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.

18276–18300 of 29217

  • SevereFDA (Drugs)·D-1155-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Fentanyl Citrate Injection Syringes

    Cantrell Drug Company is recalling 235 syringes of fentanyl citrate injection because the drug was subpotent. The recall is voluntary and nationwide.

    Product
    fentaNYL CITRATE 25 mcg/mL in 5% DEXTROSE Injection, in 2 mL Syringe, Rx Only, Cantrell Drug Co., Little Rock AR --- UPC: 9999993301
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1615-2016·2016-07-13

    Norpac Organic Mixed Vegetables Recalled for Listeria Risk

    Norpac Foods is recalling 1,850 cases of Natural Directions Organic Mixed Vegetables due to potential Listeria monocytogenes contamination.

    Product
    Natural Directions Organic Mixed Vegetables, frozen, net wt. 12 oz. UPC 0 15400 19672 7
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Drugs)·D-1066-2016·2016-07-13

    QuVa Pharma Recalls Phenylephrine Syringes Due to Labeling Error

    QuVa Pharma is recalling 20 cases of Phenylephrine syringes because some units have incorrect strength labels on the protective overwrap.

    Product
    PHENYLephrine 1 mg/10 mL (100 mcg/mL) in 0.9% Sodium Chloride, 10 mL syringe, packaged in 24 syringes per case, Rx only, Healix Infusion Therapy Inc, 1075 W Park One Drive, Suite 200, Sugar Land Texas 77478, Product Code: 75901-1205-35.
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-1102-2016·2016-07-13

    Reliable Drug Recalls Triamcinolone Products Due to Processing Control Deficiencies

    Reliable Drug/Reliable Compounding Pharmacy is recalling all triamcinolone products compounded between March 2015 and March 2016 due to a lack of processing controls.

    Product
    All triamcinolone Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Drugs)·D-1164-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Midazolam Injection Syringes Nationwide

    Cantrell Drug Company is recalling 1,570 syringes of Midazolam HCl injection because the drug was found to be subpotent. The recall is voluntary and nationwide.

    Product
    MIDAZOLAM HCl in 0.9% Sodium Chloride Injection, 2 mg/2 mL (1 mg/mL), in 2 mL syringe, Rx only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-001-16 UPC: 0100352533001161
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1153-2016·2016-07-13

    Cantrell Recalls Subpotent Atropine Sulfate Injection Syringes Nationwide

    Cantrell Drug Company is recalling specific lots of Atropine Sulfate Injection Solution because the drug was found to be subpotent.

    Product
    Atropine Sulfate Injection Solution, 0.4 mg/1 mL (0.4 mg/mL), in a) 1 mL syringes and b) 2 mL syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- NDC 52533-010-45, UPC: 0100352533010453
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1613-2016·2016-07-13

    Sid Wainer Tart Shells Recalled for Undeclared Egg Allergen

    Sid Wainer and Son is recalling Domaine de Provence La Cucina Tart Shells because the product contains undeclared eggs, a major food allergen.

    Product
    Domaine de Provence La Cucina Tart Shells Produced Exclusively for Sid Wainer& Son, New Bedford, MA UPC Code: 708152149119 Item Number: 149110
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Drugs)·D-1092-2016·2016-07-13

    Reliable Compounding Pharmacy Recalls Minocycline Products Due to Processing Controls

    Reliable Compounding Pharmacy is recalling all minocycline products compounded between March 2015 and March 2016 due to a lack of processing controls.

    Product
    All minocycline Products, Rx Only, Compounded by RELIABLE DRUG/RELIABLE COMPOUNDING PHARMACY, 801 Irving St., SAN FRANCISCO, CA 94122.
    Category
    Drug
    Distribution
    3 states
  • SevereFDA (Food)·F-1658-2016·2016-07-13

    Kroger Stir Fry Starters Recalled for Possible Listeria Contamination

    The Pictsweet Company is recalling Kroger Stir Fry Starters because the onions included may be contaminated with Listeria monocytogenes.

    Product
    Kroger(R) VEGETABLES, broccoli, sugar snap peas, green bean carrots, celery, onions, mushrooms, & red bell peppers, STIR FRY STARTERS(R), NET WT 12 OZ (340g), UPC 11110 89775, DISTRIBUTED BY THE KROGER COMPANY, CINCINNATI, OH 45202
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1664-2016·2016-07-13

    Pictsweet Deluxe Stir-Fry Vegetables Recalled for Listeria Risk

    The Pictsweet Company is recalling Deluxe Stir-Fry Chinese Style Vegetables because they contain onions that may be contaminated with Listeria monocytogenes.

    Product
    PICTSWEET(R) Deluxe Stir-Fry Chinese Style Vegetables, Oriental Seasoning, NET WT 24 OZ (1 LB 8 OZ) 680g, UPC 70560 95689, DISTRIBUTED BY THE PICTSWEET COMPANY, BELLS, TN 38006
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1161-2016·2016-07-13

    Cantrell Drug Recalls Subpotent Lidocaine HCl Injection Syringes

    Cantrell Drug Company is recalling 450 syringes of Lidocaine HCl 1% injection due to subpotent drug levels. The recall is voluntary and nationwide.

    Product
    LIDocaine HCl 1% BUFFERED WITH SODIUM BICARBONATE Injection, packaged in 3 mL Syringes, Rx Only, Cantrell Drug Co., Little Rock, AR --- UPC: 9999992033
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V529000·2016-07-12

    Chrysler Recalls Vehicles for Transmission Wire Harness Defect

    Chrysler is recalling specific 2014-2016 vehicles because a transmission wire harness defect may cause the vehicle to unexpectedly shift to neutral, increasing crash risk.

    Product
    FIAT — FIAT, CHRYSLER, RAM 500X, 200, PROMASTER, CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V527000·2016-07-12

    Nissan Recalls 2012-2013 Infiniti M35 Hybrid for Engine Shutdown Risk

    Nissan is recalling 1,140 Infiniti M35 Hybrid vehicles because a system overheat may cause the engine to shut off while driving, increasing crash risk.

    Product
    INFINITI — INFINITI M35 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V525000·2016-07-11

    Heil Recalls 2014-2016 Trailers Due to Spring Brake Valve Defect

    Heil is recalling 2014-2016 trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    HEIL — HEIL FLATBED, PETROLEUM PULL TRAILER, DRY BULK TRAILER, CRUDE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V524000·2016-07-11

    Polar Tank Trailer Recalls 2014-2016 Models Due to Brake Delay

    Polar Tank Trailer is recalling 2014-2016 tank trailers because improperly machined brake valves may delay spring brake application, increasing the risk of the trailer rolling away.

    Product
    POLAR TANK — POLAR TANK MC 331 TANK TRAILER, DOT 412 TANK TRAILER, DOT 406 TANK TRAILER, NON-CODE TANK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E061000·2016-07-11

    Can-Am Spyder F3-T Recall for Passenger Seat Stability Issue

    Bombardier is recalling Can-Am Spyder F3-T motorcycles because an accessory passenger seat may fail to activate the vehicle stability system, increasing crash risk.

    Product
    CAN-AM — CAN-AM SPYDER F3-T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16215·2016-07-06

    Razor Recalls Hoverboards Due to Fire and Explosion Risk

    Razor USA is recalling about 28,000 Hovertrax hoverboards because their lithium-ion batteries can overheat, smoke, catch fire, or explode.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·16210·2016-07-06

    Hoverboard LLC Recalls Self-Balancing Scooters Due to Fire Hazard

    Hoverboard LLC is recalling Powerboard self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode. No injuries have been reported, but one instance of property damage occurred.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1574-2016·2016-07-06

    Reser's Deviled Egg Potato Salad Recalled for Listeria Risk

    Reser's Fine Foods is recalling Deviled Egg Potato Salad due to potential Listeria monocytogenes contamination from a recalled onion lot.

    Product
    Reser's Deviled Egg Potato Salad, Refrigerated, Retail package, Net wt. 3 lbs. UPC 0 71117 00480 9; Reser's Deviled Egg Potato Salad, Refrigerated, Foodservice product, net wt. 8 lbs. UPC 71117 00225; Safeway Deviled Egg Potato Salad, Refrigerated, Net wt. 16 oz. UPC 0…
    Category
    Food
    Distribution
    30 states