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.

25476–25500 of 32194

  • SevereFDA (Food)·F-2020-2014·2014-06-18

    T.H. Seafood Recalls Raw Frozen Black Cod Due to Labeling Error

    T.H. Seafood Inc. is recalling raw, frozen black cod because the packaging lacks instructions to keep the product frozen or refrigerated after thawing.

    Product
    Raw, frozen, vacuum-packaged black cod (portions, fillets, and whole fish, various sizes).
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2013-2014·2014-06-18

    United Bakery Recalls Parmesan Bread Sticks Due to Undeclared Egg Allergen

    United Bakery is recalling Parmesan Bread Sticks because egg is an ingredient in the cheese but is not declared on the label.

    Product
    United Bakery Grissini Parmesan Bread Sticks,; Made with Extra Virgin Olive Oil and Grano Padano Cheese; All Natural, Trans Fat Free; Packaged in 8 oz (227g) and 4.5 oz (128g) containers. Also packaged for Safeway - Safeway Select Parmesan Grissini Breadsticks, 8 oz.…
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1382-2014·2014-06-18

    Cubist Recalls CUBICIN Vials Due to Glass Shard Presence

    Cubist Pharmaceuticals is recalling 51,500 vials of CUBICIN (daptomycin) because a customer reported a glass shard in one vial.

    Product
    CUBICIN (daptomycin for injection), 500 mg single-use vial, Rx only, Manufactured for: Cubist Pharmaceuticals, Inc., Lexington, MA 02421, NDC 67919-011-01, UPC 3 67919-011-01 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1784-2014·2014-06-18

    Cordis EMPIRA RX PTCA Dilatation Catheter Recalled for Potential Bursting

    Cordis Corporation is recalling 80 units of EMPIRA RX PTCA Dilatation Catheters because they may exhibit radial versus axial tears if they burst during inflation.

    Product
    Cordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S For cardiovascular use.
    Category
    Medical Device
    Distribution
    9 states
  • SevereNHTSA·14V345000·2014-06-18

    GM Recalls 2014 Chevrolet Silverado and GMC Sierra for Floor Mat Defect

    General Motors is recalling specific 2014 Chevrolet Silverado and GMC Sierra trucks because optional floor mats may not be secured, potentially interfering with the accelerator pedal.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO, SIERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V336000·2014-06-18

    Dual-Tech Recalls Modified Ford F-550 Trucks Due to Fire Risk

    Dual-Tech is recalling 2009-2014 modified Ford F-550 trucks because oil leaks from a PTO switch may ignite the exhaust thermal blanket.

    Product
    FORD — FORD F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2022-2014·2014-06-18

    T.H. Seafood Recalls Raw Frozen Salmon Due to Labeling Defect

    T.H. Seafood Inc. is recalling raw, frozen, vacuum-packaged salmon because the labeling failed to instruct consumers to keep the product frozen or thawed under refrigeration to control Clostridium botulinum.

    Product
    Raw, frozen, vacuum-packaged salmon (portions, fillets, and whole fish, various sizes).
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1733-2014·2014-06-18

    Siemens Vista Air Compressor Recalled for Fire and Shock Hazards

    Siemens Healthcare Diagnostics is recalling four Vista Air Compressors because miswiring could cause a fire or electrical shock if powered up.

    Product
    Siemens Healthcare Diagnostics Vista Air Compressor. Vista AirCompressor replacement part: SMN 10706557 SKIT Air Compressor Assy, used on the Dimension Vista 500 and Dimension Vista 1500 systems. Siemens Healthcare Diagnostics Dimension Vista System is an in vitro…
    Category
    Medical Device
    Distribution
    3 states
  • SevereNHTSA·14V329000·2014-06-16

    MCI Motor Coaches Recalled for Interior Lighting Fire Risk

    Motor Coach Industries is recalling certain 2009-2011 MCI D4000, D4500, and 2010 D4505 motor coaches because excessive power draw from LED interior lights may cause heat buildup and fire.

    Product
    MCI — MCI D4000, D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V323000·2014-06-13

    Honda Recalls Acura ILX Vehicles for Headlight Fire Risk

    Honda is recalling certain 2013-2014 Acura ILX vehicles because excessive heat around the headlight bulb may cause smoke, melting, or fire, increasing crash risk.

    Product
    ACURA — ACURA ILX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V328000·2014-06-13

    Ford F-Series Trucks Recalled for PTO Switch Fire Risk

    Iowa Mold Tooling is recalling 2009-2014 Ford F-350, F-450, and F-550 SD trucks because a leaking PTO pressure switch may cause a fire.

    Product
    FORD — FORD F-450 SD, F-350 SD, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·035-2014·2014-06-13

    Vanee Foods Recalls Turkey Base Due to Undeclared Milk Allergen

    Vanee Foods is recalling approximately 3,156 pounds of turkey base misbranded as chicken base because it contains undeclared milk, a known allergen.

    Product
    Vanee Foods Company — Illinois Firm Recalls Turkey Base Product Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·14E030000·2014-06-13

    Meritor Recalls MFS12143ANN Axles Due to Weak Beam Spots

    Meritor is recalling specific MFS12143ANN non-drive steer axles because manufacturing errors may have created weak spots in the beam, increasing the risk of sudden axle failure and a crash.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V320000·2014-06-12

    BMW Recalls 2014 R 1200 RT Motorcycles for Rear Shock Absorber Defect

    BMW is recalling 950 model year 2014 R 1200 RT motorcycles because the rear shock absorber piston rod can break, causing loss of stability and increasing crash risk.

    Product
    BMW — BMW R 1200 RT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V322000·2014-06-12

    Winnebago Recalls 2014-2015 Motorhomes for Electrical Corrosion Risk

    Winnebago is recalling 2014-2015 Travato, Trend, and Itasca Viva motorhomes because water intrusion may cause electrical corrosion that disables safety features.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, ITASCA VIVA, TREND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V319000·2014-06-12

    Harley-Davidson Recalls 2014 Touring Motorcycles Due to Brake Line Pinch Risk

    Harley-Davidson is recalling 66,421 model year 2014 Touring and CVO Touring motorcycles because a front brake line may be pinched, potentially causing front wheel lock-up and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHR, FLHXSHRINE, FLHXS, FLHTKSHRINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V315000·2014-06-12

    GM Recalls 2012 Chevrolet Sonic Vehicles for Transmission Shaft Fracture Risk

    General Motors is recalling 21,567 model year 2012 Chevrolet Sonic vehicles because the transmission turbine shaft may fracture, potentially limiting speed or causing the vehicle to coast.

    Product
    CHEVROLET — CHEVROLET SONIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V325000·2014-06-12

    Hyundai Recalls 2015 Sonata Vehicles Due to Wiring Harness Defect

    Hyundai is recalling 2015 Sonata vehicles because a wiring harness defect may reduce power steering assist or prevent shifting from Park, increasing crash risk.

    Product
    HYUNDAI — HYUNDAI SONATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1357-2014·2014-06-11

    Losartan Potassium Tablets Recalled for Presence of Foreign Substance Debris

    Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because some bottles may contain debris swept up during cleaning.

    Product
    LOSARTAN POTASSIUM Tablets, USP, 50 mg, 30 count bottles, Rx only, Manufactured by Arrow Pharm (Malta) Ltd., Bizebbugia, Malta, Packaged by GSMS, Inc. Camarillo, CA --- NDC 60429-317-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1715-2014·2014-06-11

    Stryker NAV3i Platform Power Boxes Recalled for Missing Electrical Insulation

    Stryker is recalling 20 NAV3i Platform Power Boxes because they may lack electrical insulation on soldering joints, posing a shock hazard.

    Product
    The Stryker NAV3i Platform is a mobile cart platform consisting of the sub-components Stryker Nav3 Graphite Camera, SPC-3 Computer and IO-Tablet (touch screen) as well as the monitor, articulated arms and cart housing. This Navigation system is used in combination with surgical…
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Devices)·Z-1706-2014·2014-06-11

    GE Healthcare Recalls Kenex Ceiling Suspended Radiation Shields and Lamps

    GE Healthcare is recalling Kenex ceiling suspended radiation shields and surgical lamps due to improper installation. A reported incident involved a shield falling from the ceiling.

    Product
    Kenex Radiation Shield and surgical lamps installed with GE Healthcare Interventional, Surgery, CT and X-Ray Imaging systems. Kenex Suspension installed with Radiation shield and lamp with following model numbers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1719-2014·2014-06-11

    ConMed Recalls MACROLYTE Premie Dispersive Electrodes Due to Sparking and Burning

    ConMed Corporation is recalling MACROLYTE Premie Dispersive Electrodes due to confirmed complaints of sparking, no output, and burning at the cord set connection.

    Product
    MACROLYTE Premie Dispersive Electrode, REF 440-2400, CONMED CORPORATION. The device is applied to the patient during electrosurgical procedures to provide a path for RF current to leave the patient and return to the generator.
    Category
    Medical Device
    Distribution
    Distributed nationwide