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.

24476–24500 of 50442

  • HighNHTSA·19V830000·2019-11-20

    Arcimoto Recalls 2019 FUV Motorcycles Due to Electrical Short Circuit Risk

    Arcimoto is recalling 25 units of the 2019 FUV motorcycle because a display board component may short circuit, potentially causing a sudden loss of power and increasing crash risk.

    Product
    ARCIMOTO — ARCIMOTO FUV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0152-2020·2019-11-20

    Harris Teeter Mint Chocolate Chip Ice Cream Recalled for Undeclared Soy

    Harris Teeter Supermarkets is recalling Mint Chocolate Chip Ice Cream because the ingredient soy was not declared in the product's ingredient statement or allergen declaration.

    Product
    Mint Chocolate Chip Ice Cream 1.5 QT (1.42L) container sold under the brand names of Harris Teeter ALL NATURAL, PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC MATTHEWS, NC 28105 UPC 0 72036 51151 5 & Lowes DISTRIBUTED BY: LOWES FOODS, LLC P.O. BOX 24908 WINSTON-SALEM, NC 27114-4908…
    Category
    Food
    Distribution
    3 states
  • HighCPSC·20025·2019-11-20

    Cutek Proclean Wood Restoration Recalled for FHSA Labeling Violations

    Deck Source is recalling Cutek Proclean Professional Wood Restoration because its label violates Federal Hazardous Substance Act requirements, posing a risk of poisoning.

    Product
    Cutek Proclean Professional Wood Restoration
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0372-2020·2019-11-20

    Draeger Infinity M300 Telemetry Devices Recalled for Cybersecurity Vulnerabilities

    Draeger Medical Systems is recalling Infinity M300 telemetry monitoring devices due to cybersecurity vulnerabilities including DDoS, Spoofing, and Tampering.

    Product
    Infinity M300 telemetry monitoring device Software versions VG2.3.1 and lower, Model Numbers MS25755, MS26076, MS26031, MS18623, MS22862, MS25301
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0402-2020·2019-11-20

    Orthofix Recalls Elbow Sterile Kits Due to Drill Bit Design Defect

    Orthofix Srl is recalling specific lots of Elbow Sterile Kits because drill bits have a geometrical detail that does not match the intended design, potentially lowering cutting performance.

    Product
    ORTHOFIX Catalogue Number: ref: 99-93504, ELBOW STERILE KIT, UDI: (01)18054242511533
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-0348-2020·2019-11-20

    Basic Reset Energy FX Recalled for Adulteration and Misbranding

    Basic Reset Inc. is recalling Energy FX products because FDA determined the marketing claims rendered the product a medical device that was adulterated and misbranded.

    Product
    Energy FX: a) original Aluminum (100-3A) b) sleek (adult and kid & pet) (100-3B)
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0137-2020·2019-11-20

    Riba Foods Recalls Arriba Bacon Salsa for Undeclared Milk

    Riba Foods Inc. is recalling Arriba! Bacon Salsa due to undeclared milk. The product was distributed in four states.

    Product
    Fire Roasted Medium Arriba! Bacon Salsa with Real Bacon NET WT 16 OZ. UPC Code: 033907 20513 1 packaged in a clear glass jar
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0153-2020·2019-11-20

    Harris Teeter Recalls Mint Chip Ice Cream for Undeclared Soy

    Harris Teeter is recalling Mint Chip Old Fashioned Ice Cream because soy was not declared in the ingredient statement or allergen declaration.

    Product
    THE FRESH MARKET Mint Chip OLD FASHIONED ICE CREAM 1.5 QT (1.42 L) container DISTRIBUTED BY: THE FRESH MARKET GREENSBORO, NC 27406 UPC 7 37094 01537 4
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0371-2020·2019-11-20

    Avanos Medical Recalls CORFLO PEG Kits Due to Connector Defect

    Avanos Medical is recalling CORFLO PEG Kits because the connector piece does not pass over the guidewire. The recall affects 104 cases distributed to six US states and Great Britain.

    Product
    CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit with ENFit Connector. 2 units per case The devices could be branded as Halyard Health.
    Category
    Medical Device
    Distribution
    6 states
  • HighFDA (Devices)·Z-0354-2020·2019-11-20

    Monarch Medical Technologies Recalls EndoTool SubQ Software Versions

    Monarch Medical Technologies is recalling EndoTool SubQ software versions 1.7.1, 1.7.4, and 1.7.5 because the product was distributed prior to FDA approval or clearance.

    Product
    EndoTool SubQ (Versions 1.7.1, 1.7.4, 1.7.5)
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-0396-2020·2019-11-20

    Orthofix Pelvis Sterile Kit Recalled for Drill Bit Design Defect

    Orthofix Srl is recalling specific lots of Pelvis Sterile Kits because drill bits have a design defect that may reduce cutting performance.

    Product
    ORTHOFIX Catalogue Number: ref: 99-93501US, PELVIS STERILE KIT, RX ONLY, UDI: (01)180S4242S11281
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Devices)·Z-0350-2020·2019-11-20

    PrivaPath Universal Sexual Health Testing Kit Recalled for Damaged Tubes

    PrivaPath Diagnostics is recalling Universal Sexual Health Testing Kits due to potential tube damage that may cause blood exposure or erroneous results.

    Product
    Universal Sexual Health Testing Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0150-2020·2019-11-20

    Harris Teeter Ice Cream Recalled for Undeclared Soy Allergen

    Harris Teeter is recalling Premium Selections Chocolate Satisfaction Ice Cream because the ingredient soy was not declared on the label.

    Product
    Harris Teeter PREMIUM SELECTIONS CHOCOLATE SATISFACTION ICE CREAM 1.5 QT (1.42L) container PROUDLY DISTRIBUTED BY: HARRIS TEETER. LLC, MATTHEWS, NC 28105 UPC 0 72036 43030 4
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0365-2020·2019-11-20

    Cadence Science Pressure Control Glass Syringes Recalled for Breakage Risk

    Cadence Science is recalling 237 Pressure Control Glass Syringes because they may break during use, posing a potential injury risk to patients and healthcare workers.

    Product
    Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340 (GTIN #816329023404); 5341 (GTIN #816329023411); 5342 (GTIN #816329023428); 5343 (GTIN #816329023435) - Product Usage: General Hospital Use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20024·2019-11-19

    Ontel ISO7X Isometric Exercise Devices Recalled for Projectile Hazard

    United National Closeout Stores is recalling about 1,500 Ontel ISO7X isometric exercise devices because handle grips can break and eject parts, posing an injury risk.

    Product
    ISO7X Isometric Exercise Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V829000·2019-11-19

    Freightliner Econic SD Recalled for Incorrect Axle Weight Rating Labels

    Daimler Trucks North America is recalling 2020 Freightliner Econic SD vehicles because certification labels contain incorrect gross axle weight rating information, which may lead to axle overloading.

    Product
    FREIGHTLINER — FREIGHTLINER ECONIC SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V831000·2019-11-19

    Thomas Built Buses Recalling Saf-T-Liner HDX School Buses for Torque Converter Defect

    Daimler Trucks North America is recalling 2018-2020 Thomas Built Saf-T-Liner HDX school buses because loose torque converter fasteners may disable the vehicle, increasing injury risk during evacuation.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19E079000·2019-11-15

    Triumph Recalls Quickshifter Kits for Speed Triple S Motorcycles

    Triumph is recalling aftermarket Quickshifter Kits for Speed Triple S motorcycles because the assembly may interfere with gear changes, increasing crash risk.

    Product
    POWER TRAIN:MANUAL TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V816000·2019-11-15

    Newmar Recalls 2020 Mountain Aire Motorhomes for Headlight Defect

    Newmar is recalling 2020 Mountain Aire motorhomes because low beam bulbs may fail to illuminate when high beams are activated, increasing crash risk.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20020·2019-11-14

    Kenmore Elite Microwave Ovens Recalled for Exterior Burn Hazard

    CPSC recalls Kenmore Elite microwave ovens sold at Sears due to incorrect wiring that causes the exterior to overheat, posing a burn risk.

    Product
    Kenmore Elite Microwave Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0285-2020·2019-11-13

    Red Mountain Compounding Pharmacy Recalls S-TEST CYP Vials for Sterility Concerns

    Red Mountain Compounding Pharmacy is recalling S-TEST CYP 200mg/ml vials nationwide due to a lack of assurance of sterility.

    Product
    S-TEST CYP 200MG/ML MDV IN ETHYL OLEATE OIL, Rx only, a) 5ml, b) 10 ml, c) 13ml glass vials, Red Mountain Compounding Rx.
    Category
    Drug
    Distribution
    Distributed nationwide