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.

18526–18550 of 32106

  • SevereFDA (Drugs)·D-0212-2017·2016-12-28

    Virtus Recalls Hyoscyamine Sulfate Tablets Due to Content Uniformity Failures

    Virtus Pharmaceuticals is recalling Hyoscyamine Sulfate sublingual tablets because they failed content uniformity specifications, resulting in tablets that are either superpotent or subpotent.

    Product
    Hyoscyamine Sulfate, Sublingual Tablets, 0.125 mg, 100-count bottle, Rx only, Manufactured for: Virtus Pharmaceuticals OPCO II, LLC., Nashville, TN 37217, NDC 76439-309-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0209-2017·2016-12-28

    Colonia Care Pharmacy Recalls Injectable Drug Products Due to Sterility Concerns

    Colonia Care Pharmacy is recalling C-PAV/PHENTOL/ATROP/PGE1 injectable products due to lack of assurance of sterility. The recall affects products distributed in New Jersey and New York.

    Product
    C-PAV/PHENTOL/ATROP/PGE1, All strengths, All sizes, Rx only, Colonia Care Pharmacy, Colonia NJ 07067
    Category
    Drug
    Distribution
    2 states
  • SevereFDA (Food)·F-0776-2017·2016-12-28

    Wakefern Recalls Dipped Chocolate Chip Cookies Due to Metal Pieces

    Wakefern Food Corp. is recalling Dipped Chocolate Chip Cookies because they may contain metal pieces. The product was distributed in six states.

    Product
    Dipped Chocolate Chip Cookies Net Wt. 24 oz UPC 269954004995
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0227-2017·2016-12-28

    Meta Pharmacy Recalls Compounded Eye Drops Due to Sterility Concerns

    Meta Pharmacy Services is recalling Phenylephrine and Tropicamide compounded eye drops due to a lack of sterility assurance. The affected product was distributed to one consignee in Las Vegas.

    Product
    Phenylephrine 2.5% + Tropicamide 1% Compounded Eye Drops Solution, 5 mL bottles, Meta Pharmacy Services. NDC 99999-0106-99 Sterile compounded drug, Hospital/office use only, Not for resale Storage: ROOM TEMP
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Food)·F-0775-2017·2016-12-28

    Wakefern Recalls Kid's Rainbow Sprinkled Cookie Platter Due to Metal Pieces

    Wakefern Food Corp. is recalling Kid's Rainbow Sprinkled Cookie Platters because they may contain metal pieces. The product was distributed in six states.

    Product
    Kid's Rainbow Sprinkled Cookie Platter 4 lb 14 oz UPC 269935316994
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0746-2017·2016-12-28

    Midwest International Recalls Low Acid Canned Fish Without Registered Process

    Midwest International Corp is recalling low acid canned fish products that lack a registered manufacturer and scheduled process. The recall covers distribution in eight states.

    Product
    Qiejidingxiangyu, USA jiazhoufengwei, Fish, NET WT 4.2oz (120g)
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0785-2017·2016-12-28

    Wakefern Recalls 24-Count Candy Cookies Due to Metal Pieces

    Wakefern Food Corp. is recalling 24-Count Candy Cookies because they may contain metal pieces. The product was distributed in six states.

    Product
    24CT Candy Cookies Net Wt. 24oz UPC 208713004197
    Category
    Food
    Distribution
    6 states
  • SevereNHTSA·16V952000·2016-12-27

    Southwest Trailer-Mounted Generators Recalled for Tongue Separation Risk

    Southwest is recalling 2013-2016 QP25, QP35, and QP45/50 trailer-mounted generators because the trailer tongue may separate, creating a road hazard.

    Product
    SOUTHWEST — SOUTHWEST QP25 GENERATOR, QP35 GENERATOR, QP45/50 GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·121-2016·2016-12-23

    Gold Medal Packing Recalls Veal Products Due To E. Coli Contamination

    Gold Medal Packing is recalling approximately 4,607 pounds of boneless veal products due to possible E. coli O26 and O45 contamination. No illnesses have been reported.

    Product
    Copper City Meats, DBA Gold Medal Packing — Gold Medal Packing Inc. Recalls Veal Products Due To Possible E. Coli O26 and O45 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V949000·2016-12-23

    DRV Recalls 2016-2017 Elite and Mobile Suites Due to Brake Bolt Issue

    DRV Suites is recalling 2016-2017 Elite and Mobile Suites fifth wheel trailers because brake caliper bolts may loosen, potentially causing a loss of braking capability.

    Product
    DRV — DRV MOBILE SUITE, ELITE SUITES ALL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V929000·2016-12-23

    Mack Trucks Recalls Front Wheel Hubs on Pinnacle, Granite, and Titan Models

    Mack is recalling certain 2012-2017 trucks because front wheel hubs may fail, potentially causing loss of vehicle control or dropped parts.

    Product
    MACK — MACK PINNACLE (CXU), GRANITE (GU), PINNACLE (CHU), TITAN (TD)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V923000·2016-12-22

    Pierce Recalls 2015-2016 Dash CF Emergency Vehicles Due to Fire Risk

    Pierce Manufacturing is recalling 2015-2016 Dash CF emergency vehicles because a defective bracket may damage the starter motor, increasing the risk of a fire.

    Product
    PIERCE — PIERCE DASH CF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V925000·2016-12-22

    Ford Recalls 2016-2017 Vehicles for Turbocharger Oil Leak Fire Risk

    Ford is recalling specific 2016-2017 Taurus, Flex, MKT, and Explorer vehicles because improperly brazed turbocharger tubes may leak oil, increasing fire risk.

    Product
    FORD — FORD, LINCOLN FLEX, TAURUS, MKT, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·120-2016·2016-12-22

    Pork Rinds & Snacks Recalls Pork Skin Products Due to Salmonella Risk

    Pork Rinds & Snacks, LLC is recalling approximately 7,629 pounds of pork skin products that may be contaminated with Salmonella. The recall affects products shipped to five southeastern states.

    Product
    Pork Rinds & Snacks, LLC Recalls Pork Skin Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·16V926000·2016-12-22

    KME Predator Aerial Vehicles Recalled for Brake Defect

    KME is recalling certain Predator SS Aerial and Predator Aerial vehicles because rear brakes may engage without the pedal being pressed, increasing crash and fire risk.

    Product
    KME — KME PREDATOR AERIAL, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V928000·2016-12-22

    Volvo Recalls 2013-2017 Trucks Due to Brake System Contamination Risk

    Volvo is recalling certain 2013-2017 VNL, VNM, and 2017 VNX trucks because incorrect software may allow oil and water to contaminate the brake system, potentially affecting braking performance.

    Product
    VOLVO — VOLVO VNM, VNX, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V927000·2016-12-22

    Volvo Recalls 2017 Trucks Due to Front Wheel Hub Defect

    Volvo is recalling 2017 VHD, VNL, and VNM trucks because front wheel hubs may fail, risking loss of vehicle control.

    Product
    VOLVO — VOLVO VNM, VNL, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V947000·2016-12-22

    Chrysler Recalls 2009 Durango, Aspen, and 2010 RAM 3500 for Air Bag Defect

    Chrysler is recalling specific 2009 Dodge Durango, Chrysler Aspen, and 2010 RAM 3500 vehicles because the driver's air bag inflator may rupture during deployment, posing a risk of serious injury.

    Product
    DODGE — DODGE, CHRYSLER RAM 3500, ASPEN, DURANGO, redundant RAM 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0189-2017·2016-12-21

    Cantrell Drug Company Recalls Fentanyl Citrate Bags Due to Sterility Concerns

    Cantrell Drug Company is recalling Fentanyl Citrate bags due to a lack of assurance of sterility. The recall affects 2,545 bags distributed nationwide.

    Product
    Fentanyl Citrate 2,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 250 mL* Bag, Single-Dose Bag, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Road, AR 72207, NDC 52533-024-61
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0194-2017·2016-12-21

    Cantrell Drug Recalls Hydromorphone Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 2,509 single-dose Hydromorphone HCl syringes nationwide due to a lack of assurance of sterility.

    Product
    HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 mg/mL) Single-Dose Syringe, Rx Only, Cantrell Drug Co. 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-002-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0202-2017·2016-12-21

    Cantrell Drug Recalls Rocuronium Bromide Syringes Due to Sterility Concerns

    Cantrell Drug Company is recalling 5,067 syringes of Rocuronium Bromide 50 mg/5 mL injection solution nationwide due to a lack of assurance of sterility.

    Product
    Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) Single-Dose Syringe, Injection Solution For Slow IV Use, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-064-15
    Category
    Drug
    Distribution
    Distributed nationwide