product
    i-Stat CK-MP cartridges Abbott Point of Care Inc. The i-Stat CKMB test is an in vitro diagnostic test for the quantitative measurement of creatinine kinase MB mass in whole blood or plasma samples. CK-MB measurements can be used as an aid in the diagnosis and treatment of…
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2157-2012·2012-08-15

    Abbott i-STAT PT/INR Cartridges Recalled for Incorrectly Elevated Results

    Abbott Point of Care Inc. is recalling i-STAT PT/INR cartridges because they may display incorrectly elevated results, potentially affecting monitoring of patients on anticoagulation therapy.

    Product
    I-STAT PT/INR cartridge Abbott Point of Care Inc. Abbott Park, IL 60064 USA This cartridge is useful for monitoring patients receiving oral anticoagulation therapy such as Coumadin or warfarin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2166-2012·2012-08-15

    Smith & Nephew TWINFIX Ultra Ti Anchor Recall for Breakage Risk

    Smith & Nephew is recalling 4,661 units of TWINFIX Ultra Ti Anchors because the distal part may break during insertion into bone.

    Product
    Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white, COBRAID-blue), sterile Part Number: 72202895 Product Usage: intended for use for the reattachment of soft tissue to bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2151-2012·2012-08-15

    ConMed Linvatec Recalls PopLok Bone Punch Due to Incorrect Shaft Diameter

    ConMed Linvatec recalled one lot of PopLok bone punches because the metal shaft diameter was 4.5mm instead of the intended 3.5mm.

    Product
    PopLok Punch labeled in part: "PKL-35M***3.5mm***QTY 1***PopLok Punch***ConMed Linvatec Biomaterials, Ltd. Hermiankatu 6-8L 33720 Tampere, FINLAND***Rx Only***ConMed Linvatec 11311 Concept Blvd Largo, FL 33773-4908 USA***Made in USA***" Intended Use: Bone Punch.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2178-2012·2012-08-15

    Terumo Advanced Perfusion System 1 recalled for module malfunctions

    Terumo is recalling 649 Advanced Perfusion System 1 units worldwide due to faulty components in the Occluder and Air Bubble Detection modules.

    Product
    System 1 base 220/240V The Terumo Advanced Perfusion System 1 is indicated for use in extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures only when used by a qualified perfusionist who is experienced in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V398000·2012-08-14

    Nissan Recalls 2013 Infiniti JX35 for Fuel Gauge Inaccuracy

    Nissan is recalling 7,842 2013 Infiniti JX35 vehicles because a misrouted fuel tube may cause the fuel gauge to read higher than the actual level, increasing the risk of stalling.

    Product
    INFINITI — INFINITI JX35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12245·2012-08-14

    Toysmith Recalls Animal Snap Bracelets Due to Laceration Hazard

    Toysmith is recalling Animal Snap Bracelets because the metal snap band can wear through the fabric, exposing sharp edges that pose a laceration hazard.

    Product
    Animal Snap Bracelet
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·12V397000·2012-08-14

    Suzuki Recalls Forenza and Reno Vehicles for Headlamp Wiring Defect

    Suzuki is recalling 2004-2006 Forenza and 2005-2006 Reno vehicles because poor wire contact can melt headlamp connections, causing loss of lights and increased crash risk.

    Product
    SUZUKI — SUZUKI FORENZA, RENO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12V404000·2012-08-14

    Turtle Top Transit Buses Recalled for Wheelchair Lift Latch Defect

    Turtle Top is recalling 2006-2010 transit buses with specific wheelchair lifts because roll stop latches may bend, posing a fall risk to occupants.

    Product
    TURTLE TOP — TURTLE TOP TERRA TRANSPORT, FORD ODYSSEY, FORD VAN TERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·12E028000·2012-08-09

    Mercedes-Benz Recalls Accessory Floor Mats for ML-Class Vehicles

    Mercedes-Benz is recalling accessory all-season floor mats for 2012-2013 ML-Class vehicles because they may trap the gas pedal, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ ML550, ML350, AMG ML63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2128-2012·2012-08-08

    ICU Medical Recalls High Pressure Stopcocks Due to Molding Defect

    ICU Medical is recalling 4,625 High Pressure Stopcocks because a molding defect may cause side ports to become totally occluded.

    Product
    High Pressure Stopcock (3-Way, Luer Lock, Off). Product Usage: For IV.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2125-2012·2012-08-08

    GE OEC Medical Systems Recalls OEC 9800 Plus Digital Imaging Systems

    GE OEC Medical Systems is recalling OEC 9800 Plus Digital imaging systems due to a hard disk drive issue. The recall covers 82 units distributed worldwide.

    Product
    OEC 9800 Plus Digital; MDL number A349855. Product Usage: Is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clinical applications may include cholangiography, endoscopic, urologic, orthopedic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1823-2012·2012-08-08

    Spillson's Greek Pita Sandwich Recalled for Undeclared Wheat

    Spillson's, Ltd. is recalling Greek Pita Sandwiches due to undeclared wheat in the flour ingredient. People with wheat allergies or sensitivities are at risk of serious reactions.

    Product
    Spillson's Ltd.Greek Pita Sandwich Nt. Wt. 7oz.
    Category
    Food
    Distribution
    1 state