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.

22476–22500 of 50430

  • HighFDA (Devices)·Z-2724-2020·2020-08-05

    Medline Recalls ClearPro T-Piece Closed Suction Catheters Due to Assembly Failure

    Medline Industries is recalling 2,440 units of ClearPro T-Piece Closed Suction Catheters because reports indicate the catheter may come apart from the device assembly during use.

    Product
    ClearPro T-Piece Closed Suction Catheter, Model DYNCPTP14, 14 Fr 21.3 IN FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1043-2020·2020-08-05

    Giant Eagle Dried Island Fruit Mix Recalled for Undeclared Allergens

    Giant Eagle is recalling Dried Island Fruit Mix because it may contain undeclared peanut, almond, milk, and soy allergens.

    Product
    Giant Eagle Dried Island Fruit Mix , Net Wt. 10 oz. , 6 units per case. Packaging is a gusseted plastic resealable bag. Expiration date 01/15/2021
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2704-2020·2020-08-05

    United Imaging uCT 530 CT System Recalled for Sharp Metal Edge

    Shanghai United Imaging Healthcare is recalling four uCT 530 Computed Tomography X-ray Systems because uneven metal edge overlap may create a sharp edge.

    Product
    Computed Tomography X-ray System; Model uCT 530; Rx; UDI: (01) GTIN: 06971576831012 - Product Usage: intended to produce cross-sectional images of the body using computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2727-2020·2020-08-05

    Teleflex Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical Inc is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall covers 27,341 units distributed nationwide.

    Product
    Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2715-2020·2020-08-05

    Ion Beam Applications Recalls Proteus 235 Proton Therapy Systems

    Ion Beam Applications is recalling two Proteus 235 proton therapy systems because aborted irradiations cannot be resumed due to a software loading issue.

    Product
    Proteus 235 The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-2705-2020·2020-08-05

    United Imaging uCT 550 CT Systems Recalled for Sharp Metal Edges

    Shanghai United Imaging Healthcare is recalling three uCT 550 Computed Tomography X-ray Systems because uneven metal edges on the mylar strip may create sharp edges.

    Product
    Computed Tomography X-ray System; Model uCT 550; Rx; UDI: (01) GTIN: 06971576831036 - Product Usage: intended to produce cross-sectional images of the body using computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2701-2020·2020-08-05

    Abbott Alinity ci System Control Module Recalled for Quality Control Failures

    Abbott is recalling Alinity ci System Control Modules because quality control results were not properly evaluated for failures.

    Product
    Alinity ci series System Control Module (SCM); LN 3R70-01 Alinity ci series software versions, 3.1.1 and below
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2703-2020·2020-08-05

    United Imaging uCT 760 CT Systems Recalled for Sharp Metal Edges

    Shanghai United Imaging Healthcare is recalling five uCT 760 CT systems because uneven metal edges on the mylar strip may create sharp edges.

    Product
    Computed Tomography X-ray System; Model uCT 760; Rx; UDI: (01) GTIN: 06971576831043 - Product Usage: intended to produce cross-sectional images of the body using computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1413-2020·2020-08-05

    Lupin Recalls Lisinopril Tablets Due to Foreign Tablet Presence

    Lupin Pharmaceuticals is recalling specific bottles of 10 mg Lisinopril tablets because 20 mg tablets were found inside. Consumers should stop using the affected product.

    Product
    LISINOPRIL — LISINOPRIL (LISINOPRIL)
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Food)·F-1032-2020·2020-08-05

    Happy Colon Yum Shortbread Cookie Recalled for Undeclared Milk

    Happy Colon Foods is recalling Yum Shortbread Cookies because they contain butter but do not list milk as an ingredient.

    Product
    Happy Colon Yum Shortbread Cookie 0.98oz UPC 56817 00704
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-2733-2020·2020-08-05

    Arthrex Recalls Sterile Low Profile Titanium Bone Screws Due to Length Error

    Arthrex, Inc. is recalling 28 units of sterile low profile titanium bone screws because the screws are 5mm shorter than intended.

    Product
    Sterile Low Profile Screw, Titanium, 6.7 x 65mm Part Number: AR-8967-2865S - Product Usage: is intended to be used as a stand-alone bone screw, or in a plate-screw system for internal bone fixation for bone fractures, fusions, osteotomies and non-unions.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2713-2020·2020-08-05

    TTDEYE Radial Pink Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Radial Pink colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Radial Pink, B16112110 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2732-2020·2020-08-05

    Teleflex Medical Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical Inc. is recalling 29,740 Rusch Greenlite laryngoscopes because the welded joint may break. The devices are used for tracheal intubation.

    Product
    Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product Usage: The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2710-2020·2020-08-05

    TTDEYE Flower Brown Colored Contact Lenses Recalled for Lack of FDA Clearance

    Chengdu Ai Qin E-commerce Co., Ltd is recalling TTDEYE Flower Brown colored contact lenses because they were distributed without FDA clearance.

    Product
    TTDEYE (brand) Flower Brown, B16112210 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1044-2020·2020-08-05

    Kasugai Matcha Ame Candy Recalled for Undeclared Soybean Allergen

    J F C International Inc is recalling Kasugai brand Matcha Ame candy because the label fails to declare soybean, a major food allergen, present in the mold lubricant.

    Product
    Kasugai brand Matcha Ame (Green tea candy); 4.58 oz. plastic bag; 2 x 12 individual items per case Product of Japan Ingredients: glucose syrup, sugar, green tea powder, palm oil, artificial flavor. The label should include "mold lubricant oil (palm, rapseed, soybeans)…
    Category
    Food
    Distribution
    25 states
  • HighNHTSA·20V454000·2020-08-04

    Indian Recalls 2019 Scout Motorcycles Due to Brake Performance Issues

    Indian Motorcycle is recalling 2019 Scout, Scout Sixty, and Scout Bobber models because trapped air in the brake system may reduce performance and increase crash risk.

    Product
    INDIAN — INDIAN SCOUT BOBBER, SCOUT, SCOUT SIXTY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V453000·2020-08-04

    2019 Mercedes-Benz Sprinter Recalled for Fuel Pump Leak Risk

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because an open port on the fuel pump may leak fuel onto the roadway, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER (VS30)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V451000·2020-08-03

    Triumph Recalls 2020 Tiger 900 Models for Detaching Rear Reflectors

    Triumph is recalling 2020 Tiger 900 motorcycles because rear reflectors may detach, reducing visibility and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH TIGER 900 RALLY, TIGER 900, TIGER 900 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V452000·2020-08-03

    Bentley Recalls 2020 Flying Spur for Rear Camera Moisture Issue

    Bentley is recalling 2020 Flying Spur vehicles because moisture can enter the rear camera holder, reducing image clarity and increasing crash risk.

    Product
    BENTLEY — BENTLEY FLYING SPUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-08012020·2020-08-01

    USDA Alert: Frozen Taquitos and Chimichangas May Contain Hard Plastic

    USDA FSIS issued a public health alert for frozen taquitos and chimichangas that may contain hard plastic from recalled green chilies.

    Product
    Ajinomoto Foods North America — FSIS Issues Public Health Alert for Meat and Poultry Taquitos and Chimichangas Containing FDA-Regulated Diced Green Chilies That Have Been Recalled Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V449000·2020-07-31

    Mercedes-Benz Recalls Vehicles for Seat Belt Warning Software Defect

    Mercedes-Benz is recalling specific 2017-2019 models because instrument cluster software may cause the seat belt warning system to display a solid light instead of a blinking light with an audible tone.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLS 450, E 300, C 300, E 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V450000·2020-07-31

    Autocar Xpeditor Parking Brake May Apply Unexpectedly

    Certain 2018-2021 Autocar Xpeditor right-hand drive trucks may have improperly assembled parking brake plumbing, causing the brake to apply unexpectedly and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E053000·2020-07-31

    Walmart Recalls Hyper Tough 2 Ton Jack Stands Due to Collapse Risk

    Walmart is recalling specific Hyper Tough 2 Ton Jack Stands that may collapse unexpectedly under load, posing a risk of injury to nearby persons.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide