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.

41301–41325 of 50511

  • HighCPSC·14733·2014-05-01

    Altria Recalls 3-in-1 Flashlight Due to Burn and Injury Hazards

    Altria Group Distribution Company is recalling 365,000 Marlboro promotional flashlights because matches can ignite inside the device, posing burn and injury risks.

    Product
    3-in-1 flashlight, compass and match holder
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14732·2014-05-01

    J. Crew Recalls Baby Coveralls Due to Choking Hazard

    J. Crew is recalling approximately 8,700 baby coveralls because snaps can detach, posing a choking hazard to young children.

    Product
    Baby Coveralls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1503-2014·2014-04-30

    Philips Digital Diagnost Radiographic System Recall Due to Footboard Defect

    Philips is recalling 985 Digital Diagnost stationary radiographic systems because the footboard may not be securely held if the fix clamp is not correctly adjusted.

    Product
    Digital Diagnost, stationary radiographic system; Models: 712020/22/25/26/50/52/54/55/57/60/62/80/81/82/85
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V223000·2014-04-30

    GM Recalls 2014 Buick, Chevrolet, and GMC SUVs for Fuel Gauge Error

    General Motors is recalling 51,640 model year 2014 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because engine software may cause the fuel gauge to read inaccurately.

    Product
    CHEVROLET — CHEVROLET, GMC, BUICK TRAVERSE, ACADIA, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1493-2014·2014-04-30

    Stryker PenAdapt Electrosurgical Accessory Recalled for Sterile Barrier Breach

    Stryker is recalling 35,310 PenAdapt electrosurgical accessories due to packaging cuts that may breach the sterile barrier and the presence of aluminum shavings.

    Product
    Stryker PenAdapt"; Rx Only, Sterile. This device is an accessory to an electrosurgical unit (ESU). The PenAdapt is used to remove smoke, particles, and body and casual fluids from the point of surgical activity during surgical procedures that use ESU for cutting and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1509-2014·2014-04-30

    Teleflex Recalls Monodek Violet Synthetic Absorbable Surgical Sutures

    Teleflex Medical is recalling Monodek Violet Synthetic Absorbable Surgical Sutures because they do not meet minimum knot tensile strength requirements.

    Product
    Monodek Violet Synthetic Absorbable Surgical Sutures, MF 0 TC43/HR26 48
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1476-2014·2014-04-30

    BioMerieux Recalls FB Reagent Due to False Negative Test Results

    BioMerieux SA is recalling FB Reagent (REF 70562) and ZYM B reagent (REF 70493) because a visual defect and activity issue can cause false negative results in Rapid ID 32 and API biochemical tests.

    Product
    FB Reagent (REF 70562). FB reagent is an additional test used for revealing the results of some miniaturized biochemical test included in the API and Rapid ID 32 strips. The API and ID 32 strips product lines are a standardized system combining several biochemical tests…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1474-2014·2014-04-30

    Remel Recalls Oxoid Legionella Pneumo Groups 2-14 Test Kits

    Remel Inc is recalling two boxes of Oxoid Legionella Pneumo Groups 2-14 test kits because a reagent may produce false negative results.

    Product
    Oxoid Legionella Pneumo Groups 2-14, DR0802M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.
    Category
    Medical Device
    Distribution
    11 states
  • HighNHTSA·14V226000·2014-04-30

    Glaval Transit Bus Recall for Wheelchair Lift Cable Fire Risk

    Glaval is recalling 2007-2012 transit buses equipped with certain Ricon wheelchair lifts. An armored cable may not clear the lift, potentially causing a short circuit and fire.

    Product
    GLAVAL BUS — GLAVAL BUS, GLAVAL ENTOURAGE, CONCORDE, APOLLO, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1495-2014·2014-04-30

    Philips MDC PACS and IntelliSpace PACS DCX Software Recall for Density Errors

    Philips is recalling MDC PACS and IntelliSpace PACS DCX software because it may display incorrect density measurements on Enhanced CT and MR examinations.

    Product
    Philips MDC PACS R2.X / IntelliSpace PACS DCX R3.1 software, software application that is used for receiving, managing, archiving, distributing and recording medical images onto portable digital media (including but not limited to Compact Disk and DVD). The MDC…
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-1473-2014·2014-04-30

    Remel Recalls Oxoid Legionella Latex Test Due to False Negative Risk

    Remel Inc is recalling specific lots of Oxoid Legionella Latex Test kits because a reagent may produce false negative results.

    Product
    Oxoid Legionella Latex Test, DR0800M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-1875-2014·2014-04-30

    CJ Bakery Recalls Cinnamon Manjoo Cookies for Undeclared Wheat

    CJ Bakery is recalling Cinnamon Cookie Manjoo products because they contain undeclared wheat, a major food allergen.

