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.

22451–22475 of 50429

  • HighFDA (Food)·F-1049-2020·2020-08-12

    Dietary Supplements Recalled for Undeclared Soy Allergen

    Provident Nutraceutical is recalling 95 bottles of various branded dietary supplements because they may contain undeclared soy.

    Product
    Dietary supplements, 60 capsules, UPC 15033-61832, Product # 832060, labeled under the following brands and product names, packaged in white plastic bottle with black plastic lid: 1. Aspire Rejuvenation Nutraceuticals, Tranquility PM, Mfg for: Aspire Rejuvenation…
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·20V472000·2020-08-11

    Triumph Recalls 2019-2020 Motorcycles Due to Wiring Harness Defect

    Triumph is recalling 2019-2020 Street Scrambler and Street Twin motorcycles because a misrouted wiring harness may contact the frame, causing the engine to stall and increasing crash risk.

    Product
    TRIUMPH — TRIUMPH STREET SCRAMBLER, STREET TWIN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E054000·2020-08-10

    Kiel Recalls Avance Passenger Seats Due to Seat Belt Defect

    Kiel is recalling specific Avance passenger seats for motorcoaches because the seat belt retractors may not function properly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V468000·2020-08-10

    Entegra Qwest motorhome wiring defect may cause airbag malfunction

    Jayco is recalling 2020-2021 Entegra Qwest motorhomes and related Jayco models because front seat wiring harnesses may be routed incorrectly, creating a risk of unexpected or failed airbag deployment.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE PRESTIGE, QWEST, MELBOURNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-08072020-01·2020-08-07

    USDA Issues Public Health Alert for Blue Grass Sausage Due to Listeria

    USDA issued a public health alert for Blue Grass Provisions ready-to-eat sausages due to possible Listeria contamination. Products were produced in April 2020 and are past their use-by dates.

    Product
    Blue Grass Provisions Co. Inc. — FSIS Issues Public Health Alert for Ready to Eat Sausage Products due to Possible Listeria Contamination
    Category
    Food
    Distribution
    4 states
  • HighNHTSA·20V465000·2020-08-07

    BMW Recalls 2020 X5 and X7 Models Due to Starter Motor Bolt Risk

    BMW is recalling 21 vehicles because an extra bolt in the starter motor could fall into the transmission, causing an engine stall and increasing crash risk.

    Product
    BMW — BMW X7, X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V461000·2020-08-06

    GM Recalls 2020 Chevrolet Corvette for Front Trunk Release Defect

    General Motors is recalling 2020 Chevrolet Corvette vehicles because the front trunk release button may fail to function after the vehicle is shut off for ten minutes, potentially trapping a person inside.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20769·2020-08-06

    REVIVE Essential Oils Recalled for Non-Child-Resistant Packaging and Poisoning Risk

    REVIVE is recalling specific essential oils and blends because the packaging is not child-resistant, posing a risk of poisoning if swallowed by young children.

    Product
    REVIVE Wintergreen and Birch Essential Oils and REVIVE Sore No More, Ache Away and Breeze Essential Oil Blends
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2708-2020·2020-08-05

    TTDEYE Black Starshine Colored Contact Lenses Recalled for Lack of FDA Clearance

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

    Product
    TTDEYE (brand) Black Starshine, B16112100 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2020·2020-08-05

    Teleflex Rusch Greenlite Laryngoscopes Recalled for Welded Joint Breakage

    Teleflex Medical Inc. is recalling Rusch Greenlite laryngoscopes because the welded joint may break. The recall affects 75,320 units distributed nationwide.

    Product
    Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (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-2712-2020·2020-08-05

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

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

    Product
    TTDEYE (brand) Radial Brown, B16112109 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1033-2020·2020-08-05

    Happy Colon Chocolate Chip Cookies Recalled for Undeclared Milk

    Happy Colon Foods is recalling specific chocolate chip cookies because they contain butter but do not list milk as an ingredient.

    Product
    Happy Colon MMMM Chocolate Chip Cookie 0.98oz UPC 56817 00703
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-1047-2020·2020-08-05

    Stick-E Fingers Barbecue Rub Recalled for Undeclared Milk Allergen

    Stick E Fingers BBQ LLC is recalling 181 jars of All Purpose Rub because the label declares butter but fails to list milk or buttermilk.

    Product
    Stick-E Fingers Barbecue All Purpose Rub is a dry rub, packaged in 13.2 oz plastic jar, UPC 8 60003 24004 5. No company's address listed on the label. The product label is read in parts: "***STICK-E FINGERS BARBECUE***All Purpose Rub *** INGREDIENTS: SALT, ONION, BUTTER…
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2707-2020·2020-08-05

    Medtronic StealthStation S7 System Recalled for Navigation Inaccuracy

    Medtronic is recalling two StealthStation S7 Systems with Polaris Spectra Cameras due to a manufacturing issue that may cause 6mm navigation inaccuracy when using specific trackers.

    Product
    StealthStation" S7 System with Polaris Spectra Camera part number PSU 9733437 - Product Usage: are intended as an aid for precisely locating anatomical structures in either open or percutaneous procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2730-2020·2020-08-05

    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 devices are used for tracheal intubation.

    Product
    Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (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
  • HighCPSC·20160·2020-08-05

    WD-40 Recalls X-14 Mildew Stain Remover Due to Skin Irritation Risk

    WD-40 Company is recalling specific 16 and 32-ounce bottles of X-14 Mildew Stain Remover because pressure buildup may cause leaks and skin irritation.

    Product
    X-14® Mildew Stain Remover
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V458000·2020-08-05

    Thor Motor Coach Motorhomes Recalled: Pedestal Bolts May Fail During Crash

    Thor Motor Coach is recalling 2020-2021 Daybreak, 2018-2021 Four Winds, and 2018-2021 Chateau motorhomes because barrel chair pedestals are secured with bolts of the wrong size. In a crash, these pedestals could separate, causing seat belt anchorages to fail and increasing injury risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH redundant FOUR WINDS, redundant CHATEAU, DAYBREAK, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-08052020-01·2020-08-05

    USDA Alerts on Ready-to-Eat Meat and Poultry with Recalled Onions

    USDA FSIS issued a public health alert for ready-to-eat meat and poultry products containing onions recalled due to possible Salmonella Newport contamination.

    Product
    Taylor Farms TX, Inc. — FSIS Issues Public Health Alert for Ready-to-Eat Meat and Poultry Products Containing FDA-Regulated Onions that have been Recalled due to Possible Salmonella Newport Contamination
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2714-2020·2020-08-05

    TTDEYE Devil Red Colored Contact Lenses Recalled for Lack of FDA Clearance

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

    Product
    TTDEYE (brand) Devil Red, B16112201 - Product Usage: Colored contact lenses
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2728-2020·2020-08-05

    Teleflex Medical Recalls Rusch Greenlite Laryngoscopes Due to Welded Joint Breakage

    Teleflex Medical Inc. is recalling 7,401 Rusch Greenlite laryngoscopes because the welded joint may break during use.

    Product
    Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (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-2731-2020·2020-08-05

    Teleflex Rusch Greenlite Laryngoscopes Recalled for Welded Joint Breakage

    Teleflex Medical is recalling Rusch Greenlite laryngoscopes because the welded joints may break. The devices are used for tracheal intubation.

    Product
    Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (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-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