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.

32326–32350 of 50502

  • HighNHTSA·17V317000·2017-05-11

    Thomas Built Buses Recalls 2013-2018 Saf-T-Liner HDX School Buses

    Daimler Trucks North America is recalling 2013-2018 Thomas Built Saf-T-Liner HDX school buses because seat lap belts may be anchored to the seat rather than the bus structure.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1924-2017·2017-05-10

    Natus Medical Recalls neoBLUE 2 Phototherapy Lights for Intensity Defect

    Natus Medical is recalling neoBLUE 2 phototherapy lights sold from 2003 to 2008 to prevent the use of replacement boards that allow higher light intensity than originally cleared.

    Product
    Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between 2003 and 2008. Catalog Part Number 010066. Top Assembly Part Numbers: 040906, 040904, 040756, 040758, 040658, 040680. Product Usage: Device is used to provide treatment for neonatal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17E025000·2017-05-10

    Sprague Heavy-Duty Bus Wiper Arms Recalled for Mounting Casting Cracks

    Sprague Devices is recalling Heavy-Duty Bus Pantograph Wiper Arms because the mounting casting may crack, causing the arms to bend or detach and reducing driver visibility.

    Product
    VISIBILITY:WINDSHIELD WIPER/WASHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1928-2017·2017-05-10

    Dale Medical Stabilock Endotracheal Adhesive Base Recalled for Adhesive Failure

    Dale Medical Products is recalling Stabilock Endotracheal Adhesive Bases because the adhesive faceplate may lose its properties and fail to adhere to the patient's face.

    Product
    Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of an adhesive base, Dale product number 273, that attaches to the patient's skin and a cushioned neckband with tube channel that…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2161-2017·2017-05-10

    Goya Octopus in Garlic Sauce Recalled for Squid Mislabeling

    Tradewind Foods is recalling Goya Octopus in Garlic Sauce because the product contains squid instead of octopus. This mislabeling poses a risk to consumers with seafood allergies.

    Product
    Goya Octopus in Garlic Sauce, Pulpo al Ajillo, NET WT./PESO NETO 4 oz. (113g), PRODUCT OF SPAIN "WILD FISH", GOYA FOODS, INC., Secaucus N.J. 07096.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1890-2017·2017-05-10

    Medtronic Recalls MiniMed 620G and 640G Insulin Pumps Due to Software Anomaly

    Medtronic is recalling MiniMed 620G and 640G insulin pumps with software version 2.6 or below because a software anomaly can prevent the internal battery from charging, leading to pump shutdown.

    Product
    MiniMed 620G and MiniMed 640G Insulin Pumps with Software Version 2.6 and below are affected. Catalog Numbers for these insulin pumps are MMT-1510, MMT-1710, MMT-1711, MMT-1712.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1903-2017·2017-05-10

    Breg Inc Recalls Sterile Dressings Due to Unsealed Pouches

    Breg Inc is recalling 2,609 units of Dressing Rect L (P/N 02428) because some may have unsealed pouches, rendering them non-sterile.

    Product
    Dressing Rect L, P/N 02428 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2163-2017·2017-05-10

    Goya Octopus in Hot Sauce Recalled for Squid Mislabeling

    Tradewind Foods is recalling Goya Octopus in Hot Sauce because the product contains squid instead of octopus, posing a risk to consumers with octopus allergies.

    Product
    Goya Octopus in Hot Sauce, Pulpo en Salsa Picante, NET WT./PESO NETO 4 oz. (113g), PRODUCT OF SPAIN "WILD FISH", GOYA FOODS, INC., Secaucus N.J. 07096.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1923-2017·2017-05-10

    Merge Healthcare Recalls Schiller CO2 Sensors Due to Alarm Bias

    Merge Healthcare is recalling 23 Schiller CO2 sensors that may display false clogging alarms, potentially adding bias to CO2 measurements and affecting alarm notifications.

    Product
    Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional accessory (sold separately) to the Merge Hemo Patient Data Module (PDM). The PDM is a major component of the Merge Hemo system.
    Category
    Medical Device
    Distribution
    10 states
  • HighFDA (Food)·F-2177-2017·2017-05-10

    Trail's End Chicago Sports Collection Snack Tins Recalled for Salmonella Risk

    Weaver Popcorn Co. is recalling Trail's End Chicago sports collection snack tins due to potential Salmonella contamination.

    Product
    Trail's End Chicago Cubs Sweet and Savory Collection Trail's End Chicago Cubs Chocolate Lover's Collection Trail's End Chicago Blackhawks Collection Tin Snack mixes containing: Chocolate Caramel Corn; Chocolate Pretzels; White Chocolate Pretzels; White Cheddar Popcorn…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2165-2017·2017-05-10

    Goya Octopus in Vegetable Oil Recalled for Squid Mislabeling

    Tradewind Foods is recalling Goya Octopus in Vegetable Oil because the product contains squid instead of octopus, posing a risk to consumers with seafood allergies.

    Product
    Goya Octopus in Vegetable Oil, Pulpo en Aceite Vegetal, NET WT./PESO NETO 4 oz. (113g), PRODUCT OF SPAIN "WILD FISH", GOYA FOODS, INC., Secaucus N.J. 07096.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1900-2017·2017-05-10

    Bard MR GHIATAS Beaded Breast Localization Wire Recalled for Compatibility Risk

    Bard Peripheral Vascular Inc. is recalling 570 units of MR GHIATAS Beaded Breast Localization Wire because they may be non-MR compatible instead of MR compatible.

    Product
    MR GHIATAS Beaded Breast Localization Wire, Product Code: 477201, 479201 Product Usage: The GHIATAS Beaded Breast Localization Wire consists of an introducer needle and asemi-rigid localization wire that are intended for use during breast lesion surgery as a guidefor the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1897-2017·2017-05-10

    BD FlowSmart Set MiniMed Pro-set Recalled for Bent Catheters

    Becton Dickinson is recalling 57,750 units of BD FlowSmart Set MiniMed Pro-set in California due to reports of bent catheters causing high blood glucose.

    Product
    BD FlowSmart Set MiniMed Pro-set Rx Only Distributed by Medtronic MiniMed Inc. 8006464633 8185765555 Legal Manufacturer Becton, Dickinson and Company USA BD Medical-Diabetes Care Becton Dickinson France SAS
    Category
    Medical Device
    Distribution
    1 state
  • HighCPSC·17148·2017-05-10

    AM Conservation Group Recalls Luminescent Night Lights Due to Fire Hazard

    AM Conservation Group is recalling about 37,000 luminescent night lights because they can overheat and pose a fire hazard. Consumers should stop using the products and contact the firm for a free replacement.

    Product
    Luminescent night lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1921-2017·2017-05-10

    Roho Sensor Ready Cushions Recalled for Improper Setup Risk

    Roho Inc. is recalling 5,646 units of ROHO High and Mid Profile cushions because the Smart Check tool may cause improper inflation, increasing the risk of skin or soft tissue injury.

    Product
    ROHO HIGH PROFILE Single Compartment Cushion with Sensor Ready Technology and ROHO MID PROFILE Single Compartment Cushion with Sensor Ready Technology.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1901-2017·2017-05-10

    Breg Inc Recalls Sterile Dressings Due to Unsealed Pouches

    Breg Inc is recalling sterile dressings (P/N 02328) because a small percentage may have unsealed pouches, rendering them non-sterile.

    Product
    Dressing Knee/Shldr, P/N 02328 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy pad and the skin. Sterile dressings are typically applied in a non-sterile environment after post-op and on occasion may be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1927-2017·2017-05-10

    Dale Medical Stabilock Endotracheal Tube Holder Recall for Adhesive Failure

    Dale Medical Products is recalling Stabilock Endotracheal Tube Holders because the adhesive faceplate may lose its properties and fail to adhere to the patient's face.

    Product
    Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Dale Stabilock Endotracheal Tube Bolder 270 is a 2 piece device consisting of an adhesive base, Dale product number 273, that attaches to the patient's skin and a cushioned neckband with tube channel that…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-050917·2017-05-09

    FSIS Public Health Alert for Frozen Pork and Chicken Due to Listeria

    The USDA FSIS issued a public health alert for frozen ready-to-eat fried chicken and pork sausage products due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    FSIS Issues Public Health Alert for Pork and Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide