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.

45251–45275 of 50512

  • HighFDA (Food)·F-1821-2012·2012-08-08

    Spillson's Ham Sandwiches Recalled for Undeclared Wheat and Soy Allergens

    Spillson's Ltd. is recalling 42 units of 7-ounce ham sandwiches due to undeclared wheat and soy ingredients. Consumers with allergies to wheat or soy should not consume the product.

    Product
    Spillson's Ltd. Ham Sandwich Nt. Wt. 7 oz
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2106-2012·2012-08-08

    Intuitive Surgical Recalls Instrument Arm Drapes Due to Adaptor Engagement Issues

    Intuitive Surgical is recalling specific lots of Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument during surgery.

    Product
    ACCESSORY BASE STARTER KIT,IS3000; Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vinci Surgical Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0859-2012·2012-08-08

    Arm and Hammer Spinbrush Recall for Choking Hazard

    Church & Dwight is recalling Spinbrush Pro Whitening toothbrushes due to a potential small parts choking hazard if used beyond the recommended 3-month brush head life.

    Product
    Arm and Hammer Spinbrush Dual Action Powered Toothbrush Spinbrush Pro Whitening Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2095-2012·2012-08-08

    Church & Dwight Recalls Spinbrush Pro White Sonic Crest Toothbrushes

    Church & Dwight is recalling Spinbrush Pro White Sonic Crest Powered Toothbrushes due to a potential small parts choking hazard if used beyond the recommended 3-month brush head life.

    Product
    Arm and Hammer Spinbrush Pro White Sonic Crest Powered Toothbrush Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2102-2012·2012-08-08

    Intuitive Surgical Recalls Specific Lots of da Vinci Instrument Arm Drapes

    Intuitive Surgical is recalling specific lots of da Vinci Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument.

    Product
    KIT,DISPOSABLE ACCESSORY,3ARM,IS2000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vinci Surgical Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2094-2012·2012-08-08

    Arm and Hammer Spinbrush Pro Clean Sonic Toothbrush Recall for Choking Hazard

    Church & Dwight is recalling Arm and Hammer Spinbrush Pro Clean Sonic toothbrushes due to a small parts choking hazard if brush heads are used beyond their recommended life.

    Product
    Arm and Hammer Spinbrush Pro Clean Sonic Color Wear Powered Toothbrush Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2123-2012·2012-08-08

    Integra Advansys Medial Lisfranc Plate Recalled for Surgical Technique Risk

    Integra LifeSciences is recalling Advansys Medial Lisfranc Plates because an incorrect surgical technique may cause potential rupture of the tibialis anterior tendon.

    Product
    Integra¿ Advansys Medial Lisfranc Plate (MLP), Integra, 311 Enterprise Drive, Plainsboro, NJ 08536 The Advansys plates are intended for bone fixation such as: Arthrodesis of the 1st metatarsocuneiform joint to reposition and stabilize a metatarsus primus varus, Lisfranc…
    Category
    Medical Device
    Distribution
    40 states
  • HighFDA (Devices)·Z-2099-2012·2012-08-08

    Arm and Hammer Spinbrush ProClean Sonic Recharge Recalled for Choking Hazard

    Church & Dwight is recalling Arm and Hammer Spinbrush ProClean Sonic Recharge units due to a potential choking hazard from small parts if used beyond the recommended brush head life.

    Product
    Arm and Hammer Spinbrush ProClean Sonic Recharge Color Wear Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2134-2012·2012-08-08

    Stryker Recalls 210 RF Cannula Units Due to Packaging Error

    Stryker is recalling 210 RF Cannula units because 5mm and 10mm needles were mistakenly packaged in the wrong boxes. This error could lead to thermal skin lesions if the larger tip is used in cervical procedures.

    Product
    RF Cannula, 100 mm,Curved 5 MM, 20 G, REF 0406-630-115 RX only, Disposable ( 10/pk) Product Usage: The Stryker RF Cannulae, in combination with the Stryker RF Generator/Multi- Gen and electrodes, are intended for coagulation of soft tissue in orthopedic, arthroscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2121-2012·2012-08-08

    Perkin Elmer Genetic Screening Processor Recalled for Shaker Unit Contamination

    Perkinelmer is recalling 78 Genetic Screening Processor units worldwide because shaker unit contamination causes decreased signal activity in neonatal screening assays.

    Product
    Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Product Usage: The GSP instrument is a fully automated, high throughput batch analyzer for time- resolved and prompt fluorescence analysis of samples in microtitration plates. It is intended for in vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1831-2012·2012-08-08

    Spillson's Pizza Boat Recalled for Undeclared Wheat Allergen

    Spillson's Ltd. is recalling 4 oz. Pizza Boats because they contain undeclared wheat. People with wheat allergies or sensitivities are at risk of serious reactions.

    Product
    Spillson's Ltd. Pizza Boat, 4 oz.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2096-2012·2012-08-08

    Arm and Hammer Spinbrush Pro White Sonic Toothbrush Recalled for Choking Hazard

    Church & Dwight is recalling Arm and Hammer Spinbrush Pro White Sonic Toothbrushes due to a potential choking hazard from small parts if used beyond the recommended 3-month brush head life.

    Product
    Arm and Hammer Spinbrush Pro White Sonic Toothbrush Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2108-2012·2012-08-08

    Maquet Magnus Carbon-Fibre Operating Table Top Recall for Brake Defect

    Maquet is recalling specific Magnus carbon-fibre operating table tops due to a potential issue with motor brakes for the longitudinal shift and tilt drives.

    Product
    Maquet Getinge Group Operating Table System Magnus Carbon-Fibre Table Top Version 1180.16 The carbon-fibre MAGNUS table top (1180-16XX) serves to support and position patients for surgical procedures (e.g. cardiovascular surgery) and interventional examination immediately…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2097-2012·2012-08-08

    Arm and Hammer Spinbrush Pro Clean Sonic Tray Recalled for Choking Hazard

    Church & Dwight is recalling Arm and Hammer Spinbrush Pro Clean Sonic Trays due to a potential small parts choking hazard if used beyond the recommended 3-month brush head life.

    Product
    Arm and Hammer Spinbrush Pro Clean Sonic Tray BJS Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Food)·F-1841-2012·2012-08-08

    Cafe Moto Almond Truffle Coffee Recalled for Undeclared Milk

    Cafe Moto is recalling Almond Truffle Flavored Coffee because the flavoring contains whey, a milk derivative, which is not declared on the label.

    Product
    Flavored coffee. Cafe Moto Almond Truffle Flavored Coffee, 16 oz.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1834-2012·2012-08-08

    Spillson's Breakfast Muffin Sandwich Recalled for Undeclared Wheat and Soy

    Spillson's Ltd. is recalling Breakfast Muffin Sandwiches containing undeclared wheat and soy lecithin. People with allergies to these ingredients are at risk of serious reactions.

    Product
    Spillson's Ltd. Breakfast Muffin Sandwich, 6 oz Ham
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2098-2012·2012-08-08

    Arm and Hammer Spinbrush Pro Clean Sonic Recharge Recalled for Choking Hazard

    Church & Dwight is recalling Arm and Hammer Spinbrush Pro Clean Sonic Recharge units due to a potential small parts choking hazard when used beyond the recommended brush head life.

    Product
    Arm and Hammer Spinbrush Pro Clean Sonic Recharge Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-0858-2012·2012-08-08

    Arm and Hammer Spinbrush Toothbrush Recalled for Choking Hazard

    Church & Dwight is recalling Arm and Hammer Spinbrush toothbrushes due to a potential choking hazard from small parts if used beyond the recommended brush head life.

    Product
    Arm and Hammer Spinbrush Dual Action Powered Toothbrush Pro Clean Re-Charge Made in China. Manufactured for Church and Dwight Co., Inc. Princeton, NJ 08543 USA. For dental health; plaque removal.
    Category
    Consumer Product
    Distribution
    0 states
  • HighFDA (Devices)·Z-2126-2012·2012-08-08

    GE OEC Medical Systems Recalls Mobile C-Arm Devices for Hard Disk Drive Issue

    GE OEC Medical Systems is recalling OEC MiniView 6800 Mobile C-Arms due to a hard disk drive issue. The recall covers 82 units distributed worldwide.

    Product
    OEC MiniView 6800 Mobile; MDL number A349855. Product Usage: The mini 6800 digital mobile c arm is designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical, orthopedic, and extremity imaging. The device…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2104-2012·2012-08-08

    Intuitive Surgical Recalls Specific Lots of da Vinci Instrument Arm Drapes

    Intuitive Surgical is recalling specific lots of da Vinci Instrument Arm Drapes because the sterile adaptor may have difficulty engaging an instrument.

    Product
    KIT,DISPOSABLE ACCESSORY,3ARM,IS3000,5 PACK; Product Usage: The intended use of the Instrument arm drape is to protect equipment from contamination and to maintain a sterile field during surgical procedures using the da Vinci Surgical Systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1833-2012·2012-08-08

    Spillson's Double Cheeseburger Sandwich Recalled for Undeclared Soy Lecithin

    Spillson's, Ltd. is recalling Double Cheeseburger Sandwiches because they contain undeclared soy lecithin. The source text notes a risk of serious reaction for people with wheat allergies.

    Product
    Spillson's Ltd. Double Cheeseburger Sandwich.
    Category
    Food
    Distribution
    1 state