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.

33401–33425 of 50502

  • HighFDA (Food)·F-1235-2017·2017-01-18

    Cheese Club Mac and Cheese Recalled for Salmonella Risk

    Fourth Street Barbecue is recalling Cheese Club mac and cheese products because milk powder ingredients may be contaminated with Salmonella.

    Product
    Cardboard sleeve: Cheese Club express mac Macaroni & Cheese Dinner, Four 2.05 OZ Bowls; Net Wt. 8.2 OZ.; Distributed by: Aldi, Inc., Batavia, IL 60510
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0988-2017·2017-01-18

    ICU Medical Recalls Tego Connectors Due to Potential Leaking Risk

    ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.

    Product
    Tego Connector, Item No. D1000, NM1000 The Tego¿ Needle Free Access Device is intended for use as an accessory to a vascular access device (catheter) used in Hemodialysis or as an accessory to an Intravascular Administration Set for the administration or withdrawal of fluids…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0868-2017·2017-01-18

    Koi Palace Mini Mooncakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Mooncakes due to missing ingredient labels and undeclared wheat, peanut oil, and egg yolk.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini White Lotus Seed Paste w/ Egg Yolk Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1224-2017·2017-01-18

    New Hope Mills Recalls Crepe Mix Due to Salmonella Risk

    New Hope Mills is recalling specific lots of Crepe Mix because the bulk milk powder used may be contaminated with Salmonella.

    Product
    NEW HOPE MILLS Crepe MIX, NET WT. 1 LB. 4 OZ, UPC 074703601529 --- 181 York Street, Auburn, New York 13021 ---Product is packaged in a brown paper bag
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0859-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes because they lack adequate labeling for undeclared allergens including wheat, gluten, eggs, milk, peanuts, pine nuts, almonds, walnuts, and sesame.

    Product
    Koi Palace Mini Moon Cake: 8 Mini Treasures Combo Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0963-2017·2017-01-18

    Stryker Recalls Reprocessed Ablation Catheter Cables Due to Sterility Concerns

    Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.

    Product
    Reprocessed Ablation Catheter Cable Catalog Number: CR3425CT, CR3434CT Ablation catheter cables are designed as electrode cables with a multi-pin connector on the distal end which connects to an ablation catheter and a multi-pin connector on the proximal end which connects…
    Category
    Medical Device
    Distribution
    35 states
  • HighFDA (Food)·F-1188-2017·2017-01-18

    Charles Chocolates Toffee Chocolate Macadamia Recalled for Hazelnut Mislabeling

    Charles Chocolates is recalling Toffee Chocolate Macadamia products due to a consumer complaint that the items contained hazelnuts instead of macadamia nuts.

    Product
    Charles Chocolates Toffee Chocolate Macadamia; NET WT. 6.2 oz .(180 grams) UPC: 8 59033 00440 6 Charles Chocolates, San Francisco, CA
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1248-2017·2017-01-18

    House-Autry Cheese Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Cheese Biscuit Mix because it contains milk from a supplier recalling product for possible Salmonella.

    Product
    House-Autry Cheese Biscuit Mix, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15510 8,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1005-2017·2017-01-18

    Philips Clinix RF Plus X-ray System Recalled for Tilt Hazard

    Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.

    Product
    FV-RF (Clinix RF Plus) Product Usage: A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V040000·2017-01-18

    Nissan Recalls 2015-2017 Altima Vehicles for Rear Door Latch Defect

    Nissan is recalling 2015-2017 Altima vehicles because improperly routed rear door latch cables may allow doors to open while driving, increasing injury risk.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1012-2017·2017-01-18

    Symmetry Surgical ULTRA Gravity Sterilizer Containers Recalled for Sealant Defect

    Symmetry Surgical is recalling 38 ULTRA Gravity sterilizer containers because deteriorated or missing base trim sealant could allow contaminants to enter the container.

    Product
    symmetry surgical ULTRA(R) Gravity container, REF numbers: C131310-G, C13134-G, C13135-G, C13136-G, C13139-G, C13854-G, C13855-G, C13856-G, C181310-G, C18134-G, C18135-G, C18136-G, C18138-G, C22854-G, C22855-G, C22856-G, C22858-G, C24134-G, C24135-G, C24136-G, C24138…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0953-2017·2017-01-18

    In2Bones Recalls NEOVIEW Locking Screws Due to Thread Dimensional Non-Conformity

    In2Bones is recalling 40 units of NEOVIEW locking screws due to dimensional non-conformity of the thread on the screw head. The recall covers units distributed in the US, France, and Switzerland.

    Product
    NEO SCREW 02.7-14MM LOCKING, REF W27 ST114, In2Bones, 28 chemin du petit bois, 69130 Ecully - France The NEOVIEW¿ Plating System is intended for fixation of intra-articular and extraarticular fractures of the distal radius and reconstruction of the distal radius
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1013-2017·2017-01-18

    Beckman Coulter Recalls UniCel DxH 800 Cellular Analysis System

    Beckman Coulter is recalling the UniCel DxH 800 Cellular Analysis System because it may fail to detect blasts in some blood samples.

    Product
    UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B68304
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0990-2017·2017-01-18

    Varian Eclipse Treatment Planning System Software Recall for Contouring Errors

    Varian Medical Systems is recalling 42 Eclipse Treatment Planning System devices due to a software defect that prevents contours from saving consistently.

    Product
    Eclipse Treatment Planning System version 13.MR2 [13.06.31 with Smart Segmentation Knowledge Based Contouring version 2.3 [2.3.12] Radiology: The Eclipse Treatment Planning System (Eclipse TPS) is used to plan radiotherapy treatments for patients with malignant or benign…
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1003-2017·2017-01-18

    Corvida Medical Recalls Halo Closed System Transfer Devices Due to Malfunction

    J&J Solutions, Inc. DBA Corvida Medical is recalling 5,520 Halo Closed System Transfer Devices because the needle does not retract. The devices were distributed in Maryland, Texas, and Wisconsin.

    Product
    Halo Closed System Transfer Device, closed syringe adaptor, REF CSA100, Rx only, Sterile, packaged as individual units, packed and shipped 60 units/box and 4 boxes/shipping carton Corvida Medical, Coralville, IA 52241.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Food)·F-1094-2017·2017-01-18

    Piazza Produce Garden Season No Salt Recalled for Undeclared Soybean Oil

    Piazza Produce is recalling Garden Season No Salt products because the labels do not list soybean oil as an ingredient.

    Product
    Garden season no salt, 5 lb plastic gallon, product number 63516; Garden season no salt, 1.25 lb plastic jar, product number 63514
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0869-2017·2017-01-18

    Koi Palace Mooncakes Recalled for Undeclared Allergens and Labeling Defects

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to inadequate labeling and undeclared allergens including wheat, walnut, pine nut, sesame, and egg yolk.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Fresh Five Nuts with Smoked Ham Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1246-2017·2017-01-18

    House Autry Corn Bread Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling House Autry Stone Ground Buttermilk Corn Bread Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House Autry, stone Ground Buttermilk Corn Bread Mix, Net wt. 8 oz. boxes, UPC Code 0 73484 15512 2,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0989-2017·2017-01-18

    Health Robotics Recalls i.v. Station Systems Due to Bag Mislabeling

    Health Robotics S.R.L. is recalling 121 i.v. Station and i.v. Station ONCO systems because a motor error caused misalignment and mislabeling of IV bags.

    Product
    i.v. Station and i.v. Station ONCO Automated Drug Compounding System, Pharmacy Compounding System Device Listing Number E454448
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1099-2017·2017-01-18

    Piazza Produce Recalls Italian Herb Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Italian Herb seasoning in various plastic containers because the product labeling does not list ingredients and contains undeclared soybean oil.

    Product
    Italian Herb seasoning, 6 lb plastic pail, product number 64688; Italian Herb seasoning, 1.5 lb plastic gallon, product number 64667; Italian Herb seasoning, 6 oz plastic jar, product number 64648; Italian Herb seasoning, 3 lb plastic pail, product number 64686
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1101-2017·2017-01-18

    Piazza Produce Lemon Pepper Recalled for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling specific Lemon Pepper products because the labels do not list ingredients, including undeclared soybean oil.

    Product
    Lemon Pepper, 5 lb plastic gallon, product number 65085; Lemon Pepper, 1.25 lb plastic jar, product number 65066; Lemon Pepper, 12 lb plastic pail, product number 65104
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0951-2017·2017-01-18

    Natus Warmette Blanket and Dual Cabinets Recalled for Fuse Failure

    Natus Manufacturing Limited is recalling 31 Warmette Blanket and Dual Cabinets because a fuse may blow, causing power loss and potential melting of the fuse cover.

    Product
    Natus Warmette Blanket Cabinet and Warmette Dual Cabinet The Natus Warmette Blanket Cabinet is designed to store and warm blankets and hospital linens; while, the Natus Warmette Dual Cabinet is designed to store and warm blankets and hospital linens in one compartment and…
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Food)·F-0860-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient and allergen labels. The product contains undeclared wheat, walnuts, and pine nuts.

    Product
    Koi Palace Mini Moon Cake: Five Nuts with Smoked Ham & Egg Yolk Unit Size 1/2 lb. and 1/4 lb. in circular box (1 piece) and rectangular boxes (4, 6 or 8 pieces).
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1109-2017·2017-01-18

    Piazza Produce Salt Free Vegetable Herb Recalled for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Salt Free Vegetable Herb products because the labels do not list ingredients, including undeclared soybean oil.

    Product
    Salt Free Vegetable Herb, 5.5 lb plastic gallon, product number 63524; Salt Free Vegetable Herb, 1.5 lb plastic jar, product number 63522
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0956-2017·2017-01-18

    Zimmer Biomet Recalls Oxford Fixed Lateral Bearings Due to Mislabeling

    Zimmer Biomet is removing a specific lot of Oxford Fixed Lateral Bearings because packages labeled as 'Right' contained 'Left' bearings.

    Product
    Oxford Fixed Lateral Bearing Size F Right, Part Number 154375 Lot 744260, Sterile, The product is placed into an Aluminum Oxide coated PET pouch and vacuum sealed with an Argon flush. The vacuum sealed part is then placed into a coated 1073B Tyvek/film pouch and heat sealed.…
    Category
    Medical Device
    Distribution
    0 states