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.

20851–20875 of 32121

  • SevereFDA (Drugs)·D-0584-2016·2016-01-27

    Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Particulates

    Pine Pharmaceuticals is recalling specific lots of bevacizumab syringes for intravitreal injection because they contain silicone oil microdroplets.

    Product
    Bevacizumab 2.5 mg/0.1 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal injection, Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0671-2016·2016-01-27

    MWT Materials Recalls Accusorb MRI Leg Wrap Blankets Due to Overheating Risk

    MWT Materials, Inc. is recalling 47 units of Accusorb MRI Leg Wrap Blankets because they may overheat when not used correctly, posing a risk of patient injury.

    Product
    Accusorb MRI MAC7009 Part Number: MRI-09 MRI- Leg Wrap Blanket Various Sizes Product Usage: Radio frequency shielding blankets and body-part covers for the MRI environment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E007000·2016-01-27

    Continental Air Bag Control Units Recalled for Corrosion Risk

    Continental is recalling Air Bag Control Units manufactured between 2006 and 2010 because a power supply component may corrode, potentially preventing air bags from deploying in a crash.

    Product
    AIR BAGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0580-2016·2016-01-27

    FDA Recalls Energique Homeopathic Pain Spray for Microbial Contamination

    Grato Holdings is recalling Energique First Aid Pain & Trauma Relief homeopathic spray due to out-of-specification microbial counts.

    Product
    Energique, Homeopathic Remedy, First Aid Pain & Trauma Relief, 1 fl oz (30 ml) bottles, NDC 44911-0135-1, Dist. by Energique, Inc., Woodbine, IA; ALSO LABELED AS --- Liddell Laboratories, First Aid Pain & Trauma Relief, Topical Homeopathic Spray, NDC 50845-0216-1, Dist By…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0598-2016·2016-01-27

    Brainlab Cranial Navigation System Recalled for Potential Software Inaccuracy

    Brainlab AG is recalling its Cranial Navigation System software due to a potential error that may cause inaccurate instrument display during surgery.

    Product
    Brainlab Cranial Navigation System: An Image Guided Surgery System / Stereotactic. Radiology Departments. The BrainLAB Cranial IGS System is intended to be an intra-operative image guided localization system to enable minimally invasive surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0570-2016·2016-01-27

    Amerita Recalls Baclofen and Clonidine Syringes Due to Sterility Concerns

    Amerita Specialty Infusion Services is recalling specific lots of compounded intrathecal syringes because the company cannot ensure they are sterile.

    Product
    IT Custom Compound (BC) Baclofen 2000 mcg/ml, Clonidine 2 mcg/ml 40 ml PF syringe, FOR INTRATHECAL USE ONLY, Rx Only, Compounded by Amerita, Inc., Prescott, AZ 86305-1614
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0582-2016·2016-01-27

    Pine Pharmaceuticals Recalls Bevacizumab Syringes Due to Silicone Oil Microdroplets

    Pine Pharmaceuticals is recalling specific lots of bevacizumab syringes for intravitreal use due to the presence of silicone oil microdroplets.

    Product
    Bevacizumab 1.25 mg/0.05 mL filled to 0.06 mL in 3/10 mL 31 G 5/16" Syringe for intravitreal, Rx -- Pine Pharmaceuticals, 100 Colvin Woods Pkwy Suite 300, Tonawanda, NY 14150.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V037000·2016-01-26

    Altec Recalls 2015 Effer Knuckle Boom Cranes Due to Pedestal Cracks

    Altec Industries is recalling 2015 Effer 440 and 470 Knuckle Boom Cranes because pedestal welds may crack, potentially causing the crane to fall and injure people.

    Product
    EFFER — EFFER 440 KNUCKLE BOOM CRANE, 470 KNUCKLE BOOM CRANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E006000·2016-01-25

    Takata Recalls Driver-Side Air Bag Inflators in Multiple Vehicle Brands

    Takata is recalling driver-side air bag inflators in Audi, Ford, Mazda, Sprinter, and Volkswagen vehicles that may rupture during deployment.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V035000·2016-01-25

    Volkswagen Recalls Touareg Hybrids for Battery Fire Risk

    Volkswagen is recalling 2011-2015 Touareg Hybrid vehicles because water in the battery tray may cause an electrical short and fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN TOUAREG HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E005000·2016-01-25

    Takata Recalls Driver-Side Frontal Air Bag Inflators Due to Rupture Risk

    Takata is recalling specific driver-side frontal air bag inflators that may rupture during deployment, potentially causing serious injury or death to vehicle occupants.

    Product
    AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V029000·2016-01-22

    Nissan Recalls 2013-2015 Altima Vehicles for Hood Latch Defect

    Nissan is recalling 2013-2015 Altima vehicles because the secondary hood latch may fail to engage, allowing the hood to open while driving.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V027000·2016-01-21

    Rosenbauer Recalls 2015 Commander Fire Trucks Due to Axle Nut Issue

    Rosenbauer is recalling 2015 Commander fire trucks because improperly tightened axle nuts could cause the driveshaft to disconnect, increasing crash risk.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V024000·2016-01-21

    Rosenbauer Commander Fire Trucks Recalled for Steering Control Loss Risk

    Rosenbauer is recalling 2014-2015 Commander fire trucks because loose ball joints in certain front suspension assemblies could separate, causing a loss of steering control.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V026000·2016-01-21

    Winnebago Recalls 2015-2016 Motorhomes Due to Ignition Switch Defect

    Winnebago is recalling 2015-2016 Travato, Trend, and Itasca Viva! motorhomes because an ignition switch defect may cause the vehicle to stall or disable safety systems.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA TREND, TRAVATO, VIVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V025000·2016-01-21

    Vanguard Recalls 2014-2015 Dry Freight Van Trailers Due to Brake Drag

    Vanguard is recalling 2014-2015 Dry Freight Van Trailers because improperly seated brake diaphragms may cause drag, potentially leading to wheel end fires.

    Product
    VANGUARD — VANGUARD DRY FREIGHT VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E004000·2016-01-21

    Meritor Trailer Axle Recall for Brake Drag Fire Risk

    Meritor is recalling certain trailer axle assemblies equipped with specific air brake actuators that may experience brake drag, posing a risk of wheel end fire.

    Product
    SERVICE BRAKES, AIR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0369-2016·2016-01-20

    Sockeye Suzy Fish Recalls Smoked Spring Chinook Cans for Botulism Risk

    Sockeye Suzys Fish LLC is recalling 13,281 cans of Smoked Spring Chinook in Oregon and Washington due to potential Clostridium botulinum contamination.

    Product
    Smoked Spring Chinook, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67402 9, UPC 7 48252 67382 4, UPC 7 48252 67372 5
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0366-2016·2016-01-20

    Sockeye Suzy Fish Recalls Smoked Jalapeno Sturgeon Cans

    Sockeye Suzys Fish LLC is recalling 13,281 cans of Smoked Jalapeno Sturgeon due to potential Clostridium botulinum contamination.

    Product
    Smoked Jalapeno Sturgeon, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67272 8
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0363-2016·2016-01-20

    Sockeye Suzy Fish Recalls Smoked Garlic Steelhead Cans

    Sockeye Suzys Fish LLC is recalling 13,281 cans of Smoked Garlic Steelhead due to potential Clostridium botulinum contamination. The product was distributed in Oregon and Washington.

    Product
    Smoked Garlic Steelhead, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67362 6
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0362-2016·2016-01-20

    Sockeye Suzy Fish Recalls Smoked Garlic Chinook Salmon Cans

    Sockeye Suzys Fish LLC is recalling 13,281 cans of Smoked Garlic Chinook Salmon due to potential Clostridium botulinum contamination.

    Product
    Smoked Garlic Chinook (salmon), Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67222 3
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0358-2016·2016-01-20

    Sockeye Suzy Fish Recalls Peppered and Smoked Sockeye Cans

    Sockeye Suzys Fish LLC is recalling 13,281 cans of Peppered & Smoked Sockeye due to potential Clostridium botulinum contamination.

    Product
    Peppered & Smoked Sockeye, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67232 2
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0372-2016·2016-01-20

    Sockeye Suzy Fish Recalls Smoked Walleye Cans Due to Botulism Risk

    Sockeye Suzys Fish LLC is recalling 13,281 cans of smoked walleye in Oregon and Washington due to potential Clostridium botulinum contamination.

    Product
    Smoked Walleye, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 94504 39610 2
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0357-2016·2016-01-20

    Sockeye Suzy Fish Recalls Peppered Smoked Steelhead Cans

    Sockeye Suzys Fish LLC is recalling 13,281 cans of Peppered & Smoked Steelhead due to potential Clostridium botulinum contamination.

    Product
    Peppered & Smoked Steelhead, Sockeye Suzy Fish brand, metal can with a net weight of 6 oz. UPC 7 48252 67332 9
    Category
    Food
    Distribution
    2 states