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.

45151–45175 of 50512

  • HighFDA (Food)·F-1954-2012·2012-08-29

    Flywheel's Pies Recalls Cherry Pies Due to Undeclared Allergens

    Flywheel's Pies is recalling cherry pies sold in Arkansas because they contain undeclared soy lecithin, soybean oil, and wheat.

    Product
    Cherry Pies Case Label (side 1) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Cocoa, Coconut, Sugar, Butter, Vanilla, Cornstarch, Eggs Case Label (side 2) 24 COUNT FRAGILE, FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Fruit, Sugar, Butter, Almond, Salt Pie…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1952-2012·2012-08-29

    Flywheel's Pies Recalls Apple Pies for Undeclared Allergens

    Flywheel's Pies is recalling apple pies sold in Arkansas due to undeclared soy lecithin, partially hydrogenated soybean oil, and wheat.

    Product
    Apple Pies Case Label (side 1) 24 COUNT FRAGILE FLYWHEEL'S PIES, PRESCOTT, AR Ingredients: Cocoa, Coconut, Sugar, Butter, Vanilla, Cornstarch, Eggs Case Label (side 2) 24 COUNT FRAGILE FLYWHEEL'S PIES PRESCOTT, AR Ingredients: Fruit, Sugar, Butter, Almond, Salt. Pie…
    Category
    Food
    Distribution
    1 state
  • HighCPSC·12257·2012-08-28

    Eecycleworks Recalls Bicycle Brakes Due to Fall Hazard

    Eecycleworks is recalling about 400 'eebrake' model bicycle brakes because the bridge can crack, posing a fall hazard to riders.

    Product
    Bicycle brakes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12260·2012-08-28

    Sherwin-Williams Recalls Tree House Acrylic Coating Due to Fire Hazard

    Sherwin-Williams is recalling Tree House Studio Clear Acrylic Matte Coating because the aerosol canister can leak, posing a fire hazard if stored near ignition sources.

    Product
    Tree House Studio™ Clear Acrylic Matte Coating
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12255·2012-08-23

    Zest Garden Recalls Wilson & Fisher Bistro Sets Due to Fall Hazard

    Zest Garden is recalling Wilson & Fisher White Cast Bistro Sets because the chairs can break during normal use, posing a fall hazard.

    Product
    Wilson & Fisher White Cast Bistro Table and Chairs Set
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12746·2012-08-23

    Mansfield Plumbing Recalls Acrylic Bathtubs and Whirlpools Due to Fall Hazard

    Mansfield Plumbing Products is recalling about 100 acrylic bathtubs, whirlpools, and air massage bathtubs because the grab bars can loosen and break, posing a fall hazard.

    Product
    Acrylic Bathtubs, Whirlpools and Air Massage Bathtubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2190-2012·2012-08-22

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues

    Edwards Lifesciences is recalling Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.

    Product
    Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HF7J. For use in patients who require hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1943-2012·2012-08-22

    Baroody Imports Recalls Chiclets Chewing Gum for Unsafe Color Additives

    Baroody Imports Inc. is voluntarily recalling Chiclets Chewing Gum (Fruit Flavors) due to misbranded and unsafe color additives.

    Product
    Chiclets Chewing Gum Fruit Flavors; Made in Lebanon; Manufactured by Cadbury Adams Middle East S.A.L.
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-2203-2012·2012-08-22

    GE Healthcare Advantage Workstations Recalled for Incorrect Aorta Measurements

    GE Healthcare is recalling Advantage Workstations with Advanced Vessel Analysis due to incorrect aorta measurements and potential issues with PET data loading.

    Product
    GE Healthcare Advantage Workstations, Advantage Worksation version 4.2 and 4.3 with Volume Viewer 2 (version 6.4-6.8) provided with Advance Vessel Analysis (AVA) and Advantage Workstation 4.4 with Volume Viewer 2 (version 6.8 or before) or Volume Viewer 3 (version 7.2 -7.3)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1937-2012·2012-08-22

    Icrest International Recalls Frozen Oyster Meat Due to Insanitary Conditions

    Icrest International LLC is recalling frozen oyster meat from Korea because it was prepared under insanitary conditions, potentially rendering it injurious to health.

    Product
    OYSTER MEAT IQF TINY 40/8OZ PRODUCT OF KOREA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2194-2012·2012-08-22

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues

    Edwards Lifesciences is recalling 32,145 units of Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.

    Product
    Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 141HF7J. For use in patients who require hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2192-2012·2012-08-22

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues

    Edwards Lifesciences is recalling 32,145 Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.

    Product
    Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131HVF7P. For use in patients who require hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1932-2012·2012-08-22

    Southern Home Pasta Salad Recalled for Potential Metal Fragments

    Southern Home is recalling specific lots of Pasta Salad Ranch with Bacon because they may contain metal fragments.

    Product
    Southern Home Pasta Salad Ranch with Bacon, 7.5 oz., UPC 0788002891, 12 packages per case
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2212-2012·2012-08-22

    Zimmer Recalls Trabecular Metal Reverse Shoulder Liner Impactors

    Zimmer, Inc. is recalling Trabecular Metal Reverse Shoulder Liner Impactors due to reports of alignment peg fractures in units made of 455 stainless steel.

    Product
    Trabecular Metal Reverse Shoulder Liner 40mm, part 00-4309-028-00 - Per surgical technique 97-4309-003-00 Revision 4: "Complete Poly Liner insertion by snapping the appropriate 60¿ (Standard) or 65¿ (Retentive) Poly Liner Impactor to the Poly Liner Impactor Handle. Then…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2214-2012·2012-08-22

    Zimmer Recalls Trabecular Metal Reverse Shoulder Liner Impactors

    Zimmer, Inc. is recalling specific Trabecular Metal Reverse Shoulder Liner Impactors due to reports of alignment peg fractures.

    Product
    00-4309-029-00- Trabecular Metal Reverse Shoulder Liner 36mm, Nonsterile Per surgical technique 97-4309-003-00 Revision 4: "Complete Poly Liner insertion by snapping the appropriate 60¿ (Standard) or 65¿ (Retentive) Poly Liner Impactor to the Poly Liner Impactor Handle. Then…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2213-2012·2012-08-22

    Zimmer Trabecular Metal Reverse Shoulder Liner Impactors Recalled for Fractures

    Zimmer, Inc. is recalling Trabecular Metal Reverse Shoulder Liner Impactors due to reports of alignment peg fractures in instruments made of 455 stainless steel.

    Product
    00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck Angle Per surgical technique 97-4309-003-00 Revision 4: "Complete Poly Liner insertion by snapping the appropriate 60¿ (Standard) or 65¿ (Retentive) Poly Liner Impactor to the Poly Liner Impactor Handle.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2196-2012·2012-08-22

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues

    Edwards Lifesciences is recalling Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.

    Product
    Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151F7. For use in patients who require hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2193-2012·2012-08-22

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues

    Edwards Lifesciences is recalling Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.

    Product
    Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 141F7. For use in patients who require hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2189-2012·2012-08-22

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues

    Edwards Lifesciences is recalling Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.

    Product
    Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 131F7P. For use in patients who require hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2197-2012·2012-08-22

    Edwards Lifesciences Recalls Swan-Ganz Catheters Due to Guidewire Passage Issues

    Edwards Lifesciences is recalling 32,145 Swan-Ganz Thermodilution VIP Catheters because a J-tip guidewire may pass through the distal lumen hub.

    Product
    Edwards Lifesciences Swan-Ganz Thermodilution VIP Catheters Model 151HF7. For use in patients who require hemodynamic monitoring.
    Category
    Medical Device
    Distribution
    Distributed nationwide