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.

40726–40750 of 50511

  • HighNHTSA·14V494000·2014-08-08

    Vanair Recalls Ford Super Duty Trucks Due to Fire Risk

    Vanair is recalling 2009-2013 Ford F-350, F-450, and F-550 Super Duty trucks modified with specific air compressor systems because oil leaks may cause a fire.

    Product
    FORD — FORD F-450 SUPER DUTY, F-550 SUPER DUTY, F-350 SUPER DUTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14252·2014-08-07

    Lea Industries Recalls Lighted Night Stands Due to Burn Hazard

    Lea Industries is recalling about 520 lighted night stands sold in the U.S. and Canada because the under-lighting can overheat and scorch carpets, posing a burn hazard.

    Product
    Lea lighted night stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14742·2014-08-07

    L.L. Bean Recalls Children's Sweaters Due to Choking Hazard

    L.L. Bean is recalling specific children's sweaters because a spare button can detach and pose a choking hazard. No injuries have been reported.

    Product
    Fisherman's and Open Stitch Children's Sweaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2227-2014·2014-08-06

    Malt-O-Meal Frosted Flakes Bowls Recalled for Undeclared Honey and Oats

    mom Brands is recalling Malt-O-Meal Frosted Flakes foodservice bowls because they may contain undeclared honey and oats.

    Product
    Malt-O-Meal Frosted Flakes, item number 00955, UPC 42400-00955. Net Wt. 2.00oz (56g)
    Category
    Food
    Distribution
    5 states
  • HighFDA (Drugs)·D-1496-2014·2014-08-06

    Fagron Recalls Phytobase Cream Lots Due to Mold Contamination

    Fagron is recalling six lots of Phytobase Cream, a prescription compounding vehicle, due to the presence of mold.

    Product
    Fagron, Phytobase Cream, 500 g, Article number: 802156. RX only, For prescription compounding Natural self-emulsifying oil-in water vehicle for oil-solvents ingredients. Contains Phytosomes (Plant Oil Bodies), Manufactured by Fagron, Inc. 2400 Pilot Knob Rd, St Paul, MN 55120…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·14V481000·2014-08-06

    Fiat 500L Recall: Driver Knee Airbag May Deploy Improperly

    Chrysler is recalling 2014-2015 Fiat 500L vehicles because the driver's knee airbag may not deploy correctly, increasing injury risk in a crash.

    Product
    FIAT — FIAT 500L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2122-2014·2014-08-06

    Stryker InTouch Critical Care Bed Recall Due to Caster Failure

    Stryker is recalling InTouch Critical Care Beds because casters may break and fall off, potentially affecting brake functions.

    Product
    InTouch Critical Care Bed, Stryker Medical. Model Numbers 2130, 2131, 2140, 2141, 2151, 2152, 2155, and 2156.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V485000·2014-08-06

    Newmar Recalls 2014 Dutch Star Motorhomes for Headlight Wiring Defect

    Newmar is recalling 2014 Dutch Star motorhomes because an incorrectly wired headlight harness may cause both headlights and fog lights to fail, increasing crash risk.

    Product
    NEWMAR — NEWMAR DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1498-2014·2014-08-06

    Fagron Recalls Pentravan Plus Base Due to Mold Contamination

    Fagron is recalling specific lots of Pentravan Plus Base, a prescription compounding ingredient, because of mold contamination.

    Product
    Fagron, Pentravan Plus Base 2.5 Kg, Article number: 804749. RX only, For prescription compounding, Oil-in-water emulsion base alternative to PLO gel, Added emulsifier ad viscosity-enhancing agent for use with high concentrations of active ingredients.Pre served and…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2236-2014·2014-08-06

    Plaze Bak-klene Bakery Spray Recalled for Undeclared Wheat

    Plaze Inc is recalling Professional Bak-klene All Purpose No-Stick Bakery Spray because it contains undeclared wheat.

    Product
    Professional Bak-klene All Purpose No-Stick Bakery Spray, packaged in 14-oz. aerosol cans.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2131-2014·2014-08-06

    Zimmer Recalls 28 Distal Radial Volar Plates Due to Screw Locking Failure

    Zimmer, Inc. is recalling 28 units of the Distal Radial Volar Plate Lateral Column because a defect prevented screws from locking, causing them to pull through the plate.

    Product
    Zimmer Periarticular Locking Plate System Distal Radial Volar Plate Lateral Column (1st generation stainless steel only). Orthopedic fixation plate. For temporary internal fixation and stabilization of osteotomies and fractures.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2118-2014·2014-08-06

    Medtronic Nexdrive Micropositioning Drive Recalled for Potential Misalignment

    Medtronic is recalling Nexdrive Micropositioning Drives because a scale misalignment could cause microelectrodes to be inserted at incorrect depths during surgery.

    Product
    Medtronic Nexdrive Micropositioning Drive. Models Ml-1000 and Ml-2000. For use in conjunction with the Medtronic Nexframe Stereotactic System for the precise positioning of microelectrodes and implantable leads. A stereotactic guidance system used in conjunction with…
    Category
    Medical Device
    Distribution
    15 states
  • HighCPSC·14251·2014-08-06

    Vizio Recalls 39- and 42-Inch E-Series Televisions Due to Tip-Over Risk

    Vizio is recalling about 245,000 39- and 42-inch E-Series televisions because the stand assembly can fail, causing the TV to tip over and pose an impact injury risk.

    Product
    VIZIO E-Series 39-inch and 42-inch televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2123-2014·2014-08-06

    Ra Medical Systems Recalls PHAROS EX-308 Excimer Lasers Due to Calibration Defect

    Ra Medical Systems is recalling 435 PHAROS EX-308 Excimer Lasers because they may calibrate with the iris closed.

    Product
    PHAROS Excimer Laser, Model No. EX-308 UVB phototherapy for the treatment of psoriasis, vitiligo, atopic dermatitis and leukoderma
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2241-2014·2014-08-06

    King of Pops Banana Puddin' Recalled for Undeclared Soy and Wheat

    King of Pops is recalling Banana Puddin' pops due to undeclared soy and wheat allergens. Consumers with allergies should not consume the product.

    Product
    King of Pops Banana Puddin', frozen flavored pop cycle, Net Wt. 3.2oz., Hand Made by King of Pops, 4845 Chateau Ave., Unit D, Charleston, SC 29405
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2130-2014·2014-08-06

    Teleflex Recalls RUSCH TruLite Disposable Laryngoscope Handles

    Teleflex Medical is recalling RUSCH TruLite laryngoscope handles because the handle may heat up and melt the end cap.

    Product
    RUSCH, TruLite, One-Piece Disposable Laryngoscope Handle Blade Combination, Non-Sterile, Rx Only, Distributed by: Teleflex Medical.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2126-2014·2014-08-06

    Baxter Recalls FlowCOUPLER Implantable Devices for Potential Signal Loss

    Baxter Healthcare is recalling 1,315 FlowCOUPLER implantable devices because some units may lose electrical continuity, preventing proper monitoring of blood flow.

    Product
    FlowCOUPLER. An implantable device that is used to detect blood flow in vessels. Used in the end-to-end anastomosis of veins and arteries normally encountered in microsurgical and vascular reconstructive procedures. The FlowCOUPLER System is intended to detect blood flow and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2238-2014·2014-08-06

    Whole Foods Caesar Salad Mini Recalled for Undeclared Allergens

    Whole Foods Market Group Inc. is recalling Caesar Salad Mini products due to switched labels that failed to declare tree nuts and fish.

    Product
    Whole Foods Caesar Salad Mini Net Wt 4 0z plastic shell
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2240-2014·2014-08-06

    King of Pops Key Lime Pie Recalled for Undeclared Soy and Wheat

    King of Pops is recalling Key Lime Pie frozen pops due to undeclared soy and wheat allergens. Consumers with allergies should not consume the product.

    Product
    King of Pops Key Lime Pie, frozen flavored pop cycle, Net Wt. 3.2oz., Hand Made by King of Pops, 4845 Chateau Ave., Unit D, Charleston, SC 29405
    Category
    Food
    Distribution
    1 state
  • HighCPSC·14250·2014-08-05

    Samson International Recalls Spencer Bar Stool Due to Fall Hazard

    Samson International is recalling Spencer Bar Stools sold at Costco because the footrest can crack, posing a fall hazard. No injuries have been reported.

    Product
    Spencer Bar Stool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14249·2014-08-05

    Scubapro Aladin2 Dive Computers Recalled for Decompression Sickness Risk

    Johnson Outdoors Diving is recalling Scubapro Aladin2 dive computers because they may leak and stop working, posing a risk of injury from decompression sickness.

    Product
    Scubapro Aladin2 dive computers, commonly referred to as Aladin Square dive computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V475000·2014-08-04

    Toyota Recalls FJ Cruiser and Tacoma for Incorrect Tire Placard Information

    Toyota is recalling 2008-2014 FJ Cruiser and Tacoma vehicles with specific accessory wheels because the tire placard may list incorrect spare tire size or inflation pressure.

    Product
    TOYOTA — TOYOTA FJ CRUISER, TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V473000·2014-08-01

    Nova Bus Recalls 2013 LFS Transit Buses for Wiper Linkage Bolt Issue

    Nova Bus is recalling 189 model year 2013 LFS transit buses because a windshield wiper linkage bolt may loosen, potentially rendering wipers inoperable and increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide