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.

39151–39175 of 50506

  • HighFDA (Drugs)·D-0482-2015·2015-04-15

    Hospira Recalls Ketorolac Tromethamine Injection Due to Crystallization

    Hospira Inc. is voluntarily recalling specific lots of Ketorolac Tromethamine Injection because of crystallization. The affected vials were distributed nationwide and in Guam and Singapore.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1941-2015·2015-04-15

    Iberia Sazon Seasoning Recalled for Undeclared Peanut Protein

    Iberia Foods is recalling Sazon Iberia seasoning because it may contain undeclared peanut protein. Consumers should check lot numbers and stop using the product.

    Product
    SAZON IBERIA CON CULANTRO Y ACHIOTE Coriander & Annatto: 1) NET WT. 3.52 OZ. 100g, 18/20 PACKS, UPC 0 75669 10832 9, 2) NET WT. 6.34 OZ. 180g, 15/36 PACKS, UPC 0 75669 10831 2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1378-2015·2015-04-15

    Carestream CS 8100 3D Dental X-Ray Devices Recalled for Unexpected Head Descent

    Carestream Health is recalling 470 CS 8100 3D dental X-ray units because the device head may descend unexpectedly, posing a risk of injury to patients or operators.

    Product
    CS 8100 3D, CATALOG # (s): 5311162, 5311188. Intended to produce complete or segmented tomographic digital panoramic X-ray images and three-dimensional digital X-ray images of the dentomaxillo-facial area to be used at the direction of healthcare professionals as diagnostic…
    Category
    Medical Device
    Distribution
    46 states
  • HighFDA (Devices)·Z-1394-2015·2015-04-15

    Toshiba INFX-8000V Interventional Angiography System Recall for Brake Defect

    Toshiba is recalling 28 INFX-8000V Interventional Angiography Systems because the table base rotational brake may not engage when force is applied to the table top.

    Product
    INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1382-2015·2015-04-15

    Intuitive Surgical Recalls da Vinci S Camera Drapes Due to Waxy Appearance

    Intuitive Surgical is recalling da Vinci S Camera Drapes because they may have a cloudy or waxy appearance that could transfer to patients or tear.

    Product
    da Vinci S Surgical System IS2000, Camera Drape, 20 Pack. Microtek Medical Equipment Drapes are to be used to cover a variety of surgical and non-surgical equipment in various settings throughout the clinical setting.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·15V224000·2015-04-15

    Thor Motor Coach Recalls 2016 Motorhomes for Missing Weight Label

    Thor Motor Coach is recalling 168 model year 2016 motorhomes because the Occupant and Cargo Carrying Capacity label may be missing water weight information, creating an overload risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR CHATEAU, OUTLAW, CITATION, SIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1384-2015·2015-04-15

    Intuitive Surgical Recalls da Vinci S Monitor Drapes Due to Waxy Appearance

    Intuitive Surgical is recalling da Vinci S Vision-Cart Monitor Drapes because they may have a cloudy or waxy appearance that could transfer to patients or tear.

    Product
    da Vinci S Surgical System IS2000, Vision-Cart Monitor Drape, 20 Pack. Microtek Medical Equipment Drapes are to be used to cover a variety of surgical and non-surgical equipment in various settings throughout the clinical setting.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-1381-2015·2015-04-15

    Intuitive Surgical Recalls da Vinci S Camera Arm Drapes

    Intuitive Surgical is recalling da Vinci S Camera Arm Drapes due to a cloudy or waxy appearance that may transfer to patients or cause the drape to tear.

    Product
    da Vinci S Surgical System IS2000, Camera Arm Drape, 20 Pack. Microtek Medical Equipment Drapes are to be used to cover a variety of surgical and non-surgical equipment in various settings throughout the clinical setting.
    Category
    Medical Device
    Distribution
    1 state
  • HighCPSC·15109·2015-04-14

    San Pedro Manufacturing Recalls Renovated Mattresses and Foundations

    San Pedro Manufacturing is recalling about 4,800 renovated mattresses and foundations because they fail to meet federal fire safety standards.

    Product
    Mattresses and Mattresses with Foundations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·059-2015·2015-04-11

    Corn Maiden Foods Recalls Beef and Pork Products for Undeclared Soy Allergen

    Corn Maiden Foods is recalling approximately 15,600 pounds of pork and beef products because they contain undeclared hydrolyzed soy protein, a known allergen.

    Product
    Corn Maiden Foods, Inc. — Corn Maiden Foods, Inc. Recalls Beef and Pork Products Due To Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1364-2015·2015-04-08

    Biomet Recalls Ziploop Button and ToggleLocs Due to Packaging Seal Issues

    Biomet, Inc. is recalling 50 units of Ziploop Buttons and ToggleLocs manufactured in 2014 because sterile packaging was not properly sealed.

    Product
    Ziploop Button Product Usage: The Ziploop Button is a non-resorbable system intended to aid in ACL reconstructive procedure due to injury or degenerative disease
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1797-2015·2015-04-08

    San Juan Salsa Recalls Six Varieties Due to Peanut Contamination

    San Juan Salsa Co. is recalling six varieties of salsa because they may contain peanuts. The salsa was distributed within Washington.

    Product
    Mild Salsa, 14 oz; product is packaged in clear plastic tub with plastic lid, labeled in part, "***SAN JUAN SALSA CO.***MILD***Keep Refrigerated***NET WT. 14 oz (397 g)***SAN JUAN SALSA CO. 5919 195TH ST. NE #5, ARLINGTON, WA 98223***" UPC code: 7 18738 54632 4
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1854-2015·2015-04-08

    Native Texan Peach Medium Recalled for Undeclared Peanuts

    Creative Foodworks, Inc. is recalling Native Texan Peach Medium due to undeclared peanuts. The product was distributed in five states.

    Product
    Native Texan Peach Medium NET WT. 16oz 453g 1LB. Brought to You by: Native Texan Food Co. box 50583, austin, TX 78763
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1810-2015·2015-04-08

    Tastefully Simple Corn, Black Bean Salsa Recalled for Undeclared Peanuts

    Creative Foodworks, Inc. is recalling Tastefully Simple Corn, Black Bean Salsa because it may contain undeclared peanuts.

    Product
    Tastefully Simple Corn, Black Bean Salsa NET WT 16 OZ (454g); Distributed by Tastefully Simple, Inc. Alexandria, MN 56308
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1840-2015·2015-04-08

    Stagecoach Salsa Recalled for Undeclared Peanuts

    Creative Foodworks, Inc. is recalling Stagecoach Salsa Classic San Antonio Salsas Medium due to undeclared peanuts.

    Product
    STAGECOACH SALSA CLASSIC SAN ANTONIO SALSAS MEDIUM Net Wt. 16 oz. (454g) Manufactured Exclusively for: Stagecoach Salsa Company 25011 Saddle Trail San Antonio, texas 78255
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1838-2015·2015-04-08

    Southern Heat Medium Salsa Recalled for Undeclared Peanuts

    Creative Foodworks, Inc. is recalling Southern Heat medium salsa due to undeclared peanuts. The product was distributed in five states.

    Product
    SOUTHERN HEAT medium salsa NET WT. 16 OZ. (454g) Distributed By: Lone Star Heat Products, Inc. P.O. Box 171572 Arlington, Texas 76003 U.S.A.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1821-2015·2015-04-08

    Fredericksburg Farms Black Bean and Corn Salsa Recalled for Undeclared Peanuts

    Creative Foodworks is recalling Fredericksburg Farms salsa due to undeclared peanuts. Consumers with peanut allergies should not consume the product.

    Product
    Fredericksburg Farms ALL NATURAL AND GLUTEN FREE! Rio Grande Black Bean & Corn Salsa 12 oz. (340g) Mild Distributed By: Fredericksburg Farms, Inc.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-1351-2015·2015-04-08

    Medcomp Recalls Catheter Insertion Kits Due to Sterilization Defect

    Medcomp is recalling specific catheter insertion kits because one biological indicator failed during the sterilization process, potentially compromising sterility.

    Product
    Medcomp Duo-Flow 400XL Catheter, Hemo-Flow Catheter, SLX Catheter, Triple Lumen Infusion Catheter, CT rated PICC, Split Cath III, PC Split Cath III; AngioDynamics product- Dura-Flow Catheter, Schon XL Catheter; The affected product are insertion kits used to implant the…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1809-2015·2015-04-08

    Creative Foodworks Recalls Austin Grand Prize Hot Sauce for Undeclared Peanuts

    Creative Foodworks, Inc. is recalling specific lots of Austin Grand Prize Hot Sauce because the product may contain undeclared peanuts.

    Product
    Austin Grand Prize Hot Sauce; Best of Show Austin-San Antonio Hot Sauce Challenge 1991; Mfg. Exclusively for: Skins N More Inc. 805 E. Court St., Suite #160 Seguin, Texas 78155 (210) 889-2109
    Category
    Food
    Distribution
    5 states