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.

33376–33400 of 50502

  • HighFDA (Food)·F-0867-2017·2017-01-18

    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 allergens including wheat, peanut oil, and coconut.

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Bird's Nest, Black Sesame & Coconut Paste 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-1105-2017·2017-01-18

    Piazza Produce Recalls Quebec Steak Seasoning for Undeclared Soybean Oil

    Piazza Produce, Inc. is recalling Quebec Steak seasoning in three sizes because the product labeling does not list ingredients and contains undeclared soybean oil.

    Product
    Quebec Steak seasoning, 1.5 lb plastic jar, product number 67783; Quebec Steak seasoning, 6 lb plastic gallon, product number 67802; Quebec Steak seasoning, 10 lb plastic pail, product number 67821
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-0862-2017·2017-01-18

    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 and contain undeclared allergens.

    Product
    Koi Palace Mini Moon Cake: Dalmaji with Happy Family 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-0858-2017·2017-01-18

    Koi Palace Mini Moon Cakes Recalled for Undeclared Allergens

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

    Product
    Koi Palace Mini Moon Cake: 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-0877-2017·2017-01-18

    Capitol City Specialties Recalls Peanut Butter Jars for Undeclared Soy Lecithin

    Capitol City Specialties Company is recalling 900 jars of Dashing Thru the Dough Gourmet Chocolate Chip Cookie Dough Peanut Butter due to undeclared soy lecithin.

    Product
    the Peanut Principle, Dashing Thru the Dough, Gourmet Chocolate Chip Cookie Dough Peanut Butter, NET WT 16oz, UPC 609207898788
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0962-2017·2017-01-18

    Medtronic MRI-Conditional Cardiac Devices Recalled for Software Feature Error

    Medtronic is recalling 21,111 MRI-conditional cardiac resynchronization therapy devices because the AdaptivCRT feature may appear enabled when it is not active.

    Product
    Amplia MRI" CRT -D SureScan", Amplia MRI" Quad CRT -D SureScan", Claria MRI" CRT -D SureScan", Claria MRI" Quad CRT -D SureScan. implantable medical devices that automatically detect and treat episodes of ventricular fibrillation, ventricular tachycardia, fast ventricular…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1252-2017·2017-01-18

    Roy Roger's Pancake Mix Recalled for Possible Salmonella Contamination

    House-Autry Mills is recalling Roy Roger's Pancake Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Roy Roger's Pancake Mix, Net Wt., 2 lb. 8 oz. bags, UPC Code 0 73484 22724 0
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-0870-2017·2017-01-18

    Koi Palace Mini Mooncakes Recalled for Undeclared Wheat and Peanut Oil

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

    Product
    Koi Palace Mini Moon Cake: Luxury Single Mooncake - Mini Fresh Jasmine Paste. 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-0967-2017·2017-01-18

    C.R. Bard Recalls Medical Devices Containing Latex Catheters

    C.R. Bard is recalling specific medical device trays and stabilization devices because they contained latex catheters instead of silicone catheters.

    Product
    SURESTEP Tray, BARDEX I.C. COMPLETE CARE, Urine Meter, Temperature STATLOCK Stabilization Device
    Category
    Medical Device
    Distribution
    23 states
  • HighFDA (Devices)·Z-1011-2017·2017-01-18

    Symmetry Surgical ULTRA Sterrad Container Recall for Sealant Defect

    Symmetry Surgical is recalling 149 ULTRA Sterrad containers because deteriorated or missing base trim sealant may allow contaminants to enter the container after sterilization.

    Product
    symmetry surgical ULTRA(R) Sterrad container, REF numbers: C131310-SP, C13134-SP, C13135-SP, C13136-SP, C13139-SP, C13854-SP, C13855-SP, C13856-SP, C181310-SP, C18134-SP, C18135-SP, C18136-SP, C18138-SP, C22854-SP, C22855-SP, C22856-SP, C22858-SP, C24134-SP, C24135-SP…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1223-2017·2017-01-18

    Portland Specialty Baking Recalls White Cake Due to Undeclared Walnut

    Portland Specialty Baking LLC is recalling ALN UNICED 1/4 Sheet Split Layer White Cake because it may contain walnut, which is not listed on the label.

    Product
    ALN UNICED 1/4 Sheet Split Layer White Cake, Item 00886, three stacked cake layers with plastic liner in between layers are packaged in a corrugated box, a total of 12 cakes per bulk box. UPC 00750903008862
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1006-2017·2017-01-18

    Philips IQon Spectral CT Recalled for Image and Scan Errors

    Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.

    Product
    IQon Spectral CT with software version 4.7.0 Product Usage: The IQon Spectral CT is a Computed Tomography X-Ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. This…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1225-2017·2017-01-18

    Brand Castle Monkey Bread Mix Recalled for Salmonella

    Brand Castle LLC is recalling In The Mix Monkey Bread Mix because the facility and finished product tested positive for Salmonella.

    Product
    In The Mix¿ Monkey Bread Mix NET WT 16 oz (16 lb) 454 g box, INGREDIENTS: BREAD MIX: ***BUTTERMILK*** DISTRIBUTED BY BRAND CASTLE, LLC BEDFORD HTS, OH 44146 www.brandcastle.com UPC 8 44527 03278 2
    Category
    Food
    Distribution
    38 states
  • HighFDA (Food)·F-1217-2017·2017-01-18

    Stonewall Kitchen Cinnamon Apple Pancake Mix Recalled for Salmonella Risk

    Stonewall Kitchen is recalling Cinnamon Apple Pancake & Waffle Mix due to potential Salmonella contamination. Consumers should stop using the product.

    Product
    Stonewall Kitchen Cinnamon Apple Pancake & Waffle Mix, 16 oz. canister UPC: 711381025659 Item #: 551118
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0865-2017·2017-01-18

    Koi Palace Mini Moon Cake Recalled for Undeclared Wheat and Peanut Oil

    Magic Gourmet Trading Inc. is recalling Koi Palace Mini Moon Cakes due to missing ingredient statements and undeclared wheat and peanut oil.

    Product
    Koi Palace Mini Moon Cake: Single Box - Mini Oolong Tea Paste 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-1247-2017·2017-01-18

    House-Autry Buttermilk Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buttermilk Biscuit Mix because it contains milk from a supplier recalling product due to possible Salmonella.

    Product
    House-Autry Buttermilk Biscuit Mix Tote, Net Wt., 8 oz. (227 g.), UPC Code 0 73484 15500 9,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-1007-2017·2017-01-18

    Medtronic Recalls AxIEM Touch N Go Pointer Probe for Accuracy Issues

    Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.

    Product
    AxIEM Touch N Go Pointer Probe. Model Number: 9735318. Placed in a 30mil PETG tray sealed with a Tyvek lid and then placed in a shelf carton.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0861-2017·2017-01-18

    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 and contain undeclared allergens.

    Product
    Koi Palace Mini Moon Cake: Seven Stars Reunion 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-0866-2017·2017-01-18

    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 for wheat, peanut oil, and walnuts.

    Product
    Koi Palace Mini Moon Cake: Single Box - Mini Walnut, Red Bean Paste 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-1010-2017·2017-01-18

    Symmetry Surgical ULTRA Steam Container Recall for Sealant Defect

    Symmetry Surgical is recalling ULTRA Steam containers because deteriorated or missing base trim sealant may allow contaminants to enter after sterilization.

    Product
    symmetry surgical ULTRA(R) Steam container, REF numbers: C131310, C13134, C13135, C13136, C13139, C13854, C13855, C13856, C181310, C18134, C18135, C18136, C18138, C22854, C22855, C22856, C22858, C24134, C24135, C24136 Product Usage: sterilization container
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1249-2017·2017-01-18

    House-Autry Butterflake Biscuit Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling 606 bags of Butterflake Biscuit Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    House-Autry Butterflake Biscuit Mix, Net Wt. 25 lb. bags, UPC Code 0 73484 20513 1,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Food)·F-1250-2017·2017-01-18

    Buddy's Bar-B-Q Hushpuppy Mix Recalled for Possible Salmonella

    House-Autry Mills is recalling Buddy's Bar-B-Q Hushpuppy Mix because it contains milk product from a supplier recalling for possible Salmonella.

    Product
    Buddy's Bar-B-Q Hushpuppy Mix, Net Wt., 5 lb bags, UPC Code 0 73484 22156 2,
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0966-2017·2017-01-18

    Amendia Recalls Ceres-C Cervical Interbody Devices Due to Missing Pin

    Amendia, Inc. is recalling six Ceres-C Standalone Cervical Interbody devices because they are missing a tantalum market pin.

    Product
    Ceres-C Standalone Cervical Interbody The product is a stand-alone anterior cervical interbody fusion device indicated for use in skeletally mature patients with degenerative disc disease (DDD) with accompanying radicular symptoms at the one level from C2-T1.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0972-2017·2017-01-18

    Siemens Recalls Artis Q Angiographic X-Ray Systems for Generator Defects

    Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.

    Product
    Artis Q/Q.zen, Angiographic x-ray system Stand alone system The Artis systems are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide