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.

25451–25475 of 32194

  • SevereFDA (Drugs)·D-1405-2014·2014-06-25

    John W Hollis Inc Recalls Pyridoxine HCl Injectable Due to Sterility Concerns

    John W Hollis Inc is recalling Pyridoxine HCl 100mg injectable products because they lack assurance of sterility. Consumers should stop using the product and contact their pharmacist.

    Product
    PYRIDOXINE HCL, Pyridoxine HCl 100mg, Also Contans: Benzyl Alcohol, Sodium Chloride, Water, Hydrochloric Acid, and/or Sodium Hydroxide, 30 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1391-2014·2014-06-25

    John W Hollis Recalls Polidocanol 5% Injection Due to Sterility Concerns

    John W Hollis Inc is recalling Polidocanol 5% Solution for Injection because the company cannot ensure the product is sterile.

    Product
    Polidocanol 5% Solution for Injection, each mL contains Polidocanol (Laureth 9) 50 mg, also contains Sterile Water for Injection, Ethyl Alcohol, Anhydrous Chlorobutanol, 50 mL Vial, JOHN HOLLIS Pharmacist Inc, Inc. 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1401-2014·2014-06-25

    John W Hollis Inc Recalls Compounded Injectable Drug Due to Sterility Concerns

    John W Hollis Inc is recalling a compounded injectable drug product due to a lack of assurance of sterility. The product is distributed nationwide.

    Product
    Papaverine HCl 30 mg, Phentolamine Mesylate 2 mg, Alprostadil 20 mcg, 10 mL, JOHN HOLLIS Pharmacist, Inc 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1389-2014·2014-06-25

    John W Hollis Inc Recalls Liver Derivative Complex Injection for Sterility Concerns

    John W Hollis Inc is recalling specific lots of Liver Derivative Complex for injection due to a lack of assurance of sterility in the compounded aseptically filled products.

    Product
    Liver Derivative Complex for injection, each mL contains: Liver Derivative Complex 25.5mg, also contains: Water for Injection, Phenol 0.5%, HCl or NaOH to adjust pH, 10 mL, Compounded by Prescription: JOHN HOLLIS Pharmacist Inc, 110 20th Avenue N, Nashville, TN 37203…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2024-2014·2014-06-25

    American Waffle Recalls Gluten-Free Blueberry Pancakes for Undeclared Milk

    American Waffle is voluntarily recalling one lot of liveGfree Gluten Free Blueberry Pancakes because the product contains undeclared milk.

    Product
    liveGfree Gluten Free Blueberry Pancakes NET WT 14.4 OZ, 12 pancakes Keep Frozen Distributed By Aldi, Inc., Batavia, IL 60510
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Drugs)·D-1397-2014·2014-06-25

    John W Hollis Inc Recalls Compounded Injectable Products Due to Sterility Concerns

    John W Hollis Inc is recalling specific lots of compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of sterility assurance.

    Product
    Papaverine HCl 30 mg, Phentolamine Mesylate 1 mg, Alprostadil 20 mcg, a) 5 mL and b) 10 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1403-2014·2014-06-25

    John W Hollis Inc Recalls Compounded Injectable Products Due to Sterility Concerns

    John W Hollis Inc is recalling compounded injectable products containing papaverine, phentolamine, and alprostadil due to a lack of sterility assurance.

    Product
    Papaverine HCl 30 mg, Phentolamine Mesylate 1 mg, Alprostadil 10 mcg, a) 5 mL and b) 10 mL, JOHN HOLLIS Pharmacist, Inc, 110 20th Avenue N, Nashville, TN 37203 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1406-2014·2014-06-25

    John W Hollis Recalls Polidocanol 1% Injection Due to Sterility Concerns

    John W Hollis Inc. is recalling Lot 2868 of Polidocanol 1% Solution for Injection because the company cannot ensure the product is sterile.

    Product
    Polidocanol 1% Solution for Injection, each mL contains Polidocanol (Laureth 9) 10 mg, also contains Sterile Water for Injection, Ethyl Alcohol, Anhydrous Chlorobutanol, 50 mL, JOHN HOLLIS Pharmacist, Inc. 110 B2 Avenue N, Nashville, TN 37203, 615-327-3234
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V363000·2014-06-24

    Suzuki Recalls 2004-2006 Verona Vehicles Due to Fire Risk

    Suzuki is recalling 2004-2006 Verona vehicles because heat in the daytime running light module could melt and cause a vehicle fire.

    Product
    SUZUKI — SUZUKI VERONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V364000·2014-06-24

    Vespa 946 Scooters Recalled for Fuel Line Leak Risk

    Piaggio is recalling 2013 Vespa 946 scooters because a fuel line may leak, potentially causing stalling or fire.

    Product
    VESPA — VESPA 946
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V358000·2014-06-23

    Gillig Recalls Low Floor Transit Buses Due to Oil Hose Fire Risk

    Gillig is recalling 2007-2014 Low Floor transit buses because an oil sampling hose may leak near hot exhaust components, increasing the risk of fire.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V355000·2014-06-23

    GM Recalls Vehicles for Ignition Switch Airbag Deployment Risk

    General Motors is recalling specific Buick, Cadillac, and Chevrolet models because the ignition switch may move out of the run position, potentially preventing airbag deployment and causing loss of power steering and braking.

    Product
    CADILLAC — CADILLAC, BUICK, CHEVROLET DEVILLE, LACROSSE, MONTE CARLO, DTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·038-2014·2014-06-21

    Wei-Chuan Recalls Pork Mini Buns Due to Undeclared Allergens

    Wei-Chuan USA is recalling Pork Mini Buns containing crab meat because the label failed to declare fish, shellfish, and egg allergens.

    Product
    Wei-Chuan USA, Inc. — California Firm Recalls Pork Mini Buns Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·14V346000·2014-06-20

    GM Recalls 2010-2014 Chevrolet Camaro for Ignition Key Defect

    General Motors is recalling 2010-2014 Chevrolet Camaros because the ignition key may be accidentally knocked out of the run position by the driver's knee, potentially disabling airbags and power steering.

    Product
    CHEVROLET — CHEVROLET CAMARO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V353000·2014-06-20

    Honda and Acura Vehicles Recalled for Takata Air Bag Inflator Defect

    Honda is recalling specific 2003-2006 vehicles sold or registered in California due to a Takata air bag inflator defect that could rupture during deployment.

    Product
    HONDA — HONDA, ACURA RIDGELINE, PILOT, RL, ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·036-2014·2014-06-19

    Thai Kitchen Chicken Pad Thai Recalled for Undeclared Soy Allergen

    Bellisio Foods is recalling Thai Kitchen Chicken Pad Thai frozen entrées because the packaging fails to list soy protein isolate, a known allergen.

    Product
    Bellisio Foods, Inc. — Ohio Firm Recalls Chicken Pad Thai Product Due to Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V338000·2014-06-19

    GM Recalls 2013-2014 Cadillac ATS and CTS for Transmission Cable Defect

    General Motors is recalling 2013-2014 Cadillac ATS and 2014 CTS vehicles because the transmission shift cable may detach, causing unintended movement or rollaway.

    Product
    CADILLAC — CADILLAC ATS, CTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V357000·2014-06-19

    Altec Aerial Trucks Recalled for Front Torsion Bar Weld Failure Risk

    Altec is recalling 258 aerial trucks because front torsion bar welds could fail, potentially causing vehicle instability and injury to the operator.

    Product
    ALTEC — ALTEC AT248F, AT237, AT3X-G, AT40-G
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V339000·2014-06-19

    GM Recalls 2015 Silverado and Sierra HD for Power Steering Hose Clamp Issue

    General Motors is recalling 2015 Chevrolet Silverado HD and GMC Sierra HD trucks because a power steering hose clamp may disconnect, potentially causing loss of steering and brake assist.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO HD, SIERRA HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-2018-2014·2014-06-18

    Poco Pac Salad Dressing Recalled for Undeclared Egg Allergen

    Diamond Crystal Brands is recalling Poco Pac Salad Dressing packets because they contain egg, which is not listed on the label.

    Product
    Poco Pac Salad Dressing, Distributed by Diamond Crystal Brands, Inc., Savannah, GA 31405, and packaged in single serve packets of 9 or 12 grams (g) of product. Product is packed as follows: 500 ct-9g (Product Code: 86251), 200ct-9g (Product Code: 86242) and 200 ct-12g (Product…
    Category
    Food
    Distribution
    19 states
  • SevereFDA (Food)·F-2019-2014·2014-06-18

    T.H. Seafood Recalls Frozen Rockfish Due to Missing Labeling Instructions

    T.H. Seafood Inc. is recalling approximately 2,000 lbs of raw, frozen rockfish because packaging labels failed to instruct consumers to keep thawed fish under refrigeration to control Clostridium botulinum.

    Product
    Raw, frozen, vacuum-packaged rock fish (portions, fillets, and whole fish, various sizes).
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1641-2014·2014-06-18

    Smiths Medical Recalls Mislabelled Portex Low Dead Space Connectors

    Smiths Medical ASD, Inc. is recalling one lot of Portex Low Dead Space Connectors with Sideport because 3.0mm devices were packaged and labeled as 3.5mm.

    Product
    Portex Low Dead Space Connector with Sideport, 3.5mm Product Usage: The connector is used to attach the endotracheal tube to the patient breathing circuit. The low dead space connector minimizes mechanical dead space and subsequent carbon dioxide rebreathing. The connector's…
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·14V335000·2014-06-18

    MCI Motor Coaches Recalled for Driveshaft Detachment Risk

    MCI is recalling specific 1993-1995 and 2006-2008 motor coaches because the driveshaft may detach, potentially causing loss of steering control and increasing crash risk.

    Product
    MCI — MCI 102DL3, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide