The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

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.

8526–8550 of 29123

  • SevereNHTSA·21V183000·2021-03-17

    Braun Recalls Demers Ambulances Due to Sliding Seat Locking Pin Defect

    Braun Ambulances is recalling certain 2019-2021 Demers ambulances because the sliding attendant seat locking pin may fail, increasing injury risk in a crash.

    Product
    DEMERS AMBULANCES — DEMERS AMBULANCES MX170E FORD E-SERIES, TYPE I (MXP170E)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1217-2021·2021-03-17

    FDA Recalls CervAlign Anterior Cervical Plate System Due to Locking Mechanism Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 38mm Material Number: 66-238 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1246-2021·2021-03-17

    Medtronic Guide Catheter Recalled Due to Potential Sterility Compromise

    Medtronic Vascular is recalling 9 units of 6F Launcher Guide Catheters because unsealed pouches may compromise sterility.

    Product
    Medtronic 6F Launcher Guide Catheter 100 cm JR 4.0 Model Number: LA6JR40
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1205-2021·2021-03-17

    FDA Recalls CervAlign Anterior Cervical Plate System Due to Locking Mechanism Failure

    RTI Surgical is recalling CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 12mm Material Number: 66-112 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0335-2021·2021-03-17

    Green City Distribution Recalls Al-Riyan Tuna Meat Due to High Histamine Levels

    Green City Distribution is recalling Al-Riyan Tuna Meat in Vegetable Oil because of high levels of histamines. The product was distributed in California, Michigan, Tennessee, and New York.

    Product
    Al-Riyan Tuna Meat in Vegetable oil 7 oz. can 48 cans per case
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1243-2021·2021-03-17

    CervAlign Anterior Cervical Plate System Recalled for Locking Mechanism Failure

    RTI Surgical is recalling CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 22mm Material Number: 66-122 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V179000·2021-03-16

    Highland Ridge RV Recalls Fifth Wheels and Travel Trailers Due to Gas Leak Risk

    Highland Ridge RV is recalling 2019-2020 fifth wheels and travel trailers because an overtightened bolt may damage the stove's O-ring seal, causing a gas leak and increasing fire risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW MESA RIDGE, OPEN RANGE, SILVERSTAR, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V180000·2021-03-16

    Jayco Recalls 2021 Embark and Reatta Motorhomes Due to Gas Leak Risk

    Jayco is recalling 2021 Embark and Entegra Reatta motorhomes because an incorrectly routed LP furnace hose may cause a gas leak, increasing the risk of fire or explosion.

    Product
    JAYCO — JAYCO, ENTEGRA EMBARK, REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V181000·2021-03-16

    Peterbilt 536 Recalled for Engine Control Module Software Defect

    PACCAR is recalling one 2021 Peterbilt 536 truck because incorrect engine software may prevent safety features like braking and stability control from functioning properly.

    Product
    PETERBILT — PETERBILT 536
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V174000·2021-03-12

    ARBOC Specialty Vehicles Recalls 2021 Spirit of Freedom Due to Fuel Leak

    ARBOC is recalling 29 units of the 2021 Spirit of Freedom because a fuel hose may not be secured correctly, creating a fire risk.

    Product
    ARBOC SPECIALTY VEHICLES — ARBOC SPECIALTY VEHICLES SPIRIT OF FREEDOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V165000·2021-03-11

    Honda Recalls 2019-2020 Pilot and Passport Vehicles for Tire Defect

    Honda is recalling 2019-2020 Pilot and Passport vehicles equipped with specific Continental tires that may have been overcured during production, posing a risk of tire failure and loss of vehicle control.

    Product
    HONDA — HONDA PILOT, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V169000·2021-03-11

    Nissan Recalls Altima and Titan Vehicles for Tire Sidewall Defect

    Nissan is recalling 2018-2021 Titan and 2019-2020 Altima vehicles equipped with Continental tires that may have been over-cured, posing a risk of sudden air loss and loss of vehicle control.

    Product
    NISSAN — NISSAN TITAN, ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V170000·2021-03-11

    Nissan Recalls 2020 Murano Vehicles for Steering Link Defect

    Nissan is recalling 2020 Murano vehicles because a steering transverse link may separate, potentially causing loss of vehicle control and increasing crash risk.

    Product
    NISSAN — NISSAN MURANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V160000·2021-03-10

    Hyundai Recalls Genesis Vehicles Due to ABS Module Fire Risk

    Hyundai is recalling 2015-2020 Genesis and G80 vehicles because the ABS module could short circuit and cause a fire. Owners should park outside until the fuse is replaced.

    Product
    GENESIS — GENESIS, HYUNDAI G80, GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V162000·2021-03-10

    Mazda Recalls 2007-2009 B-Series Trucks for Air Bag Inflator Defect

    Mazda is recalling 2007-2009 B-Series trucks because the driver's side air bag inflator may explode, posing a risk of serious injury or death to occupants.

    Product
    MAZDA — MAZDA B-SERIES TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V155000·2021-03-10

    Ford Recalls 15,769 Vehicles Due to Tire Curing Defect

    Ford is recalling 15,769 vehicles equipped with Continental tires that may have been over-cured during production. This defect can cause sudden air loss or tread loss, increasing the risk of a crash.

    Product
    FORD — FORD F-150, F-350 SD, F-250 SD, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1159-2021·2021-03-10

    ReNovo Recalls Reprocessed Medical Devices Shipped as Sterile

    ReNovo, Inc. is recalling 81 units of reprocessed medical devices that were shipped to customers labeled as sterile but were non-sterile.

    Product
    Various reprocessed products: PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO; PROVISION Reprocessed Depy Mitek Ablation Electrodes, VAPR COOLPULSE 90 deg; PROVISION Reprocessed Smith and Nephew Trocars/ Cannulas (Class I); PROVISION Reprocessed Con
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V158000·2021-03-10

    Ford Recalls Vehicles for Driver-Side Airbag Inflator Explosion Risk

    Ford is recalling specific 2006-2012 vehicles because the driver-side airbag inflator may explode, potentially causing serious injury or death.

    Product
    MERCURY — MERCURY, LINCOLN, FORD MILAN, MKZ, ZEPHYR, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1156-2021·2021-03-10

    Hamilton Heater Shaker Recalled Due to Fire Risk from Flammable Liquids

    Hamilton Co is recalling 4,729 Heater Shaker units because flammable liquids entering the device can cause a fire.

    Product
    HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no condensation. REF 19903400
    Category
    Medical Device
    Distribution
    44 states
  • SevereNHTSA·21V150000·2021-03-09

    Autocar Recalls 2020 Legend Vehicles Due to Wiring Harness Defect

    Autocar is recalling 2020 Legend vehicles because a wiring harness may disconnect, causing loss of headlights and wipers. This increases the risk of a crash.

    Product
    AUTOCAR — AUTOCAR LEGEND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E017000·2021-03-08

    WP Dynamics Lift Kit Recall for Improperly Treated Bolts

    WP Dynamics is recalling ReadyLIFT Lift Kits for certain Ford and Dodge trucks because improperly heat-treated bolts may break, risking suspension separation and loss of vehicle control.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide