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.

25476–25500 of 50447

  • HighFDA (Devices)·Z-1859-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk

    Maquet is recalling 12 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229002A Model: VST66SF AIM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1855-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled Due to Coating Crack Risk

    Maquet is recalling 46 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, risking particle contamination in the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811961 Model: VLT600DF AIM STP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1498-2019·2019-07-03

    Hank's Cheesecakes Recalls Turtle Cheesecakes Lacking Allergen Labels

    Hank's Cheesecakes, LLC is recalling 207 Turtle Cheesecakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    Turtle Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1512-2019·2019-07-03

    Hank's Tiramisu Cheesecake Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling Tiramisu Cheesecakes because the packaging lacks ingredient and major food allergen information.

    Product
    Tiramisu Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1510-2019·2019-07-03

    Hank's Cheesecakes Recalls Chocolate Raspberry Cakes for Missing Allergen Labels

    Hank's Cheesecakes, LLC is recalling 207 chocolate raspberry cakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    Chocolate Raspberry Cake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1507-2019·2019-07-03

    Hank's Blueberry Cheesecakes Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling 207 blueberry cheesecakes because they lack labels indicating ingredients and major food allergens.

    Product
    Blueberry Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1493-2019·2019-07-03

    Hank's Cheesecakes Recalled for Missing Allergen and Ingredient Labels

    Hank's Cheesecakes, LLC is recalling plain cheesecakes distributed in Missouri and Illinois because the packages lack labels indicating ingredients or major food allergens.

    Product
    Plain Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1506-2019·2019-07-03

    Hank's Banana Cheesecake Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling 207 banana cheesecakes because they lack labels indicating ingredients and major food allergens.

    Product
    Banana Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1886-2019·2019-07-03

    GE Healthcare Recalls Centricity Universal Viewer for Missing Image Warning

    GE Healthcare is recalling 292 units of the Centricity Universal Viewer because it may fail to warn users when medical images are missing from exams.

    Product
    Centricity Universal Viewer with PACS-IW foundation 6.0, Model number 2090255-001 Product Usage: Centricity PACS-IW with Universal Viewer is a device that displays medical images (including mammograms) and data from various imaging sources. Images and data can be viewed…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V512000·2019-07-03

    Winnebago Forza Motorhomes Recalled for Storage Door Defect

    Winnebago is recalling 2017-2019 Forza motorhomes because the exterior storage compartment door may unexpectedly open while driving, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO FORZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1863-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk

    Maquet is recalling 9 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, posing a risk of particles falling into the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229036A Model:VST66SF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1856-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk

    Maquet is recalling 7 units of VOLISTA StandOP Surgical Lights because the coating on the light head forks may crack, posing a risk of particles falling into the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568812910 Model: VLT400SF STP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1876-2019·2019-07-03

    GE Healthcare Recalls ECG Leadwire Sets Due to Defibrillation Risk

    GE Healthcare is recalling ECG leadwire sets because they may reduce energy reaching patients during defibrillation, potentially limiting treatment success.

    Product
    ECG leadwire sets: REF/Catalog Number Description 2106389-001 ECG Leadwire set, 5-lead, grouped, grabber, AHA, 74 cm/ 29 in 2106389-002 ECG Leadwire set, 5-lead, grouped, grabber, AHA, 130 cm/ 51 in 2106389-003 ECG Leadwire set, 5-lead, grouped, grabber, IEC, 74 cm/ 29 in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1872-2019·2019-07-03

    Thermo Scientific General Purpose Dynamic Bath Recalled for Assembly Error

    Thermo Fisher Scientific is recalling three General Purpose Dynamic Bath units due to an assembly error that may cause the fluid temperature to rise above the user's set point.

    Product
    Thermo Scientific General Purpose Dynamic Bath Precision 28L GP Bath Model Number: TSGP28
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-1511-2019·2019-07-03

    Hank's Chocolate Swirl Cheesecake Recalled for Missing Allergen Labels

    Hank's Cheesecakes, LLC is recalling 207 Chocolate Swirl Cheesecakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    Chocolate Swirl Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1877-2019·2019-07-03

    GE Healthcare Recalls ECG Leadwires Due to Defibrillation Energy Reduction

    GE Healthcare is recalling 58,045 replacement ECG leadwires because they may reduce energy reaching patients during defibrillation, potentially limiting treatment success.

    Product
    Replacement leadwires with grabber ends: REF/Catalog Number Description 2106388-005 Replacement ECG Leadwire, grabber, BRN V, AHA, 74 cm/ 29 in 2106388-101 Replacement ECG Leadwire, grabber, LL , AHA, 130 cm/ 51 in 2106388-103 Replacement ECG Leadwire, grabber, GRN RL, AHA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1502-2019·2019-07-03

    Hank's Caramel Macchiato Cheesecakes Recalled for Missing Allergen Labels

    Hank's Cheesecakes is recalling Caramel Macchiato Cheesecakes because they lack labels indicating ingredients and major food allergens.

    Product
    Caramel Macchiato Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1854-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled Due to Coating Crack Risk

    Maquet is recalling 65 VOLISTA StandOP Surgical Lights because the coating on the light head forks may crack, posing a risk of particles falling into the surgical field and causing patient infection.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARD568811911 Model: VLT600SF AIM STP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1497-2019·2019-07-03

    Hank's Cheesecakes Recalls Chocolate Cakes Lacking Allergen Labels

    Hank's Cheesecakes, LLC is recalling 207 chocolate cakes because they were distributed without labels indicating ingredients or major food allergens.

    Product
    Chocolate Cake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1871-2019·2019-07-03

    Thermo Scientific Dual GP Bath Recalled for Assembly Error

    Thermo Fisher Scientific is recalling four Thermo Scientific General Purpose Dynamic Bath units due to an assembly error that may cause the fluid temperature to rise above the set point.

    Product
    Thermo Scientific General Purpose Dynamic Bath Precision 5 & 10L Dual GP Bath Model Number: TSGP15D
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1864-2019·2019-07-03

    Maquet VOLISTA Surgical Lights Recalled for Coating Crack Risk

    Maquet is recalling 10 VOLISTA StandOP Surgical Lights because light head fork coatings may crack, potentially dropping particles into the surgical field.

    Product
    Maquet VOLISTA StandOP Surgical Lights- Product Code: ARDVST229037A Model: VST66DF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1499-2019·2019-07-03

    Hank's Cheesecake Strawberry Cheesecake Recalled for Missing Allergen Labels

    Hank's Cheesecakes, LLC is recalling 207 Strawberry Cheesecakes distributed in Missouri and Illinois because they lack labels indicating ingredients and major food allergens.

    Product
    Strawberry Cheesecake in a cardboard box labeled Hank's Cheesecake, St. Louis Missouri 63117
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1865-2019·2019-07-03

    Thermo Fisher Water Bath Recall Due to Assembly Error

    Thermo Fisher Scientific is recalling 10 Fisher Scientific Isotemp water baths because an assembly error may cause the fluid temperature to rise above the user's set point.

    Product
    Fisher Scientific Isotemp -General Purpose Water Bath: lsotemp 5L GP Bath Model Number: FSGPD05
    Category
    Medical Device
    Distribution
    4 states