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.

34126–34150 of 50502

  • HighFDA (Devices)·Z-0086-2017·2016-11-09

    Epimed 15 g R.K. Epidural Needle Recall for Catheter Coating Risk

    Epimed International is recalling 576 units of 15 g R.K. Epidural Needles because they may skive a catheter's outer coating, posing a risk of retained catheter fragments.

    Product
    15 g R.K. Epidural Needle (TW), Catalog #/REF #100-1415 Intended for the epidural placement, directly or through an epidural catheter, of anesthetic agents to elicit regional anesthesia
    Category
    Medical Device
    Distribution
    6 states
  • HighCPSC·17709·2016-11-08

    Trane Recalls Furnaces Due to Electrical Shock Hazard

    Trane is recalling about 17,700 furnaces because a loose ground wire creates a shock hazard if an electrical component fails.

    Product
    Furnaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V813000·2016-11-08

    Chrysler Recalls 2016 Dodge Dart for Windshield Wiper Circuit Failure

    Chrysler is recalling 53,155 2016 Dodge Dart vehicles because a faulty washer pump can cause the wiper circuit to fail, reducing visibility and increasing crash risk.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V805000·2016-11-04

    Terex Recalls 2009-2014 TC and TCX Trucks for Wiring Defect

    Terex is recalling 2009-2014 TC and TCX hybrid electric trucks because improper wiring may cause the aerial boom to move unintentionally, increasing the risk of injury.

    Product
    TEREX — TEREX TC, TCX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V801000·2016-11-03

    E-One Recalls 2014-2016 Fire Trucks Due to Hydraulic Leak Risk

    E-One is recalling 2014-2016 Typhoon, Quest, and Cyclone fire trucks equipped with aerial ladders because a filter design change may cause hydraulic fluid leaks.

    Product
    E-ONE — E-ONE CYCLONE, QUEST, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17027·2016-11-03

    KTM and Husqvarna Recall Off-Road Motorcycles Due to Brake Malfunction

    KTM North America is recalling about 1,200 model year 2017 KTM and Husqvarna off-road motorcycles because the front brake master cylinder can malfunction, posing a crash hazard.

    Product
    Closed-course/competition off-road motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0316-2017·2016-11-02

    Aesculap Safil Suture Recall Due to Needle Detachment Risk

    Aesculap is recalling 180 units of Safil QUI + UNDY 5/0 sutures because the needle may detach from the thread during surgery.

    Product
    Safil QUI + UNDY 5/0 (1) 45CM DSMP13 Suture
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0314-2017·2016-11-02

    BBI Solutions Recalls SimpliRED D-Dimer Assay Kits Due to Performance Issues

    BBI Solutions is recalling SimpliRED D-Dimer assay kits because stability testing showed reduced sensitivity, which may cause false negative results and affect clinical decisions.

    Product
    SimpliRED D-Dimer, Product Code DSRK4 The SimpliRED D-dimer assay is a rapid, qualitative test for the detection of cross-linked fibrin degradation products containing the cross-linked D-diner site in human whole blood
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·16V799000·2016-11-02

    Jeep Cherokee Recall for Driver Knee Air Bag Weld Defect

    Chrysler is recalling 2017 Jeep Cherokee vehicles because improper welds may prevent the driver's knee air bag from inflating properly.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0304-2017·2016-11-02

    Nova Medical Recalls Journey Rolling Walkers Due to Loose Screws

    Nova Medical is recalling 1,380 Journey Rolling Walkers because screws holding the side supports can loosen and fall out.

    Product
    4205 Journey Rolling Walker Product Usage: used to assist people in walking
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0179-2017·2016-11-02

    Porfirio's Ricotta Gnocchi Recalled for Undeclared Wheat and Milk

    Porfirio's Homeade Ricotta Gnocchi is being recalled because it may contain undeclared wheat and milk allergens.

    Product
    Porfirio's Homeade Ricotta Gnocchi Net Wt. 16 oz (1 LB.) 453 g Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ 08611 UPC 016105000319
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0305-2017·2016-11-02

    Hospira Symbiq Infuser Recall for Potential White Screen Error

    Hospira is recalling Symbiq One Channel Infusers because a white screen during KVO titration may allow premature programming, potentially causing therapy delays and significant injury.

    Product
    Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0114-2017·2016-11-02

    Sequent Medical Recalls VIA 27 Microcatheter Due to Re-sheathing Defect

    Sequent Medical is recalling 618 units of the VIA 27 Microcatheter because the device may not adequately re-sheath interventional devices as designed.

    Product
    VIA 27 Microcatheter, Part No. FG27-154-01, Model No. VIA-27-154-01 The VIA 27 is intended for the introduction of non-liquid interventional devices (such as stents/flow diverters) and infusion of diagnostic (such as contrast media) or therapeutic agents into the neuro…
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-0278-2017·2016-11-02

    Nestle Drumstick Ice Cream Recalled for Possible Listeria Contamination

    Nestle USA is voluntarily recalling specific Drumstick ice cream packs due to possible Listeria monocytogenes contamination from equipment contact surfaces.

    Product
    Nestle Drumstick Vanilla pack- 24x4.6fl oz US UPC# 72554-00160 Best Before Date: Between June 16 - June 19, 2017
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0184-2017·2016-11-02

    Porfirio's Jumbo Cheese Ravioli Recalled for Undeclared Wheat and Milk

    Porfirio's 12 Jumbo Cheese Ravioli is being recalled because it may contain undeclared wheat and milk allergens.

    Product
    Porfirio's 12 Jumbo Cheese Ravioli Net Wt. 14 oz. Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ 08611
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0103-2017·2016-11-02

    Roche VS II Aliquoter System recalled due to sharp edge injury risk

    Roche is recalling VS II Aliquoter System calculator modules because a sharp edge on the sample rack tray caused four reported injuries.

    Product
    VS II Aliquoter System calculator/data processing module, for clinical use Product Usage: Elecysy 411 analyzer is a fully automated, random access, computer controlled analytical systems for quantitative and qualitative determinations of analytes in body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0279-2017·2016-11-02

    Del Monte Recalls Mislabeled Lite Sliced Peaches Cans

    Del Monte is recalling cans of Lite Sliced Peaches that were mislabeled and actually contained Fruit Cocktail in Heavy Syrup. The product contains carmine, an ingredient that requires specific labeling.

    Product
    DM Light Slices Yellow Cling Peaches -15 oz (425g) 300 x 407
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0315-2017·2016-11-02

    Intuitive Surgical Recalls da Vinci Xi Systems Due to Software Anomaly

    Intuitive Surgical is recalling 677 da Vinci Xi Surgical Systems due to a software anomaly that may cause unexpected movement.

    Product
    da Vinci¿ Xi" Surgical System, model number IS4000, A70_P5x with P5 Software; General and Plastic Surgery: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical…
    Category
    Medical Device
    Distribution
    1 state