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.

22526–22550 of 32171

  • SevereFDA (Devices)·Z-2046-2015·2015-07-15

    Biomet Recalls A.L.P.S. Foot Locking Calcaneus Plates Due to Thread Defects

    Biomet is recalling 75 A.L.P.S. Foot Locking Calcaneus Plates because thread defects may cause screws to back out or shear, potentially requiring revision surgery.

    Product
    A.L.P.S. Foot Locking Calcaneus Plate,Small-Right. Provides the orthopaedic surgeon a means of bone fixation and helps generally in the management of fractures and reconstructive surgeries.
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Food)·F-2818-2015·2015-07-15

    Popcorn Factory Recalls Dill Pickle Popcorn Due to Undeclared Milk Allergen

    The Popcorn Factory is recalling Dill Pickle Lite Works Popcorn because it contains milk, an allergen not declared on the label.

    Product
    Dill Pickle Lite Works Popcorn , lot number 15111, packaged in a 4 oz foil white bag with black and green lettering.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-2788-2015·2015-07-15

    Kerry Foods Recalls Nondairy Creamer Due to Potential Metal Fragments

    Kerry Foods is voluntarily recalling specific lots of nondairy creamer produced in May 2015 due to the potential presence of small metal pieces from a broken production screen.

    Product
    Kraft French Vanilla, Creamer, Non-Dairy Creamer, Net WT/Contenido Neto 35.3 oz (1 kg) SKU 2100002971. Publix, Nondairy, FrenchVanilla, Naturally and Artificially Flavored Coffee Creamer, Net Wt 15 oz (425 g), SKU 4141501625.
    Category
    Food
    Distribution
    3 states
  • SevereCPSC·15182·2015-07-15

    Cooper Lighting Recalls Fluorescent Fixtures Due to Fire Hazard

    Cooper Lighting is recalling about 1.62 million fluorescent fixtures because the sockets can overheat, arc, and melt, posing a fire hazard.

    Product
    Cooper Lighting, Portfolio and Utilitech fluorescent lighting fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1950-2015·2015-07-15

    Shiley Neonatal and Pediatric Tracheostomy Tubes Recalled for Breathing Difficulties

    FDA is recalling Shiley Neonatal and Pediatric Tracheostomy Tubes because patients reported discomfort and breathing difficulties after switching to these products.

    Product
    Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube, Cuffless. Model Numbers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2841-2015·2015-07-15

    Brown Betty Coconut Milk Powder Mix Recalled for Undeclared Milk Allergen

    Bedessee Imports is recalling Brown Betty Coconut Milk Powder Mix because it contains sodium caseinate but lacks a milk declaration.

    Product
    Bedessee Brown Betty BRAND COCONUT MILK Powder Mix, NET WT: 1) 1.76 OZ (50 g) and 2) 10.6 OZ. IMPORTED BY BEDESSEE IMPORTS LTD. Brooklyn, NY USA 11208. PRODUCT OF VIETNAM.
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Drugs)·D-1089-2015·2015-07-15

    Teva Recalls Adrucil Fluorouracil Injection Due to Particulate Matter

    Teva Pharmaceuticals is recalling Adrucil (fluorouracil injection) vials due to the presence of black particulate matter, including silicone rubber and drug crystals.

    Product
    Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For Intravenous Use Only, Rx Only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-3019-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E058000·2015-07-14

    Agility Fuel Systems Recalls CNG Fuel Systems Due to Pressure Relief Defect

    Agility Fuel Systems is recalling certain compressed natural gas (CNG) fuel systems because pressure relief devices may fail to vent pressure, increasing the risk of tank explosion, fire, and injury.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15E059000·2015-07-14

    Emcara Pressure Relief Devices Recalled for CNG Tank Explosion Risk

    Emcara is recalling specific Pressure Relief Devices (PRDs) that may fail to vent pressure, potentially causing CNG tank explosions, fire, and injury.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15T011000·2015-07-13

    Hercules Recalls All Trac A/T Tires Due to Tread Separation Risk

    Hercules Tire & Rubber Company is recalling approximately 90,000 All Trac A/T tires because the tread may separate, increasing the risk of a vehicle crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·096-2015·2015-07-12

    Barber Foods Recalls Stuffed Chicken Products Due To Salmonella Risk

    Barber Foods is recalling approximately 1.7 million pounds of frozen, raw stuffed chicken products that may be contaminated with Salmonella Enteritidis.

