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.

34151–34175 of 50502

  • HighFDA (Devices)·Z-0306-2017·2016-11-02

    Hospira Symbiq Infuser Recall for Potential White Screen Error

    Hospira is recalling Symbiq Two Channel Infusers because a white screen error during KVO titration could delay therapy and cause significant injury.

    Product
    Symbiq Two 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-0301-2017·2016-11-02

    Lumenis Recalls FemTouch Delivery System Due to Ineffective Cleaning Instructions

    Lumenis Limited is recalling 69 units of the FemTouch delivery system because the provided cleaning instructions may be ineffective for fully assembled devices, posing a risk of cross-contamination.

    Product
    FemTouch delivery system includes the FemTouch Kit (AC-1007415) and FemTouch" Tip (SPSA-20002590) Provide fractional treatments in gynecology.
    Category
    Medical Device
    Distribution
    0 states
  • HighCPSC·17026·2016-11-02

    Pier 1 Imports Recalls Glass Knobs Due to Laceration Hazard

    Pier 1 Imports is recalling approximately 140,000 glass knobs sold in the U.S. because they can break during use, posing a risk of laceration.

    Product
    Glass knobs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0357-2017·2016-11-02

    Wilton Blue Airbrush Color Recalled Due to Mold and Bacteria Contamination

    Wilton Brands is recalling 16,188 bottles of Blue Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.

    Product
    Wilton Blue Airbrush Color, Net Wt 0.64 FL OZ (19 mL)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0277-2017·2016-11-02

    Nestle Drumstick Ice Cream Recalled for Possible Listeria Contamination

    Nestle USA is voluntarily recalling specific Drumstick Club and Vanilla packs due to possible Listeria monocytogenes contamination from equipment contact surfaces.

    Product
    Nestle Drumstick Club variety - 16x4.6floz US UPC# 72554-11096 Best Before Date: Between June 2 - June 15, 2017
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-0297-2017·2016-11-02

    AccessClosure Recalls PAXWIRE Occlusion Balloon System Due to Removal Risk

    AccessClosure, Inc. is voluntarily recalling the PAXWIRE Occlusion Balloon System because the device may be removed without a vascular sheath in place.

    Product
    The PAXWIRE Occlusion Balloon System consists of an occlusion catheter, inflation handle and syringes. It is designed for use in the iliofemoral artery to provide temporary occlusion as well as a path for dilator and/or sheath introduction, removal or repositioning during…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0182-2017·2016-11-02

    Porfirio's 6 Cheese Manicotti Recalled for Undeclared Wheat and Milk

    Porfirio's 6 Cheese Manicotti is being recalled because it may contain undeclared wheat and milk, posing a risk to individuals with allergies.

    Product
    Porfirio's 6 Cheese Manicotti Net Wt. 22 oz. Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ 08611
    Category
    Food
    Distribution
    2 states
  • HighFDA (Drugs)·D-0113-2017·2016-11-02

    Persantine Tablets Recalled Due to Presence of Foreign 50 mg Tablets

    Boehringer Ingelheim is recalling 2,562 bottles of 75 mg Persantine tablets because 50 mg tablets were found inside the bottles.

    Product
    Persantine (dipyridamole USP) tablets, 75 mg, 100-count bottles, Rx only, Dist. by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877, NDC 0597-0019-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0186-2017·2016-11-02

    Porfirio's Cheese and Spinach Manicotti Recalled for Undeclared Allergens

    Porfirio's Italian Foods is recalling Cheese & Spinach Manicotti due to undeclared wheat and milk allergens. The product was distributed in New Jersey and Pennsylvania.

    Product
    Porfirio's Cheese & Spinach Manicotti Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ 08611
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0181-2017·2016-11-02

    Porfirio's Spinach Ravioli Recalled for Undeclared Wheat and Milk

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

    Product
    Porfirio's 12 Jumbo Spinach Ravioli Net Wt. 14 oz. (1 LB.) 453 g Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ 08611
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0185-2017·2016-11-02

    Porfirio's Egg Fettucine Recalled for Undeclared Wheat and Milk

    Porfirio's Italian Food, Inc. is recalling 1,400 lbs of Egg Fettucine due to undeclared wheat and milk allergens. The product was distributed in New Jersey and Pennsylvania.

    Product
    Porfirio's Egg Fettucine Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ 08611
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0183-2017·2016-11-02

    Porfirio's Stuffed Shells Recalled for Undeclared Wheat and Milk

    Porfirio's 12 Jumbo Stuffed Shells are being recalled because they may contain undeclared wheat and milk allergens.

    Product
    Porfirio's 12 Jumbo Stuffed Shells Net Wt. 24 oz. Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ 08611
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-0178-2017·2016-11-02

    Porfirio's Potato Gnocchi Recalled for Undeclared Wheat and Milk

    Porfirio's Potato Gnocchi is being recalled because it may contain undeclared wheat and milk, posing a risk to consumers with allergies.

    Product
    Porfirio's Potato 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 (Food)·F-0180-2017·2016-11-02

    Porfirio's Ricotta Cavatelli Recalled for Undeclared Wheat and Milk

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

    Product
    Porfirio's Homeade Ricotta Cavatelli Net Wt. 1Lb Manufactured by Porfirio's Italian Food, Inc. 320 Anderson Street, Trenton NJ
    Category
    Food
    Distribution
    2 states
  • HighCPSC·17025·2016-11-02

    Trek Recalls Farley Bicycles Due to Fork Separation Fall Hazard

    Trek Bicycle Corp. is recalling 2014 and 2015 Farley bicycles and framesets because the fork can separate from the steer tube, posing a fall hazard to the rider.

    Product
    Trek Farley bicycles and framesets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0114-2017·2016-11-02

    Boehringer Ingelheim Recalls Dipyridamole Tablets Due to Foreign Tablet Presence

    Boehringer Ingelheim is recalling 6,400 bottles of 75 mg Dipyridamole tablets because 50 mg Persantine tablets were found inside the bottles.

    Product
    DIPYRIDAMOLE Tablets USP, 75 mg, 100-count bottle, Rx only, Dist. by: Roxane Laboratories, Inc., Columbus, Ohio 43216, NDC 0054-0436-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·17023·2016-11-01

    Kikkerland Teapots with Bamboo Stands Recalled for Fire Hazard

    Kikkerland Design is recalling teapots with bamboo stands because the stands can catch fire. No injuries have been reported.

    Product
    Kikkerland and Cost Plus World Market brand teapots with bamboo stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V792000·2016-10-31

    Mitsubishi Recalls Outlander Sport Vehicles for Wiper Motor Corrosion Risk

    Mitsubishi is recalling 2011-2015 Outlander Sport vehicles because water leaks can corrode the wiper motor, potentially causing loss of visibility and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V791000·2016-10-31

    Mitsubishi Recalls Outlander Vehicles for Wiper Link Corrosion Risk

    Mitsubishi is recalling 2007-2013 Outlander vehicles because water intrusion can corrode the wiper link, potentially causing the wipers to stop working and reducing visibility.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E081000·2016-10-28

    Vega Motorcycle Helmets Recalled for Failing Federal Safety Standards

    Vega Helmet Corporation is recalling specific XTA and XTA Touring half helmets because they may not adequately protect the wearer's head in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V787000·2016-10-28

    Forest River Recalls 2017 Salem and Wildwood Trailers for Labeling Errors

    Forest River is recalling 92 model year 2017 Salem and Wildwood recreational trailers because the Federal Placard Label and VIN incorrectly state the vehicles have two axles instead of one.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide