The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. 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.

22726–22750 of 32171

  • SevereNHTSA·15V405000·2015-06-24

    Shred-Tech MDS Vehicles Recalled for Front Axle Weight Rating Defect

    Shred-Tech is recalling specific MDS models because EPA emission controls cause the front axle to exceed its certified weight rating, increasing crash risk.

    Product
    SHRED-TECH — SHRED-TECH MDS-20GT, MDS-26GTX, MDS 2/26, MDS 1/26
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2441-2015·2015-06-24

    Whole Foods Market Muffin Bran Recalled for Undeclared Milk and Eggs

    Whole Foods Market is recalling Muffin Bran 6Pk packages due to undeclared milk and eggs. Consumers should check their pantries for affected products.

    Product
    BRAN Whole Foods Market Muffin Bran 6Pk packaged in clear plastic "clam shell" containers, NET WT. 12 oz., PLU 24857800499 Dist. by Whole Foods Market Austin, TX 78703
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Devices)·Z-1731-2015·2015-06-24

    HeartWare HVAD Recall Issued for Internal Controller Alarm Battery Failures

    HeartWare Inc. is recalling HVAD systems due to internal controller alarm battery failures. The recall affects 3,747 currently implanted devices worldwide.

    Product
    HeartWare Ventricular Assist System (HVAD). Catalog #'s US: 1101 and 1103 / OUS: 1100,1101,1102,1104,1104JP and 1205. For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure.
    Category
    Medical Device
    Distribution
    32 states
  • SevereFDA (Food)·F-2440-2015·2015-06-24

    Garber's Birthday Cake Ice Cream Recalled for Undeclared Egg Allergen

    Garber Ice Cream Company is voluntarily recalling Birthday Cake Flavored Ice Cream because eggs were added to the cake component, creating an undeclared egg allergen.

    Product
    Garber's Old Fashioned Ice cream, Birthday Cake Flavored 1.75 quarts, packed in a shrink wrap of 3. #1 lot of 211/ 3 pk produced on 12/12/13 expires on 12/12/14 #2 lot of 451/3 pk produced on 3/31/14 expires 3/31/15 #3 lot of 454/3 pk produced on 11/5 14 expires on…
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·15E053000·2015-06-23

    Suzuki Recalls VZR1800 Accessory Backrest Mounting Hardware Kits

    Suzuki is recalling accessory backrest mounting hardware kits for 2006-2015 VZR1800 motorcycles because incorrect bolts may contact the rear tire, increasing crash risk.

    Product
    SUZUKI — SUZUKI VZR1800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V396000·2015-06-22

    Turtle Top Transit Buses Recalled for Electrical Fire Risk

    Turtle Top is recalling certain 2006-2014 transit buses and specialty vehicles because a loose electrical connection may cause a fire.

    Product
    TURTLE TOP — TURTLE TOP ODYSSEY LT, ODYSSEY, TERRA TRANSPORT, VANTERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V393000·2015-06-22

    Jeep Cherokee Recall: Power Liftgate Module Fire Risk

    Chrysler is recalling 2014-2015 Jeep Cherokee vehicles with power liftgates because water intrusion may cause a short circuit and fire.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·094-2015·2015-06-20

    Shirk's Meats Recalls Pork and Beef Products Due to Listeria Risk

    Shirk's Meats is recalling approximately 2,478 pounds of pork and beef products in New York due to possible Listeria monocytogenes contamination.

    Product
    Timberline Meats, LLC — Shirk's Meats Recalls Pork and Beef Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·15V389000·2015-06-19

    MCI Motorcoaches Recalled for Hub Carrier Cracking and Oil Leaks

    Motor Coach Industries is recalling certain 2013-2015 D4500, D4505, and J4500 motorcoaches because hub carriers may crack or leak oil, potentially causing loss of vehicle control.

    Product
    MCI — MCI D4505, J4500, D4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15167·2015-06-19

    PetSmart Recalls Top Fin Plastic Aquarium Heaters Due to Electrical Shock Hazard

    PetSmart is recalling Top Fin plastic aquarium heaters due to an electrical problem that poses a risk of fire or electrical shock. Consumers should stop using the heaters and return them for a full refund.

    Product
    Top Fin Plastic Aquarium Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V390000·2015-06-19

    Forest River Recalls Trailers Due to Wheel Stud Breakage Risk

    Forest River is recalling specific model years of Auto Plus, Sandpiper, Vengeance, Cargo Mate, Hydra-Lift, and XLR trailers because wheel studs may break, potentially causing the wheel to detach.

    Product
    FOREST RIVER — FOREST RIVER HYDRA-LIFT, XLR, VENGEANCE, CARGO MATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2412-2015·2015-06-17

    Nuevotanicals Recalls Greenjoy Herbal Mind & Body Shot for Kratom Content

    Nuevotanicals is recalling Greenjoy Herbal Mind & Body Shots because the product contains Kratom. The recall covers products distributed in twelve states.

    Product
    100% NATURAL HERBAL MIND & BODY SHOT greenjoy Sustained, Relaxed Energy Supports Mood & Immune Functions Relief of pain for aging bodies HERBAL SUPPLEMENT 2.0 fl oz (59 mL) Formulated + MfG'd by NUEVOtanicals, LLC Fort Worth, Texas 76112 Distributed by: Scientific…
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·15V386000·2015-06-17

    Land Rover Recalls LR4 Vehicles Due to Sunroof Adhesive Defect

    Jaguar Land Rover is recalling 2012-2013 LR4 vehicles because the panoramic roof adhesive may not secure the assembly, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER LR4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V385000·2015-06-17

    Land Rover Recalls Range Rover Models for Door Latch Defect

    Jaguar Land Rover is recalling 2013-2016 Range Rover and 2014-2016 Range Rover Sport vehicles because doors may unlatch unexpectedly, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1767-2015·2015-06-17

    Philips Medical Systems Recalls Extended Brilliance Workstation UPS Accessories

    Philips Medical Systems is recalling Extended Brilliance Workstation UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Extended Brilliance Workstation (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1131-2015·2015-06-17

    Baxter Recalls Subpotent Heparin Sodium Injection Due to Raw Material Issues

    Baxter Healthcare is recalling specific lots of Heparin Sodium in Sodium Chloride Injection because the raw material was found to be subpotent and out of specification.

    Product
    HEPARIN SODIUM IN SODIUM CHLORIDE — HEPARIN SODIUM IN SODIUM CHLORIDE (HEPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1750-2015·2015-06-17

    ResMed Astral Ventilator Recall Due to Alarm Disabling Hazard

    ResMed is recalling Astral 100 and 150 ventilators because clinicians can disable all alarms, including circuit disconnection alerts, posing a risk of insufficient ventilation.

    Product
    Astral 100 ( Model No. 27001) & Astral 150 (Model No. 27003) ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2428-2015·2015-06-17

    Golden Krust Recalls Shrimp and Soya Patties Due to Undeclared Egg

    Golden Krust Caribbean Bakery is recalling Jamaican Style Shrimp & Soya Patties because they contain undeclared egg.

    Product
    Golden Krust SOYA PATTIES, NET WT. 17.2 LBS, 50 UNBAKED, KEEP FROZEN
    Category
    Food
    Distribution
    10 states