    Product
    AdvancePierre Foods, Inc. — Barber Foods Recalls Stuffed Chicken Products Due To Possible Salmonella Enteritidis Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V443000·2015-07-10

    Autocar Recalls 2015-2016 Xpeditor Vehicles Due to HVAC Fire Risk

    Autocar is recalling 1,042 model year 2015-2016 Xpeditor vehicles because the defrost mode door actuators in the HVAC units may overheat, increasing the risk of a fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V442000·2015-07-10

    GM Recalls 2014-2015 Chevrolet Cruze and Volt for Steering Defect

    General Motors is recalling specific 2014-2015 Chevrolet Cruze and 2015 Chevrolet Volt vehicles because the inner tie rod may not be tightened correctly, which could cause the tie rod to separate from the steering gear.

    Product
    CHEVROLET — CHEVROLET CRUZE, VOLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V444000·2015-07-10

    Dodge Challenger Recall: Driver Air Bag Inflator Rupture Risk

    Chrysler is recalling 2008-2010 Dodge Challengers because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.

    Product
    DODGE — DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V440000·2015-07-10

    Wilson Recalls 2006-2015 Grain Trailers Due to Kingpin Weld Failure Risk

    Wilson Trailer Company is recalling 2006-2015 Grain trailers because welds on the kingpin assembly may fail, potentially causing the trailer to detach from the tractor.

    Product
    WILSON — WILSON GRAIN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15178·2015-07-09

    Hearth & Home Technologies Recalls Gas Fireplaces Due to Fire Hazard

    Hearth & Home Technologies is recalling about 2,500 indoor gas fireplaces because the back of the firebox can bow out, posing a fire hazard.

    Product
    Heat-N-Glo® and Heatilator® Corner Unit Series indoor gas fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1496-2015·2015-07-08

    Snoqualmie Blackberry Sorbet Recalled for Potential Listeria Contamination

    Snoqualmie Gourmet Ice Cream is recalling Blackberry Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 1.5 and 3 gallon tubs.

    Product
    Blackberry Sorbet, sold under Snoqualmie brand. Product is sold in 1.5 and 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1506-2015·2015-07-08

    Snoqualmie Cranberry Raspberry Sorbet Recalled for Listeria Risk

    Snoqualmie Gourmet Ice Cream is recalling Cranberry Raspberry Sorbet due to potential Listeria monocytogenes contamination.

    Product
    Cranberry Raspberry Sorbet, sold under Snoqualmie brand. Product is sold in 1 gallon plastic trays; 1.5 and 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1178-2015·2015-07-08

    Lincare Recalls Hydrocodone IV Bags Due to Sterility Concerns

    Lincare, Inc. is recalling specific lots of Hydromorphone HCl IV bags because the sterility of the product is not assured.

    Product
    HYDROmorphone HCl PF, HYDROMORPHONE HCL 1000mg /NS 500mL, Qty: 1 500 mL Bag, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1195-2015·2015-07-08

    Lincare Recalls Gentamicin Syringes Due to Sterility Concerns

    Lincare, Inc. is recalling Gentamicin 14.4 mg syringes because the sterility of the product is not assured. The recall affects 2 syringes distributed in Arkansas.

    Product
    GENTAMICIN 14.4 mg / NS 30 mL SYRINGE, Packaged in 30 mL Syringes, Rx Only. Compounded by: United Medical IV Center (Little Rock) 1527 South Bowman Rd. Ste. D Little Rock, AR 72211-4200.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Food)·F-1526-2015·2015-07-08

    Snoqualmie Orange Pomegranate Sorbet Recalled for Listeria Risk

    Snoqualmie Gourmet Ice Cream is recalling Orange Pomegranate Sorbet due to potential Listeria monocytogenes contamination.

    Product
    Orange Pomegranate Sorbet, sold under Snoqualmie brand. Product is sold in 1.5 and 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1531-2015·2015-07-08

    Snoqualmie Bartlett Pear Sorbet Recalled for Listeria Contamination Risk

    Snoqualmie Gourmet Ice Cream is recalling Bartlett Pear Sorbet due to potential Listeria monocytogenes contamination. The product was distributed nationwide in 1.5 and 3 gallon tubs.

    Product
    Pear (Bartlett Pear) Sorbet, sold under Snoqualmie brand. Product is sold in 1.5 and 3 gallon plastic tubs. No UPC.
    Category
    Food
    Distribution
    Distributed nationwide