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.

44476–44500 of 50511

  • HighFDA (Devices)·Z-0199-2013·2012-11-28

    GE Healthcare Recalls Mobile Radiographic Units Due to Firmware Issue

    GE Healthcare is recalling specific mobile radiographic units due to a firmware issue affecting technique accuracy as mandated by federal regulations.

    Product
    GE Healthcare Optima 200amx Mobile general purpose radiographic imaging of the human head and body.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0412-2013·2012-11-28

    Spine Frontier Inspan Compressors Recalled for Potential Weld Breakage

    SpineFrontier, Inc. is recalling 17 Inspan compressors because they may break at the weld, causing a loss of compression during use.

    Product
    Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors provide pressure to drive spikes of Inspan implants into the spinous process bone, resulting in fixation of the implant.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13048·2012-11-27

    Toro Z Master Riding Mowers Recalled Due to Fire Hazard

    Toro is recalling 2012 Z Master Commercial 2000 Series riding mowers because a worn traction drive belt can puncture the fuel tank, causing a leak and fire hazard.

    Product
    Toro® Z Master® Riding Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13049·2012-11-27

    Step2 Recalls X-Rider Car Due to Fall Hazard

    Step2 is recalling about 15,500 X-Rider Car toys because children can fall over the handlebar. The company is offering free replacements.

    Product
    Children's Riding Toy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·12V542000·2012-11-23

    Toyota Recalls 2001-2004 Tacoma Trucks for Spare Tire Carrier Defect

    Toyota is recalling 2001-2004 Tacoma trucks in cold climate states because the spare tire carrier lift plate may corrode and break, causing the tire to detach.

    Product
    TOYOTA — TOYOTA TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0287-2013·2012-11-21

    Dako PT Link Waterbath Recalled for Electrical Shock Hazard

    Dako North America Inc. is recalling 136 PT Link Waterbath units due to a potential electrical shock hazard if the heater pad becomes wet.

    Product
    PT Link Waterbath, Model#PT100. Lab Vision PT Module Plus provides an automated standarized alternative to labor intensive and time consuming dewaxing and epitote retrieval procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0280-2013·2012-11-21

    Terumo Recalls Sarns Modular Perfusion System 8000 Due to Monitor Malfunctions

    Terumo CVS is recalling 274 Sarns Modular Perfusion System 8000 units due to reported malfunctions in arterial and cardioplegia monitors, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 4 pump, 115V 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, when…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13707·2012-11-21

    Hunter Douglas Recalls Custom Cellular and Pleated Window Coverings for Strangulation Hazard

    Hunter Douglas is recalling about 4,400 custom cellular and pleated window coverings because a knot in the cord stop may prevent it from breaking away, creating a strangulation risk for children.

    Product
    Standard cordlock top-down/bottom-up Duette and Applause honeycomb shades; standard cordlock top-down/bottom-up Hunter Douglas pleated shades; Hunter Douglas Brilliance Privacy View pleated shades and standard cordlock Duette and Applause Duolite shades
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0279-2013·2012-11-21

    Terumo HX2 Temperature Management System Recalled for Board Defect

    Terumo is recalling 15 HX2 Temperature Management Systems because AC Control boards were manufactured with incorrect flux, which may cause premature failure.

    Product
    Tested AC Control BD, 120V, X2 The Terumo HX2 Temperature Management System is a selfcontained, dual channel system for supplying temperature controlled water to heat exchangers used in an extracorporeal circuit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0680-2013·2012-11-21

    Taco Loco Salmon Wrap Recalled for Undeclared Soy Allergen

    Taco Loco Products Inc is recalling Salmon Wraps because the product contains soy oil and soy, which were not declared on the label.

    Product
    Salmon Wrap. Two wraps per package. Net Wt 8 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0690-2013·2012-11-21

    Mazzio's Marinara Sauce Recalled for Undeclared Milk Allergen

    Paradise Tomato Kitchens Inc is recalling Mazzio's Marinara Sauce because the ingredient statement fails to declare milk as the source of butter.

    Product
    Mazzio's Marinara Sauce, 6.65-lb pouch, 6 pouches per case Pouches are packed in cardboard box for shipment
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0698-2013·2012-11-21

    Zatarain's Chicken and Cheddar Broccoli Mix Recalled for Undeclared Wheat

    McCormick & Company is recalling Zatarain's Chicken/Cheddar Broccoli Mix because the product contains wheat but the label does not declare it.

    Product
    Zatarain's Chicken/Cheddar Brocolli Mix, Item Number: 900108337, a combination pack containing, 6.3 oz boxes of New Orleans Style Chicken Flavor Rice Mix and Cheddar Broccolli Mix.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0657-2013·2012-11-21

    American Vines Black Soft Licorice Twists Recalled for Lead Contamination

    American Licorice Co is recalling specific lots of American Vines Black Soft Licorice Twists due to elevated lead levels found during internal sampling.

    Product
    American Vines band Natural Vines Black Soft Licorice Twists; All Natural Ingredients, 8 oz (226g), No Preservatives, Product is processed and packaged by American Licorice Company, Union City, CA; Displays and Pallets info: ----6 ct. Case, Item: #8483, Case UPC…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0296-2013·2012-11-21

    Zimmer Recalls ATS 3000 Tourniquets Due to Counterfeit Chip Failures

    Zimmer is voluntarily removing 204 ATS 3000 Automatic Tourniquet Systems worldwide after complaints of failures caused by counterfeit chips.

    Product
    ATS 3000 Automatic Tourniquet System w/HOSES AND LOP SENSOR Intended to be used by qualified medical professionals to temporarily occlude blood flow in a patient's extremities during surgical procedures on those extremities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0286-2013·2012-11-21

    Stryker Recalls Peri-Acetabular Prosthesis Femoral Extension Components

    Stryker Howmedica Osteonics is recalling 301 units of Peri-Acetabular Prosthesis V40 Femoral Extension Components due to insufficient taper torsional strength when used with forged CoCr stems.

    Product
    Special Orthopaedic Solution Peri-Acetabular Prosthesis V40 Femoral Extension Component Product Usage: The PAR extension piece is a component of the PAR assembly. The Peri-Acetabular Reconstruction (PAR) endoprosthesis was developed to meet the unique needs of patients…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0288-2013·2012-11-21

    Trivascular Recalls Fill Polymer Kits Due to Potential Stopcock Leaks

    Trivascular is recalling 41 units of Fill Polymer Kits in European distributor inventory due to potential stopcock cracks that may cause leaks.

    Product
    TriVascular brand Fill Polymer Kit, Endovascular Graft, Aneurysm Treatment System, European Model Number: TVFP14-B, (in European distributor inventory only); PRODUCT Usage: The TriVascular Ovation Abdominal Stent Graft System is indicated in subjects diagnosed with an…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0294-2013·2012-11-21

    MOOG Recalls EnteraLite Infinity Enteral Feeding Pumps Due to Voltage Defect

    MOOG Medical Devices Group is voluntarily recalling specific EnteraLite Infinity enteral feeding pumps because a PCB defect may cause the device to shut down.

    Product
    EnteraLite Infinity Enteral Feeding Pump identified with the following list numbers: INFKIT2 and INFORNG. The device is used with disposable PVC administration tubing sets to provide a means for the volumetric delivery of fluids used in enteral applications. The EnteraLite…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0658-2013·2012-11-21

    Aunt Marie's Bakery Cookie Dough Recalled for Foreign Object

    RDK Corp is recalling Aunt Marie's Bakery Gourmet Cookie Dough due to a foreign object hazard. The product was distributed to fund-raising organizations in Arizona, Illinois, and Wisconsin.

    Product
    Aunt Marie's Bakery Gourmet Cookie Dough, Chocolate Chunk, packaged in 3-lb. plastic tubs. Distributed by Racine Danish Kringles, Racine, WI.
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0681-2013·2012-11-21

    Zatarain's Beef Flavor Rice Mix Recalled for Undeclared Wheat

    McCormick & Company is recalling Zatarain's New Orleans Style Beef Flavor Rice Mix because the product contains wheat but the label does not declare it.

    Product
    Zatarain's New Orleans Style Beef Flavor Rice Mix, packaged in 6.8 oz boxes, 12 boxes per carton, Box UPC: 7142901001
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0281-2013·2012-11-21

    Terumo Sarns Modular Perfusion System 8000 Recalled for Monitor Malfunctions

    Terumo CVS is recalling Sarns Modular Perfusion System 8000 units due to reported malfunctions in arterial and cardioplegia monitors, including power issues and inaccurate pressure alarms.

    Product
    Perfusion System 8000, base 5 pump, 115V 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, when…
    Category
    Medical Device
    Distribution
    Distributed nationwide