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.

41976–42000 of 50511

  • HighFDA (Devices)·Z-0804-2014·2014-01-29

    GE Healthcare Recalls X-Ray Systems with Missing Monitor Suspension Screws

    GE Healthcare is recalling 5,651 X-ray systems worldwide because four outer screws holding the overhead video monitor suspension may be missing. No monitor falls have been reported.

    Product
    Video Monitor Suspensions that may be on the following Fluoroscopic and Radiographic X-Ray systems: Precision 500D, Legacy, Prestilix, Monitrol, RFX, SFX, Tilt-C, Prestige VH, Prestige SI, and Prestige SII Product Usage: The systems are intended to be used as a universal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-857-2014·2014-01-29

    Aidapak Recalls Acyclovir Capsules Due to Potential Labeling Mixup

    Aidapak Services, LLC is recalling 493 Acyclovir 200 mg capsules because they may have been mislabeled as other prescription drugs.

    Product
    ACYCLOVIR, Capsule, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00093894001.
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Drugs)·D-748-2014·2014-01-29

    Novartis Recalls Theraflu Flu and Sore Throat Powder Packets

    Novartis is recalling Theraflu Flu & Sore Throat powder packets because they may contain foreign substances. The recall affects 1.6 million cartons distributed in the US and internationally.

    Product
    Theraflu Flu & Sore Throat (acetaminophen 650 mg, pheniramine maleate 20 mg, phenylephrine hydrochloride 10 mg) powder packets, Natural Apple Cinnamon flavor, 6-count packets per carton, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0818-2014·2014-01-29

    Siemens Recalls Dimension Vista Cyclosporine Flex Reagent Cartridges

    Siemens Healthcare Diagnostics is recalling 1,586 Dimension Vista Cyclosporine Flex reagent cartridges due to complaints about variability in quality control and patient results.

    Product
    Dimension Vista Cyclosporine Flex reagent cartridge an in vitro diagnostic test for the quantitative measurement of cyclosporine A (CSA) in human whole blood on the Dimension Vista System. Measurements are used as an aid in the management of heart, liver, and kidney…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0796-2014·2014-01-29

    Carestream DRX-Evolution X-Ray Systems Recalled for Unexpected Movement

    Carestream Health is recalling DRX-Evolution and Kodak DirectView DR 7500 systems due to a risk of unexpected device movement.

    Product
    DRX-Evolution with FF WS These products are permanently installed diagnostic x-ray systems composed of 4 main components: an operator console, over head tube crane, x-ray tube assembly including a collimator and stationary generator. In addition the device can use an x-ray…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-875-2014·2014-01-29

    Aidapak Recalls Aspirin Tablets Due to Potential Label Mixup

    Aidapak Services, LLC is recalling 81 mg Aspirin DR EC tablets because they may have been mislabeled as Sotalol HCl or Folic Acid.

    Product
    ASPIRIN DR EC, Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00182106105.
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-0781-2014·2014-01-29

    Ranir Recalls TopCare and Up & Up Kids Power Toothbrushes

    Ranir is recalling TopCare and Up & Up kids' power toothbrushes because the tufted disk may detach, posing a choking hazard to children three and younger.

    Product
    TopCare Clifford THE BIG RED DOG power toothbrush for kids!
    Category
    Consumer Product
    Distribution
    2 states
  • HighFDA (Drugs)·D-999-2014·2014-01-29

    Methazolamide Tablets Recalled for Potential Labeling Error

    Aidapak Services is recalling Methazolamide tablets that may have been mislabeled as Buprenorphine HCL due to a label mixup.

    Product
    METHAZOLAMIDE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00781107101.
    Category
    Drug
    Distribution
    4 states
  • HighFDA (Devices)·Z-0806-2014·2014-01-29

    GE Healthcare Recalls Dash Patient Monitors Due to ECG Noise

    GE Healthcare is recalling Dash 3000, 4000, and 5000 patient monitors because cable movement causes intermittent noise on ECG and respiration waveforms, potentially reducing detection performance.

    Product
    GE Healthcare, Dash 3000, Dash 4000 and Dash 5000. Product Usage: The intended use of the system is to monitor physiologic parameter data on adult, pediatric and neonatal patients. K073462: The Dash 3000/4000/5000 patient monitor is intended for use under the direct…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14091·2014-01-28

    Horizon Hobby Recalls Remote Controlled Model Helicopters Due to Injury Hazard

    Horizon Hobby is recalling specific Blade 500 model helicopters because the tail rotor grip can separate, posing a crash and injury risk.

    Product
    Blade 500 X BNF and Blade 500 3D RTF and BNF Remote Controlled Model Helicopters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·007-2014·2014-01-27

    George's Recalls Frozen Chicken Products Due to Undeclared Wheat Allergen

    George's Inc. is recalling approximately 1.25 million pounds of frozen chicken products because wheat, a known allergen, was not declared on the labels.

    Product
    George's Further Processing — Arkansas Firm Recalls Frozen Chicken Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14V016000·2014-01-27

    Winnebago Recalls Trailers With Defective Door Locks That May Jam

    Winnebago is recalling specific 2011-2014 travel trailers and fifth wheels because a defect in the door lock may jam the deadbolt, potentially trapping occupants inside.

    Product
    SUNNYBROOK — SUNNYBROOK, WINNEBAGO BRISTOL BAY, BROOKSIDE, EDGEWATER, REMINGTON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V017000·2014-01-27

    Nu Wa Recalls 2011-2013 Hitchhiker Trailers Due to Door Lock Defect

    Nu Wa Industries is recalling 2011-2013 Hitchhiker fifth wheel trailers because a door lock defect may jam the deadbolt, trapping occupants inside.

    Product
    HITCHHIKER — HITCHHIKER LS, DISCOVER AMERICA, CHAMPAGNE EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V013000·2014-01-24

    PACCAR Recalls Kenworth and Peterbilt Trucks for Seat Belt Defect

    PACCAR is recalling 2014 Kenworth and Peterbilt trucks because seat belt buckles may fail to release, hindering emergency egress.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T370, T660, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14090·2014-01-24

    Ergotron Recalls Interactive Wall Mounts Due to Weld Failure Risk

    Ergotron is recalling interactive wall mounts because a weld can fail, causing the TV to fall. No injuries have been reported, but property damage occurred.

    Product
    Ergotron Interactive Wall Mounts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V012000·2014-01-24

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Door Latch Defect

    PACCAR is recalling 2013-2014 Kenworth T680 and Peterbilt 567/579 trucks because door latches may lock permanently or fail to secure, trapping occupants in emergencies.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 567, 579
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14712·2014-01-23

    Pottery Barn Recalls Morovian Star Pendant Chandeliers Due to Injury Risk

    Pottery Barn is recalling approximately 1,100 Morovian Star Pendant Chandeliers because the joints may fail, causing the fixture to fall. No injuries have been reported.

    Product
    Oversized Morovian Star Pendant Chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14088·2014-01-23

    Suunto Recalls Scuba Air Hoses Due To Drowning Hazard

    Suunto is recalling about 1,300 scuba high-pressure air hoses sold in the U.S. because they may leak or rupture, causing a loss of breathing gas and posing a drowning hazard.

    Product
    Scuba high-pressure air hoses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14087·2014-01-23

    Rayovac Flashlights Recalled by Spectrum Brands Due to Burn Hazard

    Spectrum Brands is recalling specific Rayovac LED flashlights because they can overheat and melt, posing a burn hazard. No injuries have been reported.

    Product
    Rayovac flashlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0740-2014·2014-01-22

    Atrium Oasis Chest Drain Tubing Recalled for Leak or Disconnect Risk

    Atrium Medical Corporation is recalling Oasis Dry Suction Water Seal ATS Chest Drains because the tubing may leak or disconnect.

    Product
    Atrium Oasis Dry Suction Water Seal ATS (Autotransfusion) Blood Recovery System Chest Drain with in-line connectors Product Code: 3650-100. To evacuate air and/or fluid from the chest cavity or mediastinum.
    Category
    Medical Device
    Distribution
    Distributed nationwide