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.

33226–33250 of 50502

  • HighFDA (Devices)·Z-1142-2017·2017-02-15

    Merge Healthcare Recalls Eye Station Imaging Devices Due to Capture Failures

    Merge Healthcare is recalling 182 Eye Station capture stations because they may fail to capture eye images as intended, posing a risk to patient health.

    Product
    Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager distributed by Ophthalmic Imaging Systems (OIS). Model number 136 T1700 Capture Stations & 46 T5810 Capture Stations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1148-2017·2017-02-15

    AtriCure Recalls AtriClip LAA Exclusion System Due to Jaw Breakage

    AtriCure is recalling 464 AtriClip LAA Exclusion System devices because a complaint was received regarding the PRO2 jaw breaking prior to surgery.

    Product
    AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a conventional thermoformed polyethylene terephthalate glycol (PETG) tray with a Tyvek¿ lid. A single-walled non-corrugated box completes the single unit package. Six (6)…
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-1176-2017·2017-02-15

    Merge PACS Software Recalled for Potential Incorrect Patient Image Display

    Merge Healthcare is recalling Merge PACS software version 7.0.1 because it may display incorrect patient images, potentially delaying diagnosis or treatment.

    Product
    Merge PACS software. The firm name on the label is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-1452-2017·2017-02-15

    Taylor Farms Rotini Pasta Salad Recalled for Undeclared Wheat Allergen

    Taylor Farms is recalling 10 oz. Rotini Pasta Salad containers because the label incorrectly identifies the product as mustard potato salad, failing to declare the wheat allergen.

    Product
    Fresh Foods Market Delicatessen Rotini Pasta Salad; Net Wt. 10 oz . (283g) Clamshell package. UPC Code: WO2017019 Perishable; Keep Refrigerated; Distributed by The Kroger Col., Cincinnati, OH
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1450-2017·2017-02-15

    Circle U Foods Recalls Deli Sauce Seasoning Due to Glass Inclusion

    Circle U Foods is recalling 12 cases of Elmer's Deli Sauce Seasoning due to a potential glass inclusion. The product was distributed in Texas, Illinois, Kansas, and North Carolina.

    Product
    Circle U Foods, Inc. Product Code: 211013 NPP/Elmer's Deli Sauce Seasoning Pounds Per Bag/Box: 25.00 Lbs.
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1177-2017·2017-02-15

    Teleflex Recalls Sheridan Cuffed Tracheal Tubes Due to Labeling Inconsistency

    Teleflex Medical is recalling Sheridan cuffed tracheal tubes because some units are labeled with incorrect sizes, potentially leading to improper airway management.

    Product
    Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A tracheal tube is inserted into a patients mouth or nose for airway management
    Category
    Medical Device
    Distribution
    38 states
  • HighFDA (Food)·F-1440-2017·2017-02-15

    Dannon Dairy Drink Recalled for Incorrect Walnut Allergen Labeling

    Dannon is recalling specific bottles of Dairy Drink Nut and Cereal because the label incorrectly lists walnut as an ingredient and allergen, while the product actually contains pecan.

    Product
    DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421
    Category
    Food
    Distribution
    18 states
  • HighNHTSA·17V096000·2017-02-14

    Thor Motor Coach Recalls 2014-2016 Motorhomes for Wiper Defect

    Thor Motor Coach is recalling 2,483 motorhomes because improperly installed windshield wipers may fail, reducing visibility and increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR PALAZZO, TUSCANY, TUSCANY XTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17087·2017-02-13

    Target Recalls Threshold Patio Benches Due to Fall Hazard

    Target is recalling about 1,300 Threshold patio benches because they can collapse while in use, posing a fall hazard.

    Product
    Threshold patio benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V087000·2017-02-09

    BMW Recalls 2014 X1 Models for Battery Cable Connection Defect

    BMW is recalling 2014 X1 vehicles because battery positive cables may develop high resistance, potentially causing engine stalls and increasing crash risk.

    Product
    BMW — BMW X1 SAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17084·2017-02-09

    Feld Entertainment Recalls Light-Spinner Toy Wands Due to Injury Hazard

    Feld Entertainment is recalling light-spinner toy wands sold at Disney shows because a top component can detach, exposing a metal rod that poses an injury risk to young children.

    Product
    Light-spinner toy wands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0459-2017·2017-02-08

    VistaPharm Recalls Metoclopramide Oral Solution Due to Potential Water Contamination

    VistaPharm is recalling specific lots of Metoclopramide Oral Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Metoclopramide Oral Solution, USP 10 mg/ 10 mL, 50 unit dose cups of 10 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-031-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1108-2017·2017-02-08

    PerkinElmer Spare Disk Remover Module Recall Due to Corrosion Risk

    PerkinElmer is recalling Spare Disk Remover Modules because defective axles may corrode in humid conditions, potentially contaminating test plates.

    Product
    Spare Disk Remover Module; Product Number: 61001820 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
    Category
    Medical Device
    Distribution
    4 states
  • HighNHTSA·17V080000·2017-02-08

    Mercedes-Benz Recalls 2017 Models for Air Bag Ignition Failure

    Mercedes-Benz is recalling 2017 E300, E400, E550, GLA 250, and CLA250 vehicles because the pelvis or front passenger air bag inflator may fail to ignite in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300, E400, GLA 250, CLA250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1110-2017·2017-02-08

    Biom'up Recalls Renovix Collagen Membranes Due to Sterility Assurance Concerns

    Biom'up is recalling 1,682 units of Renovix Guided Healing Collagen Membranes due to a lack of sterility assurance. The products were distributed to a sole distributor in North Carolina.

    Product
    RENOVIX Guided Healing Collagen Membrane Intended for use in oral surgical procedures.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1107-2017·2017-02-08

    PerkinElmer Genetic Screening Processor Recalled for Corroding Axles

    PerkinElmer is recalling 24 Genetic Screening Processor instruments because defective ball bushing axles may corrode in humid conditions, risking contamination of sample wells.

    Product
    Genetic Screening Processor (GSP); PerkinElmer Part Number= 2021-0010 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1122-2017·2017-02-08

    Mevion S250 Proton Therapy Units Recalled for Data Loss Error

    Mevion Medical Systems is recalling two S250 Proton Radiation Therapy units because a software error can cause Delta corrections to be lost.

    Product
    MEVION S250-Proton Radiation Therapy Product Usage: Proton Radiation Therapy
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1364-2017·2017-02-08

    Rich Products Recalls Ice Cream Layer Cakes Due to Undeclared Walnuts

    Rich Products Corp. is recalling specific Jon Donaire Ice Cream Layer Cakes because they may contain undeclared walnuts from a supplier.

    Product
    Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy vanilla ice cream, NET WT 4 LB 8 OZ, KEEP FROZEN, UPC 0 49800 62878 6 (retail), Product Code 62878, and UPC 0 49800 02453 3 (retail), Product Code 02453 --- Rich Products Corp., Buffalo, NY 14213…
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1128-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled for Sterility Compromise

    Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall affects 180 units distributed worldwide.

    Product
    Intact Disposable Wands (part of the Intact System) 777-112: 5 Pack 12mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide