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.

32826–32850 of 50502

  • HighFDA (Devices)·Z-1498-2017·2017-03-29

    Merge Eye Station Import Utility Recalled for System Lockup Risk

    Merge Healthcare is recalling the Eye Station Import Utility software because system lockups may cause patient injury or delay diagnosis.

    Product
    Merge Eye Station Import Utility (ESIU). The firm name on the labeling is Merge Healthcare.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1242-2017·2017-03-29

    Route 11 Sour Cream & Chive Potato Chips Recalled for Salmonella Risk

    Small Fry Inc. is recalling Route 11 Sour Cream & Chive Potato Chips because an ingredient, nonfat dry milk powder, was found to contain Salmonella.

    Product
    Route 11 Sour Cream & Chive Potato Chips2 oz bag (30/cs) Route 11 Sour Cream & Chive Potato Chips6 oz bag (12/cs)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1517-2017·2017-03-29

    Merge Healthcare Recalls Merge Cardio Software Due to Data Integrity Issues

    Merge Healthcare is recalling Merge Cardio software versions 9.0 through 9.0.8 because users can merge device files with confirmed reports, potentially adding unverified information.

    Product
    Merge Cardio software. Product Usage: Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1627-2017·2017-03-29

    Diamond Crystal Cocoa Powder Recalled for Potential Metal Contamination

    Diamond Crystal Brands is recalling Chef's Companion Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.

    Product
    Natural Cocoa Powder 22-24% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand name: Chef's Companion: 1 bag /case, UPC 10719098582240; Diamond Crystal Brands, Inc. Savannah, GA 31405
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1499-2017·2017-03-29

    Stanley Security Recalls 500 Arial Wireless Call Pendants

    Stanley Security Solutions is recalling 500 Arial Wireless Water-Resistant Call Pendants because they were incorrectly programmed, which may prevent alarms from sounding when the button is pressed.

    Product
    Arial Wireless Water-Resistant Call Pendant The Arial Pendant tag is part of the Arial wireless emergency call management system. It enables residents in assisted living, skilled nursing or independent living to call staff with the press of a button.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1494-2017·2017-03-29

    Nidek EC-5000 Excimer Laser Software Recall for Unintended Correction Programming

    Nidek Inc is recalling Final Fit Software versions 1.11 and 1.12 for the EC-5000 Excimer Laser System because treatment planning could be programmed with an unintended correction.

    Product
    Final Fit Software Version 1.11 and 1.12; PC Based software installed outside Nidek EC-5000 Excimer Laser System. Ophthalmic laser system use for correction of corneal refraction and ablation of the corneal surface. The system is composed of a laser generator which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1626-2017·2017-03-29

    Diamond Crystal Cocoa Powder Recalled for Potential Metal Contamination

    Diamond Crystal Brands is recalling specific lots of Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.

    Product
    Natural Cocoa Powder 10-12% cocoa butter, Net Wt. 5 lbs. (2.27 kg) packaged under the following brand names: Monarch distributed by U.S. Foodservice UPC 50758108102533; Chef's Companion: 1 bag /case, UPC 10719098582233; and 6 bags/case, UPC 50719098582293 Diamond Crystal…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1669-2017·2017-03-29

    Carriage House Creations Recalls Bourbon Basting Sauce for Undeclared Allergens

    Carriage House Creations is recalling specific varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy.

    Product
    Carriage House Creations; Bold N' Spicy Bourbon Basting Sauce; Net wt. 12 Ounces; Carriage House Creations, 544 Gordon Alley; Reynoldsville, PA 15851;
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·17V217000·2017-03-29

    2016 Thomas Built Buses Saf-T-Liner C2 Recalled for Transmission Defect

    Daimler Trucks North America is recalling one 2016 Thomas Built Buses Saf-T-Liner C2 school bus because the transmission grade brake may fail to deactivate, increasing crash risk in slippery conditions.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1670-2017·2017-03-29

    Carriage House Creations Recalls Bourbon Basting Sauce for Undeclared Allergens

    Carriage House Creations is recalling specific varieties of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy.

    Product
    Carriage House Creations; Bourbon Basting Sauce Hot; Net wt. 12 Ounces; Carriage House Creations, 544 Gordon Alley; Reynoldsville, PA 15851;
    Category
    Food
    Distribution
    1 state
  • HighCPSC·17120·2017-03-29

    Juratoys Recalls Janod Push Toy Trolleys Due to Impact Injury Hazard

    Juratoys is recalling four models of Bricolo by Janod push toy trolleys because they can tip backwards, posing an impact injury hazard to children.

    Product
    Bricolo by Janod ® Push toy trolleys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1496-2017·2017-03-29

    Merge Cardio software recall due to patient data display error

    Merge Healthcare is recalling Merge Cardio software versions with IPID because the system may display images from different patients as if they belong to the same individual.

    Product
    Merge Cardio software with Issuer of Patient ID (IPID). The firm name on the label is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-1668-2017·2017-03-29

    Carriage House Creations Recalls Bourbon Basting Sauce for Undeclared Allergens

    Carriage House Creations is recalling specific batches of Bourbon Basting Sauce and Hot BBQ Sauce due to undeclared peanuts and soy.

    Product
    Carriage House Creations; Bourbon Basting Sauce Mild; Net wt. 12 Ounces; Carriage House Creations, 544 Gordon Alley; Reynoldsville, PA 15851;
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1513-2017·2017-03-29

    Medtronic Poly Component Trial Knee Implants Recalled for Cracked Dovetails

    Medtronic Sofamor Danek USA Inc is recalling 72 units of Poly Component Trial knee implants because the dovetails were observed as cracked or broken.

    Product
    Poly Component Trial, MPCS, packaged in the following sizes and configurations: a) Poly Component Trial - MPCS 3x10L, REF 90-SRK-192310 b) Poly Component Trial - MPCS 3x10R, REF 90-SRK-191310 c) Poly Component Trial - MPCS 3x12L, REF 90-SRK-192312 d) Poly Component Trial…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1691-2017·2017-03-29

    Lakeside Foods Recalls Frozen Peas and Beans for Listeria Risk

    Lakeside Foods is voluntarily recalling frozen green beans, peas, and peas/carrots due to potential Listeria monocytogenes contamination.

    Product
    Harris Teeter, Sweet Green Peas, 12 oz (340g), UPC 007203671652
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1539-2017·2017-03-29

    Integra Recalls Panta Nails Due to Potential Sterility Seal Issues

    Integra LifeSciences is voluntarily recalling Panta and Panta XI Nails because package seals may not maintain intended sterility.

    Product
    Panta Nail, Rx only, Sterile,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1516-2017·2017-03-29

    Medtronic Recalls Poly Component Trials Due to Cracked or Broken Dovetails

    Medtronic is recalling 111 units of Poly Component Trials because the dovetails were observed as cracked or broken.

    Product
    Poly Component Trial, PS, packaged in the following sizes and configurations: a) Poly Component Trial - PS 3x10, REF 90-SRK-180310 b) Poly Component Trial - PS 3x12, REF 90-SRK-180312 c) Poly Component Trial - PS 3x14, REF 90-SRK-180314 d) Poly Component Trial - PS 4x10…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1717-2017·2017-03-29

    Chapis Spice & Tea Recalls Bread Crumbs for Undeclared Allergens

    Chapis Spice & Tea is recalling Pan Molido Natural Bread Crumbs due to undeclared allergens including wheat, milk, eggs, tree nuts, and soybean.

    Product
    Pan Molido Natural Bread Crumbs, Net Wt. 6oz and 12oz
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1714-2017·2017-03-29

    Country Fresh Marketside Stuffed Baby Bellas Recalled for Listeria Risk

    Country Fresh Inc. is recalling Marketside Garlic & Four Cheese Stuffed Baby Bellas due to possible Listeria monocytogenes contamination.

    Product
    Marketside Garlic & Four Cheese Stuffed Baby Bellas Net Wt. 7 oz. (198g) Distributed By: Wal-Mart Stores, Inc., Bentonville, AR 72716 UPC: 681131148214
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1642-2017·2017-03-29

    Manzana Recalls Trader Joe's Apple Sauce Due to Glass Fragments

    Manzana Products Co. is recalling Trader Joe's Organic Unsweetened Apple Sauce after customer complaints and inspections revealed small pieces of glass in the product.

    Product
    Trader Joe's Organic Unsweetened Apple Sauce; 24 oz. glass jar. Best Before date stamped on top of lid. UPC: 00194877 Distributed by Trader Joe's, Monrovia, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1712-2017·2017-03-29

    Country Fresh Stuffed Mushrooms Recalled for Possible Listeria Contamination

    Country Fresh Inc. is recalling Stuffed Mushrooms due to possible Listeria monocytogenes contamination. The product was distributed in ten southeastern and southern states.

    Product
    Country Fresh Creations Stuffed Mushrooms Net Wt. 7 oz. (198g) Packed Regionally by Country Fresh LLC Headquarters, Conroe, TX 77384 www.countryfreshinc.com UPC: 074641072078
    Category
    Food
    Distribution
    10 states