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.

11651–11675 of 29163

  • SevereFDA (Devices)·Z-2104-2019·2019-08-07

    Terumo Capiox NX19 Oxygenator Recalled for Non-Functioning Thermistor

    Terumo is recalling Capiox NX19 Oxygenators because they may contain a non-functioning arterial thermistor component.

    Product
    Terumo Capiox NX19 Oxygenator (West Orientation P/N:CXOT281 Exported only to Japan for inclusion into convenience kits that are sold only within the Japanese market
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1577-2019·2019-08-07

    Wise Pharmacy Recalls Compounded Papaverine Injectable Due to Processing Controls

    Wise Pharmacy is recalling 14 vials of compounded Papaverine/Phentolamine/Alprostadil/Atropine injectable due to a lack of processing controls.

    Product
    Papaverine/Phentolamine/Alprostadil/Atropine 30 mg/2 mg/50 mcg/0.15 mg/mL Injectable, 2.5 mL Vial, Rx only, Compounded by Wise Pharmacy, Littleton, CO 80123.
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1837-2019·2019-08-07

    Jubilant Cadista Recalls Drospirenone and Ethinyl Estradiol Tablets for Dissolution Failure

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Drospirenone and Ethinyl Estradiol Tablets because they failed dissolution specifications during stability testing.

    Product
    Drospirenone and Ethinyl Estradiol Tablets, USP, 3 mg/0.02 mg, packaged into a carton containing 3 blister cards each blister card contains 28-film coated, biconvex tablets, Rx Only, Manufactured by: Cyndea Pharma, S.L., Olvega (Soria), 42110 Spain, Distributed by: Jubilant…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V578000·2019-08-06

    Altec Recalls 2018-2019 Aerial Devices Due to Fastener Failure Risk

    Altec Industries is recalling 2018-2019 aerial devices because high-strength fasteners may fail, potentially causing the pedestal to separate from the turntable.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19766·2019-08-06

    BRP Recalls 2017-2018 Ski-Doo Snowmobiles Due to Fuel Leak and Fire Hazard

    BRP is expanding a recall for 2017-2018 Ski-Doo snowmobiles because the fuel delivery system can leak, posing a fire hazard. No injuries have been reported.

    Product
    2017 Ski Doo MXZ, Summit and Renegade snowmobiles and 2018 MXZ and Renegade snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·082-2019·2019-08-06

    Top Taste Recalls Pork and Chicken Dumplings Lacking USDA Inspection

    Top Taste Food Warehouse is recalling pork and chicken dumplings produced without USDA inspection. The products were shipped to New York wholesalers.

    Product
    Top Taste Food Inc. — Top Taste Food Warehouse Recalls Meat and Poultry Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V579000·2019-08-06

    BMW Recalls 2008-2012 Models for Blower Wiring Fire Risk

    BMW is recalling 2008-2012 128i, 135i, and 135is vehicles because blower-regulator wiring may overheat and cause a fire. Owners should contact dealers for a free inspection and replacement.

    Product
    BMW — BMW 135I, 128I, 135IS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V577000·2019-08-06

    KME Fire Trucks Recalled for Front Shock Separation Risk

    KME is recalling specific 2018-2019 Predator fire trucks because front shocks may separate, potentially causing a loss of power steering assist and increasing crash risk.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR TDA, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V573000·2019-08-05

    Altec Recalls 2017-2019 LS60 Aerial Devices for Stability Defects

    Altec Industries is recalling 2017-2019 LS60 Aerial Devices because they may not meet stability requirements, creating a risk of overturning and injury.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V572000·2019-08-02

    Mercedes-Benz Recalls 2020 GLE Models Due to Fuel Tank Weld Defect

    Mercedes-Benz is recalling 2020 GLE 350 and GLE 450 vehicles because an improper weld on the fuel filler pipe may cause a fuel leak, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V567000·2019-08-01

    Toyota Recalls 2019 Camry Vehicles for Air Bag Calibration Defect

    Toyota is recalling 2019 Camry vehicles because the occupant classification system may be improperly calibrated, potentially preventing front passenger air bags from deploying in a crash.

    Product
    TOYOTA — TOYOTA CAMRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V569000·2019-08-01

    Honda Recalls 2019 CR-V Vehicles for Fuel Tank Weld Defect

    Honda is recalling 2019 CR-V vehicles because an insufficient weld on the fuel tank may cause fuel leaks, increasing the risk of fire.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V568000·2019-08-01

    Winnebago Recalls 2018-2019 Fuse Motorhomes Due to Wheel Stud Defect

    Winnebago is recalling 2018-2019 Fuse motorhomes because wheel studs may be too long, preventing lug nuts from securing wheels properly and increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO FUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V566000·2019-08-01

    Thor Motor Coach Recalls 2019-2020 Omni and Magnitude Motorhomes

    Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because the battery tray may detach, causing the vehicle to stall.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH MAGNITUDE, OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1507-2019·2019-07-31

    Pharma-Natural Recalls Workvie Pain Roll-On for Manufacturing Violations

    Pharma-Natural Inc. is recalling Workvie Instant Pain Relieving Roll On due to current good manufacturing practice deviations, including lack of process and cleaning validation.

    Product
    Workvie Instant Pain Relieving Roll On (Lidocaine HCL 4% + Menthol 1% & Arnica), 2.5oz (71 g) roll on bottle, Exclusively Distributed by: Marketite, LLC., Coral Gables, FL 33134, NDC 72393-201-25.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1584-2019·2019-07-31

    Brand Castle Brownie Mix Recalled for Potential E. coli Contamination

    Brand Castle LLC is recalling Billion Dollar Brownie Mix due to potential E. coli contamination in flour. The product was distributed in ten states.

    Product
    Billion Dollar Brownie Mix, 28.3 oz glass jar, 6/case
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-1528-2019·2019-07-31

    Gordon Laboratories Recalls MONSEL'S Solution Due to Microbial Contamination

    Gordon Laboratories is recalling 277 boxes of MONSEL'S (Ferric Subsulfate) Solution due to microbial contamination and high iron content.

    Product
    MONSEL'S (Ferric Subsulfate) Solution, 8 mL amber glass bottle, packaged as one dozen bottles with applicators per box, Rx only, Gordon Laboratories, Upper Darby, PA 19082, NDC 10481-0112-8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1943-2019·2019-07-31

    Fruits Du Sud Golden Raisins Recalled for Undeclared Sulfites

    Frunut Global Commodities LLC is recalling Fruits Du Sud Golden Raisins because the product contains undeclared sulfites.

    Product
    Fruits Du Sud Golden Raisins, Golden Seedless Raisins, - Grade Medium Choice - Crop 2018 Net Weight 30LB (13.6KG), Production Date OCT 2018 Container Description: TRHU3994576
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1517-2019·2019-07-31

    Tris Pharma Recalls Hydrocodone and Chlorpheniramine Suspension Due to Potency Issues

    Tris Pharma is recalling 2,550 bottles of Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension due to high out-of-specification results for active ingredients and preservatives.

    Product
    HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX — HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX (HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1947-2019·2019-07-31

    Lisy Ground Cinnamon Recalled Due to High Lead Levels

    EL Chilar Huff is recalling Lisy Ground Cinnamon because a sample tested positive for high levels of lead.

    Product
    Lisy Ground Cinnamon Canela Molida NET WT./CONT. NETO 13 OZ (368g) and 2 OZ (57g)
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-1522-2019·2019-07-31

    Geritrex Recalls Gericare Diocto Liquid Stool Softener Due to Microbial Contamination Risk

    Geritrex, LLC is recalling 6,165 bottles of Gericare Diocto Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-403-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1622-2019·2019-07-31

    Eggland's Best Eggs Recalled for Temperature Control Failure

    C & S Wholesale Grocers is recalling Eggland's Best Grade A Large Eggs sold at two Target stores in New York due to a temperature control malfunction during transport.

    Product
    EGGLAND'S BEST GRADE A LARGE EGGS - 12CT UPC: 1514150349
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1525-2019·2019-07-31

    Geritrex Recalls Ritussin DM Due to Potential Microbial Contamination

    Geritrex, LLC is recalling Ritussin DM Double Strength cough syrup due to cGMP deviations that may result in microbial contamination.

    Product
    Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941
    Category
    Drug
    Distribution
    Distributed nationwide