    Product
    Cinnamon Cookie Manjoo, 200g Net Weight. Packaged in clear plastic bag, 10 per bag. Product package labeled in part:"***Cinnamon Cookie (Manjoo)*** Net Wt. 200g, 7.1oz***Manufactured by: CJ Foodville USA, Inc. (323)480-9105***6834 E. Slauson Ave, Commerce, CA…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1488-2014·2014-04-30

    GE Vivid E9 Ultrasound System Recalled for Probe Overheating Risk

    GE Healthcare is recalling Vivid E9 Ultrasound Systems because incorrect power settings for four specific probe types may cause them to overheat.

    Product
    GE Vivid E9 Ultrasound System, a general-purpose ultrasound system, specialized for use in cardiac imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1877-2014·2014-04-30

    CJ Bakery Recalls Chocolate Madelines Due to Undeclared Wheat

    CJ Bakery is recalling chocolate madelines, madelines, and cinnamon manjoo because they contain undeclared wheat.

    Product
    Chocolate Madeline, 80g Net Weight. Packaged in clear plastic bag, 4 per bag. Product package labeled in part:"AUTHENIC BAKERY TOUS Les JOURS***Madeline*** Net Wt. 80g, 2.8oz ***Manufactured by: CJ Foodville USA, Inc. (323)480-9105***6834 E. Slauson Ave, Commerce, CA…
    Category
    Food
    Distribution
    6 states
  • HighCPSC·14165·2014-04-30

    Horizon Hobby Recalls Blade 700 X Helicopter Kits Due To Injury Hazard

    Horizon Hobby is recalling Blade 700 X Pro Series helicopter kits and spindle sets because a defective washer can cause rotor blades to detach, posing an injury risk.

    Product
    Radio-controlled helicopter kits and spindle sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1506-2014·2014-04-30

    Teleflex Recalls Sengstaken Tubes Due to Sterility Concerns

    Teleflex Medical is recalling Sengstaken and Sengstaken-Blakemore tubes because the sterility of the product cannot be guaranteed.

    Product
    Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800, 204802, and 204803, a gastrointestinal tube and accessories, consisting of flexible or semi-rigid tubing used for instilling fluids into, withdrawing fluids from, splinting, or suppressing bleeding…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1876-2014·2014-04-30

    CJ Bakery Recalls Madeline and Manjoo Products for Undeclared Wheat

    CJ Bakery is recalling specific baked goods due to undeclared wheat, posing a risk to individuals with wheat allergies or celiac disease.

    Product
    Madeline, 80g Net Weight. Packaged in clear plastic bag, 4 per bag. Product package labeled in part:"AUTHENIC BAKERY TOUS Les JOURS***Madeline*** Net Wt. 80g, 2.8oz ***Manufactured by: CJ Foodville USA, Inc. (323)480-9105***6834 E. Slauson Ave, Commerce, CA…
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-1478-2014·2014-04-30

    BioMerieux Recalls ZYM B and FB Reagents Due to False Negative Results

    BioMerieux is recalling ZYM B and FB reagents because a visual defect and activity issue caused false negative results in Rapid ID 32 strips and API biochemical tests.

    Product
    API Listeria (REF 10300). ZYM B reagent is used and included inside of API NH (REF 10400) and API Listeria (10300). All of the APIs are standardized systems combining several biochemical tests that enable group or species identification of most microorganisms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1885-2014·2014-04-30

    Jolly Time Microwave Popcorn Recalled for Metal Fragments

    American Pop Corn Co is recalling Jolly Time Microwave popcorn due to potential contamination with stainless steel metal fragments.

    Product
    Jolly Time Microwave popcorn, Homemade Classic Stovetop Flavor, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190007807, on the 12-ct case - UPC 10028190007804, 48-ct shipper UPC 128190487804 American Pop Corn Company, Sioux City, IA
    Category
    Food
    Distribution
    22 states
  • HighFDA (Food)·F-1884-2014·2014-04-30

    Jolly Time Microwave Popcorn Recalled for Metal Fragment Contamination

    American Pop Corn Co is recalling Jolly Time Extra Butter microwave popcorn due to potential contamination with stainless steel metal fragments.

    Product
    Jolly Time Microwave popcorn, Extra Butter, 3/3-oz bags/carton. The cartons are packaged 12-cartons/case. Individual carton - UPC 028190008477, on the 12 count case - UPC 10028190008474 and 48 ct shipper with UPC 128190488474 American Pop Corn Company, Sioux City, IA.
    Category
    Food
    Distribution
    22 states
  • HighCPSC·14731·2014-04-29

    Kawasaki Recalls 2014 Off-Road Motorcycles Due to Crash Hazard

    Kawasaki is recalling about 611 model year 2014 KLX110 and KLX110L off-road motorcycles because camshaft sprocket bolts can loosen, causing the engine to lock and creating a crash hazard.

    Product
    Off-Road Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14T003000·2014-04-25

    Lionshead Recalls Vail Sport ST LH 99 Trailer Tires for Missing Markings

    Lionshead Specialty Tire & Wheel LLC is recalling approximately 4,000 Vail Sport ST LH 99 trailer tires manufactured between April 2012 and February 2013 because they may lack required load range markings.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide