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.

32851–32875 of 50502

  • HighFDA (Food)·F-1667-2017·2017-03-29

    Carriage House Creations Recalls Hot Barbecue Sauce for Undeclared Allergens

    Carriage House Creations is recalling Hot Barbecue Sauce due to undeclared peanuts and soy. The recall was triggered by a notification regarding a Worcestershire sauce ingredient.

    Product
    Hot Barbecue Sauce; Net wt. 16 ounces; Manufactured by Carriage House Creations, 544 Gordon Alley, Reynoldsville, PA 15851;
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1514-2017·2017-03-29

    Medtronic Poly Component Trial Knee Implants Recalled for Cracked Dovetails

    Medtronic is recalling 72 Poly Component Trial knee implants because their dovetails were observed as cracked or broken.

    Product
    Poly Component Trial, UCCS, packaged in the following sizes and configurations: a) Poly Comp Trial - UCCS 3x10, REF 90-SRK-170310 b) Poly Comp Trial - UCCS 3x12, REF 90-SRK-170312 c) Poly Comp Trial - UCCS 3x14, REF 90-SRK-170314 d) Poly Comp Trial - UCCS 4x10, REF…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1711-2017·2017-03-29

    Country Fresh Tuscan Style Portabella Mushrooms Recalled for Listeria Risk

    Country Fresh Inc. is recalling Tuscan Style Portabella Mushrooms due to possible contamination with Listeria monocytogenes. The product was distributed across ten southeastern and southern states.

    Product
    Country Fresh Creations Tuscan Style Portabella Mushrooms Net Wt. 8oz (227g) Distributed by Country Fresh, LLC., Houston, TX 77090 UPC: 074641072115
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-1543-2017·2017-03-29

    Medtronic Recalls Endurant Bifurcated Stent Grafts Due to Fabric Permeability

    Medtronic is voluntarily recalling specific Endurant and Endurant II bifurcated stent graft systems because fabric permeability variations may be associated with endoleaks during initial implant procedures.

    Product
    Endurant / Endurant II 23mm and 25mm Bifurcated Stent Graft Systems Model Numbers: ETBF2516C145E ETBF2516C166E ETBF2316C145E ETBF2313C145E ETBF2513C166E ETBF2313C166E ETBF2316C166E ETBF2313C124E ETBF2513C145E ETBF2516C124E ETBF2316C124E ETBF2513C124E.…
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-1641-2017·2017-03-29

    Manzana Recalls Trader Joe's Apple Sauce Due to Glass Fragments

    Manzana Products Co. is recalling Trader Joe's All Natural Unsweetened Apple Sauce after finding small pieces of glass in the product.

    Product
    Trader Joe's All Natural Unsweetened Apple Sauce; 24 oz. glass jar. Best Before date stamped on top of lid. UPC: 00014359 Distributed by Trader Joe's, Monrovia, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1485-2017·2017-03-29

    PureWick External Catheter Recalled for Latex Labeling Errors

    Purewick Corporation is recalling 176,863 units of the PureWick External Catheter for Women because the labeling failed to disclose the presence of dry natural rubber and incorrectly stated the product was latex-free.

    Product
    PureWick External Catheter for Women-Wick Product Usage: A flexible, contoured external catheter (a Wick) is positioned between the labia and gluteus muscles. The function of the Wick is to draw urine away from the body through the Wick to a storage container away from the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1716-2017·2017-03-29

    Chapis Spice & Tea Recalls Seasoned Bread Crumbs for Undeclared Allergens

    Chapis Spice & Tea is recalling Pan Molido Sazonado Seasoned Bread Crumbs due to undeclared allergens including wheat, milk, eggs, tree nuts, and soybean.

    Product
    Pan Molido Sazonado Seasoned Bread Crumbs, Net Wt. 6oz and 12oz
    Category
    Food
    Distribution
    0 states
  • HighCPSC·17117·2017-03-28

    Look Cycle Recalls Road Bikes and Aerostems Due to Fall Hazards

    Look Cycle is recalling about 800 road bikes and Aerostems because a stainless steel clamp can corrode and break, posing a fall and crash hazard.

    Product
    Look Cycle road bikes and Aerostems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17736·2017-03-28

    SolarWorld Recalls Solar Panel Connectors Due to Electrical Shock Hazard

    SolarWorld is recalling about 97,000 solar panel connectors sold in the U.S. because microscopic cracks can allow moisture to leak in, posing an electrical shock hazard.

    Product
    Connectors sold with solar panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V210000·2017-03-27

    Ford Recalls 2013-2014 Vehicles Due to Door Latch Defect

    Ford is recalling 2013-2014 Lincoln MKZ, Ford Fusion, and 2014 Ford Fiesta vehicles because door latches may break, leaving doors unsecured.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, FIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V206000·2017-03-27

    Keystone Recalls 2017 Cougar Trailers Due to Fire Risk

    Keystone is recalling 2017 Cougar recreational trailers because a manual-resetting circuit breaker near propane storage may spark and cause a fire.

    Product
    KEYSTONE — KEYSTONE COUGAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17113·2017-03-23

    Little Giant Ladders Recalled Due to Locking Pin Failure Hazard

    Wing Enterprises is recalling Little Giant ladders because locking pins can fail, posing a fall hazard. No injuries have been reported.

    Product
    Little Giant multipurpose ladders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V202000·2017-03-23

    Blue Bird Recalls 2016 School Buses Due to Seat Belt Defect

    Blue Bird is recalling 2016 Vision and All American school buses because loose or missing nuts may allow shoulder belt D-rings to detach in a crash.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1449-2017·2017-03-22

    LeMaitre Vascular Catheter Recalled for Missing Latex Warning Label

    LeMaitre Vascular is recalling Reddick Cholangiogram Stiffer Catheters because the latex warning symbol was missing from the packaging.

    Product
    LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (paper IFU) REF# 2401-51
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1456-2017·2017-03-22

    Maquet Recalls VASOVIEW HEMOPRO VH-3500 Endoscopic Vessel Harvesting System

    Maquet Cardiovascular is recalling 4,283 VASOVIEW HEMOPRO VH-3500 units due to reports of intermittent or no power.

    Product
    VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage: The VASOVIEW HEMOPRO VH-3500 is designed for use in conjunction with the 7-mm Endoscope and is intended for specific use with the VASOVIEW HEMOPRO Power Supply.
    Category
    Medical Device
    Distribution
    Distributed nationwide