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.

35876–35900 of 50504

  • HighFDA (Devices)·Z-1601-2016·2016-05-11

    Siemens Syngo Dynamics PACS Software Recall for Workflow Error

    Siemens is recalling 84 units of Syngo Dynamics software due to a defect that may cause old measurements to be carried forward into new reports.

    Product
    Syngo Dynamics; Kinetdx Picture Archiving and Communications System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1589-2016·2016-05-11

    GE Revolution CT Recalled for Potential X-Ray Tube Loosening

    GE Medical Systems is recalling 26 Revolution CT systems worldwide because a manufacturing error may cause the X-ray tube to loosen, leading to scan errors or image artifacts.

    Product
    GE, Revolution CT. The system is intended for head, whole body, cardiac, and vascular X-ray Computed Tomography applications
    Category
    Medical Device
    Distribution
    4 states
  • HighNHTSA·16V289000·2016-05-11

    Pacific Coachworks Recalls 2016 Rage'N Toy Haulers for Label Error

    Pacific Coachworks is recalling 2016 Rage'N toy haulers because an incorrect Cargo Carrying Capacity value on the Federal Information label could lead to overloading.

    Product
    PACIFIC COACHWORKS — PACIFIC COACHWORKS RAGE'N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16158·2016-05-11

    Bosch Small Angle Grinders Recalled for Overheating and Burn Risk

    Robert Bosch Tool Corp. is recalling about 91,000 Bosch 1380 Slim small angle grinders because they can overheat, melt brush covers, and expose hot components, posing a burn risk.

    Product
    Bosch small angle grinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1596-2016·2016-05-11

    bioMerieux Recalls VITEK 2 Gram Positive Susceptibility Test Cards

    bioMerieux is recalling VITEK 2 Gram Positive Susceptibility Test Cards because they may produce false susceptible results for specific bacteria to Minocycline.

    Product
    VITEK 2 Gram Positive Susceptibility Test Cards (AST-P605), REF 22 325. 20 Cards/Kit. bioMerieux, Inc, Durham, North Carolina 27712. VITEK 2 is an automated system consisting of instruments, software, and reagent cards designed for the identification and antimicrobial…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1293-2016·2016-05-11

    Emerald Cashew Packs Recalled for Potential Glass Fragments

    Diamond Foods is recalling Emerald 100 Calorie Packs of Cashew Halves & Pieces due to the potential for small glass fragments in the product.

    Product
    Emerald 100 Calorie Packs of Cashew Halves & Pieces, roasted and salted. 7 pack/ 0.62 oz. each (17.5 g). Ingredients: Cashews, Vegetable Oil/Safflower, Sunflower and/or Canola Oil, Salt, Rosemary extract (to preserve freshness: Retail Carton UPC: 0 10300 33324 1; Inner…
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·F-1102-2016·2016-05-11

    Pastry Food Products Recalls Unlabeled Potato Balls for Undeclared Allergens

    Pastry Food Products Inc. is recalling unlabeled Rellenos de Papa in Puerto Rico due to undeclared yellow #5, soy protein, and sodium bisulfite.

    Product
    Rellenos de Papa (meat flavored potato balls): This product is distributed without label.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1319-2016·2016-05-11

    Vaughan Foods Recalls La Fiesta Bean Salad for Undeclared Wheat

    Vaughan Foods is recalling La Fiesta Bean Salad tubs because they contain undeclared wheat. The product was distributed in five states.

    Product
    La Fiesta Bean Salad (2/5 LB Tubs) Made By Fresh Creative Foods Moore, OK 73160 UPC 013454371763 packaged in white plastic tub with lid
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·16V276000·2016-05-10

    Elpers Truck Equipment Recalls Cranes Due to Valve Bank Cover Defect

    Elpers is recalling 35 trucks equipped with IMT cranes because the valve bank cover may crack and fall off, creating a road hazard.

    Product
    ELPERS — ELPERS FORD F-450 W/ CRANE, INTL MAXFORCE W/ CRANE, FORD F-550 W/ CRANE, INTL 4300 W/ CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V280000·2016-05-10

    Newmar Recalls 2014-2015 Motorhomes for Power Steering Hose Failure Risk

    Newmar is recalling 93 Essex, Mountain Aire, and London Aire motorhomes because power steering hoses may fail due to high fluid temperatures, increasing crash risk.

    Product
    NEWMAR — NEWMAR ESSEX, MOUNTAIN AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16741·2016-05-10

    Honda Recalls 2016 Pioneer 1000 Off-Highway Vehicles for Door Safety Issue

    American Honda is recalling about 3,300 model year 2016 Honda Pioneer 1000 recreational off-highway vehicles because the front door can open unexpectedly, posing a risk of injury.

    Product
    Recreational off-highway vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16743·2016-05-10

    Bednest Recalls Bedside Infant Sleepers Due to Fall Hazard

    Bednest is recalling bedside infant sleepers manufactured after July 2014 because they fail to meet federal safety requirements, posing a fall hazard to babies.

    Product
    Bedside Sleepers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V275000·2016-05-09

    Spartan Recalls 2012-2015 Utilimaster Aeromaster Vehicles for Wiring Defect

    Spartan Motors is recalling 89 Utilimaster Aeromaster vehicles because a wiring defect may leave the lift gate system powered, posing an injury risk to maintenance personnel.

    Product
    UTILIMASTER — UTILIMASTER AEROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1583-2016·2016-05-04

    Mako Surgical Recalls RESTORIS PST RIO Offset Shell Impactor

    Mako Surgical Corporation is recalling 96 units of the RESTORIS PST RIO Offset Shell Impactor due to a potential disassociation of the orientation pin.

    Product
    RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and implanting acetabular cup components during Total Hip Arthroplasty (THA) surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1584-2016·2016-05-04

    Research Instruments Recalls Integra 3 Micromanipulators Due to Faulty Power Cable

    Research Instruments Ltd is recalling 380 Integra 3 micromanipulators because they were fitted with a potentially faulty power supply cable.

    Product
    Integra 3; Model Numbers: 6-54-100, 6-54-110, 6-54-150, 6-54-160 Product Usage: The Rl TDU500 Micromanipulator for Assisted Reproduction is used to accurately position microtools under a microscope for the techniques of Assisted Reproduction. The Rl Integra is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1130-2016·2016-05-04

    NOW Foods Recalls Elderberry Supplements Due to Undeclared Soy Lecithin

    NOW Foods is recalling 57 bottles of Elderberry 500 mg capsules because they contain undeclared soy lecithin, a common allergen.

    Product
    Elderberry 500 mg packaged in a white and orange bottle containing 60 capsules. The bottle has a blue cap and white lettering.
    Category
    Food
    Distribution
    49 states
  • HighFDA (Food)·F-1248-2016·2016-05-04

    Duncan Hines Swiss Chocolate Cake Mix Recalled for Undeclared Milk

    Pinnacle Foods is recalling Duncan Hines Swiss Chocolate Cake Mix because a natural flavoring containing milk was used, but the product was labeled as non-milk.

    Product
    Duncan Hines Moist Deluxe Swiss Chocolate (Chocolate Suizo) Cake Mix, Net Wt. 16.5 oz. (1 LB 5 oz.) 468 g, Distributed by: Pinnacle Foods, Cherry Hill, New Jersey USA, UPC 6 44209 309748 7
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1554-2016·2016-05-04

    Horiba Recalls ABX Pentra 400 and C400 Clinical Chemistry Analyzers

    Horiba Instruments is recalling ABX Pentra 400 and Pentra C400 analyzers due to malfunctions triggered by specific system alarms.

    Product
    Pentra C400 (version 1.1.2 or lower) The ABX PENTRA 400 and 400C are discrete photometric bench top chemistry analyzers for clinical use. The device is intended to duplicate manual analytical procedures by performing various steps such as pipetting, mixing, heating and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1562-2016·2016-05-04

    GE Healthcare Aisys Anesthesia Machines Recalled for Suction Tubing Defect

    GE Medical Systems is recalling Aisys and Aisys CS2 anesthesia machines because kinked vacuum suction tubing may cause inadequate airway clearance and ventilation.

    Product
    GE Healthcare, Aisys and Aisys CS2. Intended to provide general inhalation anesthesia and ventilator support to a wide range of patients (neonatal, pediatric, and adult).
    Category
    Medical Device
    Distribution
    26 states