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.

16576–16600 of 29206

  • SevereNHTSA·17V076000·2017-02-08

    Mercedes-Benz Recalls 2017 E-Class Models Due to Air Bag Defect

    Mercedes-Benz is recalling 2017 E300 and E43 AMG vehicles because the front passenger air bag may fail to deploy due to an incorrectly installed sensor.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300, AMG E43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1126-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled Due to Sterility Compromise

    Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising product sterility. The recall affects units distributed worldwide.

    Product
    Intact Disposable Wands (part of the Intact System) 777-110: 5 Pack 10mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V081000·2017-02-08

    Mercedes-Benz Recalls 2016 GL450 and GLE Models for Loose Suspension Bolt

    Mercedes-Benz is recalling 2016 GL450 and GLE models because a loose suspension bolt may cause improper wheel tracking, increasing the risk of a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE450, GL450, GLE350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1132-2017·2017-02-08

    Medtronic Intact Disposable Wands Recalled for Sterility Compromise

    Medtronic is recalling Intact Disposable Wands because the sterile barrier was breached, compromising sterility. The recall affects 499 units distributed worldwide.

    Product
    Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Pack 15mm Disposable Product Usage: The Intact Medical disposable wands are intended to provide breast tissue for histologic examination with partial or complete removal of an imaged abnormality and to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1373-2017·2017-02-08

    King's Pastry Recalls Frozen Mango Carnival Cake for Undeclared Hazelnut

    King's Pastry is recalling frozen Mango Carnival Cakes because the product contains undeclared hazelnut, a major food allergen.

    Product
    Mango Carnival Cake I(12" x 16"), 2.5 kg. Frozen Product Code: 10091 UPC: 1068596110913
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0464-2017·2017-02-08

    VistaPharm Recalls Oxycodone Hydrochloride Oral Solution Due to Water Contamination

    VistaPharm is recalling Oxycodone Hydrochloride Oral Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Oxycodone Hydrochloride Oral Solution, USP 5 mg/5 mL, a). 5 mL, 50 unit dose cups of 5 mL per case (NDC No. 66689-401-50), b). 500 mL, 12 bottles per case (NDC No. 66689-403-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1424-2017·2017-02-08

    Abbott Nutrition Recalls Nepro Mixed Berry Cans Due to Microbial Contamination

    Abbott Nutrition is recalling Nepro Mixed Berry 8oz cans due to off odor and taste caused by microbial contamination. The recall includes 362,400 units distributed in the US and several foreign territories.

    Product
    Nepro Mixed Berry, 8oz metal can
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0462-2017·2017-02-08

    VistaPharm Recalls Lactulose Solution Due to Potential Bacterial Contamination

    VistaPharm is recalling Lactulose Solution because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Lactulose Solution, USP 20 g/30 mL, 50 unit dose cups of 30 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-038-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0463-2017·2017-02-08

    VistaPharm Recalls Lactulose Solution Due to Potential Bacterial Contamination

    VistaPharm is recalling Lactulose Solution USP because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Lactulose Solution, USP 10 g/15 mL, 50 unit dose cups of 15 mL per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-039-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1409-2017·2017-02-08

    Houdini Inc. Recalls Vintners Path Cabernet Baskets Due to Salmonella Risk

    Houdini Inc. is recalling Vintners Path Cabernet Seasons Greetings Baskets due to potential Salmonella contamination. The product was distributed nationwide, including Puerto Rico.

    Product
    Vintners Path Cabernet Seasons Greetings Basket #763
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V079000·2017-02-08

    Mercedes-Benz Recalls 2016 GLE350 and GLS450 for Windshield Bonding Defect

    Mercedes-Benz is recalling 2016 GLE350 and GLS450 vehicles because insufficient windshield bonding may cause the glass to separate in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE350, GLS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0466-2017·2017-02-08

    VistaPharm Recalls Methadone Hydrochloride Due to Potential Bacterial Contamination

    VistaPharm is recalling Methadone Hydrochloride Oral Concentrate because purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    METHADONE HYDROCHLORIDE — METHADONE HYDROCHLORIDE (METHADONE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1368-2017·2017-02-08

    King's Pastry Tuxedo Bar Cake Recalled for Undeclared Hazelnut

    King's Pastry is recalling Tuxedo Bar Cakes because the product contains undeclared hazelnut, a tree nut allergen.

    Product
    Kings Pastry Tuxedo Bar Cake (12" x 4"), 1050 g Product Code: 10038 UPC: 685961100381
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0460-2017·2017-02-08

    VistaPharm Recalls Phenytoin Oral Suspension Due to Water Contamination

    VistaPharm is recalling Phenytoin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Phenytoin Oral Suspension, USP 100 mg/ 4 mL, 50 unit dose cups of 4 mL per case., Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-036-50.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0461-2017·2017-02-08

    VistaPharm Recalls Nystatin Oral Suspension Due to Water Contamination

    VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Nystatin Oral Suspension, USP 500,000 Units/5 mL, a). 50 unit dose cups of 5 mL per case (NDC No. 66689-037-50), b). 100 unit dose cups of 5 mL per case (NDC 66689-037-99), Rx only, Manufactured by VistaPharm, Largo, FL 33771.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1369-2017·2017-02-08

    King's Pastry Tuxedo Bar Cake Recalled for Undeclared Hazelnut

    King's Pastry is recalling Tuxedo Bar Cakes because the product contains undeclared hazelnut and/or tree nuts.

    Product
    Kings Pastry Tuxedo Bar Cake, (12" x 4") 1050g. Frozen Product Code: 10123 UPC: 6859611001234
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Drugs)·D-0457-2017·2017-02-08

    VistaPharm Recalls Nystatin Oral Suspension Due to Potential Water Contamination

    VistaPharm is recalling Nystatin Oral Suspension because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Nystatin Oral Suspension, USP 100,000 units per mL, a) 2 fl. oz. (60 mL), 24 bottles per case (NDC 66689-008-02), b) 16 fl. oz. (237 mL), 12 bottles per case (NDC 66689-008-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1384-2017·2017-02-08

    ASK Foods Recalls 3 Bean Medley Salad Due to Listeria Risk

    ASK Foods Inc is recalling 3 Bean Medley Salad products because they may be contaminated with Listeria monocytogenes.

    Product
    ASK Naturally Creative; 3 Bean Medley Salad; Net Wt. 10 lb. or Net Wt. 4 LB.
    Category
    Food
    Distribution
    2 states
  • SevereNHTSA·17V077000·2017-02-08

    Mercedes-Benz Recalls 2017 GLE and GLS Models for Center Console Defect

    Mercedes-Benz is recalling 2017 GLE and GLS models because the center console may unlatch in a crash, allowing objects to strike occupants.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS550, GLE550E, AMG GLS63, AMG GLE63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0467-2017·2017-02-08

    VistaPharm Recalls Methadone Hydrochloride Oral Concentrate Due to Water Contamination

    VistaPharm is recalling 3,354 bottles of Methadone Hydrochloride Oral Concentrate because the purified water used in manufacturing may have been contaminated with Burkholderia cepacia.

    Product
    Methadone Hydrochloride Oral Concentrate, USP 5 mg/5 mL C-II, 500 mL, 6 bottles per case, Rx only, Manufactured by VistaPharm, Largo, FL 33771, NDC No. 66689-711-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0449-2017·2017-02-08

    Dr. Reddy's Recalls Flucanazole Tablets for Dissolution Failures

    Dr. Reddy's Laboratories is recalling Flucanazole tablets because they failed dissolution and stability specifications.

    Product
    FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1422-2017·2017-02-08

    Abbott Nutrition Recalls Nepro Vanilla Due to Microbial Contamination

    Abbott Nutrition is recalling Nepro Vanilla 8oz cans due to off odor and taste caused by microbial contamination. The recall includes 332,088 units distributed in the US and several foreign territories.

    Product
    Nepro Vanilla , 8oz metal can
    Category
    Food
    Distribution
    0 states