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.

21726–21750 of 32121

  • SevereNHTSA·15V619000·2015-10-02

    C&B Quality Trailer Works Recalls 2015-2016 Horse Trailers Due to Axle Weld Failure

    C&B Quality Trailer Works is recalling 79 model year 2015-2016 horse trailers because a weld on the torsion arm assembly may fail, allowing the wheel to separate from the trailer.

    Product
    C&B QUALITY TRAILER WORKS — C&B QUALITY TRAILER WORKS HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V617000·2015-10-01

    Daimler Trucks Recalls 2015-2016 Freightliner and Western Star Trucks

    Daimler Trucks is recalling 2015-2016 Freightliner and Western Star trucks because the transmission may lock or cause the vehicle to move backward unexpectedly.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 114SD, BUSINESS CLASS M2, 108SD, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16003·2015-10-01

    BSH Recalls Bosch, Gaggenau, Kenmore Elite, and Thermador Dishwashers for Fire Hazard

    BSH Home Appliances is recalling approximately 149,000 dishwashers because the power cords can overheat, posing a fire hazard. Consumers should stop using the units and contact the company for a free repair.

    Product
    Bosch, Gaggenau, Kenmore Elite and Thermador Dishwashers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V616000·2015-10-01

    Freightliner Trucks Recalled for Fifth Wheel Locking Mechanism Failure

    Daimler Trucks North America is recalling 2011-2014 Freightliner trucks because the fifth wheel locking mechanism may fail, risking trailer detachment.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA, BUSINESS CLASS M2, COLUMBIA GLIDER, CORONADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V618000·2015-10-01

    Ford Recalls 2016 Fusion and Lincoln MKZ for Fuel Tank Defect

    Ford is recalling 2016 Fusion and Lincoln MKZ vehicles because fuel tanks may have insufficient wall thickness, posing a fire risk if cracked in a crash.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3237-2015·2015-09-30

    Sam Mills Gluten Free Granola Bars Recalled for Undeclared Milk

    Sam MillsUSA LLC is recalling specific lots of Gluten Free Chocolate Chip Granola Bars because they contain undeclared milk, a major food allergen.

    Product
    Sam Mills Gluten Free Chocolate Chip Granola Bars with Dark Chocolate 5 bars/4.4oz Box (0.88oz each bar)
    Category
    Food
    Distribution
    35 states
  • SevereFDA (Drugs)·D-1824-2015·2015-09-30

    PharMEDium Recalls Morphine Sulfate IV Bags Due to Particulate Matter

    PharMEDium Services is recalling 100 bags of Morphine Sulfate IV solution because the sodium chloride used contained human hair.

    Product
    Morphine Sulfate, 1 mg per mL (250 mg per 250 mL), 250 mL total volume in a 250 mL LifeCare bag in Sodium Chloride 0.9%, IV Use Only, Rx only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-181-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V610000·2015-09-30

    Keystone Recalls 2016 Retreat and Residence Trailers for Weld Defect

    Keystone RV Company is recalling 2016 Retreat and Residence recreational trailers due to a potential insufficient weld on the rear mounting plate, which could increase crash risk.

    Product
    KEYSTONE — KEYSTONE RETREAT, RESIDENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1816-2015·2015-09-30

    Baxter Recalls Sodium Chloride Injection Bags Due to Sterility Concerns

    Baxter Healthcare is recalling 139,104 bags of 0.9% Sodium Chloride Injection due to a reported complaint of mold on the interior surface of the overpouch.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V613000·2015-09-30

    Daimler Recalls 2016 Freightliner Trucks Due to Steering Bolt Issue

    Daimler Trucks North America is recalling 10,843 model year 2016 Freightliner trucks because steering arm bolts may not be properly tightened, which could cause a loss of steering.

    Product
    FREIGHTLINER — FREIGHTLINER 114SD, 122SD, BUSINESS CLASS M2, COLUMBIA GLIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2799-2015·2015-09-30

    Regard Custom Surgical Pack Recalled for Chemical Contamination and Sterility Issues

    Resource Optimization & Innovation Llc is recalling 67 Regard Custom Surgical Packs due to potential chemical contamination and lack of sterility assurance.

    Product
    Regard Custom Surgical Pack, Item Number: 800208002; Sterile, CV0361B - CABG A&B. Used in cardiovascular surgical procedures.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-1828-2015·2015-09-30

    Pharmedium Recalls Phenylephrine Injection Bags Due to Particulate Matter

    Pharmedium Services is recalling 120 bags of Phenylephrine HCl injection due to the presence of human hair particulate matter.

    Product
    PHENYLephrine HCl, 10 mg added to 250 mL 0.9% Sodium Chloride Injection USP (40 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-149-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1827-2015·2015-09-30

    Pharmedium Phenylephrine Injection Recalled for Particulate Matter

    Pharmedium Services, LLC is recalling 48 bags of Phenylephrine HCl injection due to the presence of particulate matter, specifically human hair, in the product.

    Product
    PHENYLephrine HCl, 60 mg added to 250 mL 0.9% Sodium Chloride Injection USP (240 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-236-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1826-2015·2015-09-30

    Pharmedium Recalls Phenylephrine Injection Due to Human Hair Particulate Matter

    Pharmedium Services is recalling 84 bags of Phenylephrine HCl injection because the sodium chloride base contained human hair.

    Product
    PHENYLephrine HCl, 20 mg added to 250 mL 0.9% Sodium Chloride Injection USP (80 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-156-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1821-2015·2015-09-30

    Pharmedium Recalls Phenylephrine Injection Due to Human Hair Contamination

    Pharmedium Services, LLC is recalling specific lots of Phenylephrine HCl injection because the sodium chloride base used contained human hair.

    Product
    PHENYLephrine HCl, 50 mg added to 250 mL 0.9% Sodium Chloride Injection USP (200 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-171-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1825-2015·2015-09-30

    PharMEDium Recalls Fentanyl Citrate IV Bags Due to Particulate Matter

    PharMEDium Services, LLC is recalling 663 bags of Fentanyl Citrate IV solution because the sodium chloride used contained human hair.

    Product
    Fentanyl Citrate, 5 mcg per mL (1,250 mcg per 250 mL), 250 mL total volume in a 250 mL LifeCare bag in Sodium Chloride 0.9%, IV Use Only, Rx only, PharMEDium Services, LLC, 6100 Global Drive, Memphis, TN 36141, NDC# 61553-107-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1822-2015·2015-09-30

    Pharmedium Recalls Phenylephrine Injection Due to Human Hair Particulate Matter

    Pharmedium Services is recalling specific lots of Phenylephrine HCl injection due to the presence of human hair particulate matter.

    Product
    PHENYLephrine HCl, 40 mg added to 250 mL 0.9% Sodium Chloride Injection USP (160 mcg per mL), packaged in 250 ml bags, Rx only, PharMEDium Services, LLC, 12620 W. Airport Blvd., Sugar Land, TX 77478, NDC# 61553-169-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-3245-2015·2015-09-30

    Majopa Graviola Extract Recalled for Unapproved Drug Claims

    Majopa Industries is recalling 500 bottles of Graviola Extract sold in Puerto Rico because the label made unapproved drug claims, including cancer treatment.

    Product
    Label reads in part as: "GRAVIOLA EXTRACT***1 FL Oz (30 ml)*** ORIGINAL FORMULA***Manufactured by: Majopa Industries Corp.*** PRODUCT OF PUERTO RICO,USA". Drug claims in the product label are as follows: "Researchers have found that Extracts from Graviola leaves can produce…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2788-2015·2015-09-30

    Terumo Custom Cardiovascular Procedure Kits Recalled Due to Component Defect

    Terumo is recalling 30 custom cardiovascular procedure kits because they contain recalled Medivators HPH700 Hemoconcentrators.

    Product
    Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack with FX25RE P/N: 7928-03 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V608000·2015-09-29

    Ford Recalls 1998-2003 Windstar Minivans for Rear Axle Bracket Defect

    Ford is recalling 1998-2003 Windstar minivans because previously installed rear axle brackets may be misinstalled, potentially allowing the axle to fracture and increasing crash risk.

    Product
    FORD — FORD WINDSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V606000·2015-09-29

    Ford Recalls 2001-2008 Escape and Mariner for Transmission Shift Lever Defect

    Ford is recalling 2001-2008 Escape and Mercury Mariner vehicles with specific remanufactured transmissions because the shift lever bolt may not be tightened, risking vehicle rollaway.

    Product
    FORD — FORD, MERCURY ESCAPE, MARINER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V609000·2015-09-29

    GM Recalls 2016 Acadia, Traverse, Enclave for Wiper Motor Fire Risk

    General Motors is recalling 2016 Chevrolet Traverse, GMC Acadia, and Buick Enclave vehicles because the windshield wiper motor may overheat, increasing the risk of a fire.

    Product
    GMC — GMC, CHEVROLET, BUICK ACADIA, TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide