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.

26226–26250 of 50460

  • HighFDA (Devices)·Z-1039-2019·2019-03-27

    Shimadzu Mobile X-Ray System Recalled for Brake Failure

    Shimadzu is recalling 93 MobileDaRt Evolution mobile X-ray systems because the brakes may fail to engage when the operator releases the drive handle.

    Product
    SHIMADZU MobileDaRt Evolution (MX8 Version), Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1065-2019·2019-03-27

    Heritage Pharmaceuticals Recalls Subpotent Etomidate Injection Vials

    Heritage Pharmaceuticals is recalling 11,888 vials of Etomidate Injection because the drug was found to be subpotent. The recall is voluntary and nationwide.

    Product
    Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1178-2019·2019-03-27

    Horizon Food Group Recalls Ne-Mo's Red Velvet Cake Squares Due to Foreign Object

    Horizon Food Group is recalling Ne-Mo's Red Velvet Cake Squares after a complaint of a bird foot found in the product.

    Product
    Ne-Mo's Red Velvet Cake Square with Cream Cheese Icing, item 408-6; Net Wt. 3 oz. Case UPC: 2007606404086 7 Display pk 6 ea/pk UPC: 10076064040860 0 Individual unit UPC: 07606400408 7 Frozen product has a shelf life of 365 days from the date of production Refrigerated…
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1040-2019·2019-03-27

    Fujifilm FDR Go PLUS Mobile X-Ray System Recalled for Braking Defect

    Fujifilm is recalling 56 mobile X-ray systems because the braking mechanism may fail to engage when the handle is released.

    Product
    Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1170-2019·2019-03-27

    Arbre Farms Organic Green Beans Recalled for Listeria Risk

    Arbre Farms, Inc. is recalling Organic Green Beans, 1" cut, IQF 1500# tote, due to a potential Listeria monocytogenes contamination.

    Product
    Organic Green Beans, 1" cut, IQF 1500# tote
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1180-2019·2019-03-27

    Best Choice Pancake Mix Recalled for Undeclared Milk Allergen

    Gilster-Mary Lee Corp. is recalling Best Choice Pancake & Waffle Complete Mix Original because the product contains milk but the packaging does not declare it as an ingredient.

    Product
    Best Choice Pancake & Waffle Complete Mix Original 32oz. retail carton, 12 retail units per wholesale case. UPC# 70038 30212
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·19V240000·2019-03-27

    Thor Motor Coach Recalls 2018-2020 Models Due to Reversed Backup Camera Image

    Thor Motor Coach is recalling 110 motorhomes because the backup camera image may reverse, increasing crash risk. Dealers will install a harness to fix the issue.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FOUR WINDS, CHATEAU, MAGNITUDE, OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2019·2019-03-27

    ConvaTec Recalls Feeding Tubes Due to Potential Sterile Barrier Breach

    ConvaTec is recalling specific lots of Feeding Tube Metric devices because an internal assessment found a potential breach in the sterile barrier.

    Product
    Feeding Tube Metric, disposable, sterile, 100 eaches per sales unit. Labeled as: xray CH05/40CM and xray CH08/40CM Product Usage: Duodenal and Stomach Gastroenterology Tubes are sterile disposable devices which may be inserted through the nose or mouth via the esophagus into…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1019-2019·2019-03-27

    AAP Implantate Lambotte Chisel Recalled for Potential Breakage at Welded Parts

    AAP Implantate AG is recalling 25 units of the 20 mm Lambotte chisel due to a potential risk of breaking at the welded piece parts of the chisel body and knocking plate.

    Product
    aap Implante AG, Lambotte chisel, 20 mm, REF IU 3000-20 Product Usage: Surgical instruments are intended to aid in the insertion of bone plates and screws as well as for reduction and support during orthopedic surgeries. If not otherwise specified, instruments are intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1021-2019·2019-03-27

    Advanced Pharma Recalls Glycopyrrolate Syringes Due to Sterility Concerns

    Advanced Pharma Inc. is recalling 2,580 syringes of Glycopyrrolate Injectable Solution nationwide due to a lack of assurance of sterility.

    Product
    Glycopyrrolate Injectable Solution 1 mg/5 mL (0.2 mg per mL), Sterile single use syringe, NDC: 42852-828-67 Avella of Houston 9265 Kirby Dr., Houston, TX 77054 (877) 794-0404
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·19V243000·2019-03-27

    Osco Recalls Emergency Vehicles With Faulty Brake Light Wiring

    Osco Tank & Truck Sales is recalling 16,342 emergency vehicles built on 2012 Kenworth T440 and 2018 Peterbilt 348 chassis because brake lights may illuminate without the pedal being pressed.

    Product
    KENWORTH — KENWORTH, PETERBILT T440, 348
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V244000·2019-03-27

    Toyota Recalls 2019 Models Due to Illegible Load Capacity Labels

    Toyota is recalling specific 2019 models because the load capacity label text may become illegible, potentially leading to vehicle overload and increased crash risk.

    Product
    TOYOTA — TOYOTA CAMRY, AVALON, PRIUS, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V241000·2019-03-27

    Volkswagen Recalls 2019 Tiguan LWB for Inaccurate Tire Information Label

    Volkswagen is recalling 2019 Tiguan LWB vehicles because the tire information label contains inaccurate dimension and pressure specifications, which may increase crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1175-2019·2019-03-27

    Jansal Valley Chocolate Covered Almonds Recalled for Undeclared Sesame

    Friendly Fruit Market is recalling Jansal Valley Cocoa Dusted Chocolate Covered Almonds because the product contains undeclared sesame seeds.

    Product
    JANSAL VALLEY Cocoa Dusted Chocolate Covered Almonds, Net Weight: 6 OZ (170 G), packed in a plastic clamshell, UPC: 7 08152 32988 7
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1037-2019·2019-03-27

    ConvaTec Recalls Nelaton Urinary Catheters Due to Sterile Barrier Breach Risk

    ConvaTec is recalling Nelaton Urinary Catheters because an internal assessment found a potential breach in the sterile barrier, which could compromise the device's sterility.

    Product
    Nelaton Urinary Catheter, disposable, sterile, 100 eaches per sales unit. Labeled as: CH16/40CM and CH14/40CM Product Usage: Urinary Catheters are sterile disposable devices intended to provide an intermittent pathway for drainage of fluids from the bladder. They are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1173-2019·2019-03-27

    DAHlicious Organic Lassi Recalled for Improper Pasteurization

    DAHlicious is recalling 1,296 bottles of Organic Lassi Golden Turmeric due to improper pasteurization. Consumers should stop consuming the product.

    Product
    DAHlicious ORGANIC LASSI India-Style DRINKABLE YOGURT Golden Turmeric Lassi, 23 FL OZ (946 mL), UPC: 7 93573 01476 4.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1177-2019·2019-03-27

    Horizon Food Group Recalls Ne-Mo's Chocolate Cake Squares Due to Foreign Object

    Horizon Food Group is recalling Ne-Mo's Chocolate Cake Squares with Cream Cheese Icing after a complaint of a bird foot found in the product.

    Product
    Ne-Mo's Chocolate Cake Square with Cream Cheese Icing, item 104; Net Wt. 3 oz. Case UPC: 2007606401046 4; Display pk 6 ea/pk UPC: 10076064010460 7 Individual unit UPC: 07606400104 8 Frozen product has a shelf life of 365 days from the date of production Refrigerated…
    Category
    Food
    Distribution
    20 states
  • HighCPSC·19091·2019-03-27

    Cambridge Elevating Recalls Home Elevators Due to Fall Hazard

    Cambridge Elevating is recalling approximately 680 home elevators because the landing door can unlock without the elevator present, posing a fall hazard.

    Product
    Home elevators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1179-2019·2019-03-27

    Horizon Food Group Recalls Ne-Mo's Birthday Cake Squares Due to Foreign Object

    Horizon Food Group is recalling Ne-Mo's Birthday Cake Squares with Buttercream Icing after a complaint that a bird foot was found in the product.

    Product
    Ne-Mo's Birthday Cake Square with Buttercream Icing, item 506-6; Net Wt. 3 oz. Case UPC: 2007606405066 8 Display pk 6 ea/pk UPC: 10076064050660 1 Individual unit UPC: 07606405066 4 Frozen product has a shelf life of 365 days from the date of production Refrigerated…
    Category
    Food
    Distribution
    20 states
  • HighFDA (Devices)·Z-1027-2019·2019-03-27

    CP Medical Recalls Sterile Surgical Sutures Due to Potential Sterility Compromise

    CP Medical Inc is recalling Plain and Chromic Gut Absorbable Surgical Sutures because routine endotoxin testing showed an out-of-limit result, potentially compromising sterility.

    Product
    Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic procedures, but not for use in cardiovascular and neural…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1020-2019·2019-03-27

    FDA Recalls 850 Units of Covidien Force TriVerse Electrosurgical Devices

    The FDA is recalling 850 units of the Covidien Force TriVerse electrosurgical device due to potential sterile packaging compromise.

    Product
    Covidien Force TriVerse electrosurgical device 10 cord-Intended as electrosurgical energy to cut and/or coagulate tissue. Product Usage: Single-use device intended for use in open procedures (such as general, urologic, thoracic, plastic and reconstructive, gynecologic) and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V238000·2019-03-26

    Vantage Recalls Shuttle Vehicles with Defective Foldaway Seat Locks

    Vantage Mobility is recalling specific shuttle vehicles equipped with Freedman GO-3S foldaway seats because the seat cushion may not remain locked in place during a crash or sudden stop.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FORD, FREIGHTLINER SPRINTER 3500, SPRINTER 2500, TRANSIT, F-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V239000·2019-03-26

    Custom Fab & Body Recalls Emergency Vehicles with Faulty Brake Lights

    Custom Fab & Body is recalling specific 2017-2018 emergency vehicles because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    KENWORTH — KENWORTH, FORD, INTERNATIONAL T370, F-650 SD, WORKSTAR, DURASTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide