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.

12651–12675 of 29171

  • SevereFDA (Drugs)·D-0748-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Fears & Nightmares Due to Microbial Contamination

    King Bio Inc. is recalling 96 bottles of Dr. King's SafeCare Rx Fears & Nightmares Mind & Body due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Fears & Nightmares Mind & Body, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955181026, NDC 57955-1811-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0923-2019·2019-03-20

    King Bio Inc. Recalls NET Remedies #7 Homeopathic Preparation Due to Microbial Contamination

    King Bio Inc. is recalling NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #7 Homeopathic Preparation, Oral Liquid, 57 mL, Manufacturer: King Bio Inc. U.S.A., Supplier: NET (Australia) Pty LTD 428 Hume Street, Toowoomba QLD 4350, Australia
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0816-2019·2019-03-20

    King Bio Recalls Calcium Metabolizer Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Calcium Metabolizer due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Calcium Metabolizer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955013129, NDC 57955-0131-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0582-2019·2019-03-20

    King Bio Homeopathic Leg Cramp Relief Recalled for Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Leg Cramp & Spasm Relief due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Leg Cramp & Spasm Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955543527, NDC 57955-6035-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0531-2019·2019-03-20

    King Bio Recalls Homeopathic Heart Regularity Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Heart Regularity due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Heart Regularity, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955506522, NDC 57955-5065-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0770-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Candida Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Candida bottles due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Candida, 8 fl. oz. (236 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955620686, NDC 57955-6207-8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0609-2019·2019-03-20

    King Bio Homeopathic Hair & Nails Formula Recalled for Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Hair & Nails Formula due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Hair & Nails Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504924, NDC 57955-5049-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0950-2019·2019-03-20

    King Bio Para Solve Homeopathic Liquid Recalled for Microbial Contamination

    King Bio Inc. is recalling NET Remedies #6 Para Solve Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #6 Para Solve Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4206-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0732-2019·2019-03-20

    King Bio Recalls Anti-Aging Cream Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955714729, NDC 57955-7148-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0557-2019·2019-03-20

    King Bio Recalls Homeopathic Arnica Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Advanced Arnica due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Advanced Arnica, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955598428, NDC 57955-5984-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·032-2019·2019-03-15

    Procesadora La Hacienda Recalls Corned Beef Due to Metal Contamination

    Procesadora La Hacienda is recalling approximately 4,940 pounds of ready-to-eat corned beef products that may contain pieces of metal. The products were distributed to institutions in Puerto Rico.

    Product
    Procesadora La Hacienda, Inc. — Procesadora La Hacienda, Inc. Recalls Beef Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereCPSC·19728·2019-03-14

    Kawasaki Recalls Mule Pro-MX Utility Vehicles Due to Fuel Leak Fire Hazard

    Kawasaki is recalling about 2,600 Mule Pro-MX off-highway utility vehicles because oil cooler hoses and fuel tank cap gaskets can fail, causing fuel leaks and fire hazards.

    Product
    Kawasaki Mule™ Pro-MX™ off-highway utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·031-2019·2019-03-14

    Breaded Chicken Patties Recalled for Possible Metal Contamination

    Productos La Aguadillana, Inc. is recalling breaded chicken patties that may contain pieces of metal. The products were shipped to institutions in Puerto Rico.

    Product
    Productos La Aguadillana, Inc. — Productos La Aguadillana, Inc. Recalls Breaded Chicken Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V204000·2019-03-14

    Hyundai Recalls 2013 Veloster Vehicles Due to Engine Software Defect

    Hyundai is recalling 2013 Veloster vehicles with 1.6-liter turbo engines because software may cause premature ignition, risking engine damage, fire, or stalling.

    Product
    HYUNDAI — HYUNDAI VELOSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V201000·2019-03-14

    Chrysler Recalls 2019 Jeep Wrangler and Ram 1500 for Steering Defect

    Chrysler is recalling 2019 Jeep Wrangler and Ram 1500 vehicles because improperly machined steering column stub shafts may break, potentially causing the steering wheel to detach.

    Product
    RAM — RAM, JEEP 1500, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19082·2019-03-14

    Tech Gear 5.7 Recalls Heated Socks Due to Fire and Burn Hazards

    Tech Gear 5.7 is recalling Mobile Warming Performance Heated Socks because the lithium-ion battery can overheat, melt, or ignite, posing fire and burn risks.

    Product
    Mobile Warming Performance Heated Socks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V200000·2019-03-14

    Thor Motor Coach Recalls 2018-2019 Aria and Palazzo Motorhomes

    Thor Motor Coach is recalling 2018-2019 Aria and 2019 Palazzo motorhomes because loose steering and tie rod arm bolts may separate, increasing crash risk.

    Product
    THOR — THOR ARIA, PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0987-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling six Maquet XS Flat Screen Monitor Holders because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, XS32 SPE, Configuration Part Number ARD22201040A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Devices)·Z-0989-2019·2019-03-13

    Maquet Flat Screen Monitor Holder Recalled for Grounding Non-Compliance

    Getinge US Sales LLC is recalling six Maquet XS Flat Screen Monitor Holders because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, PWD70+DF HD R XS32 K3 SPE, Configuration Part Number ARD268400150A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Food)·F-1154-2019·2019-03-13

    Ocean Beauty Seafoods Recalls Hot Smoked Salmon for Botulism Risk

    Ocean Beauty Seafoods is recalling Hot Smoked Salmon Variety Packs sold at Aldi due to potential Clostridium botulinum contamination from low salt content.

    Product
    Hot Smoked Salmon Variety Pack. ITEM # F3120SS9, Aldi ID# 51326. Each master case contains 12/4 oz. packs (4 packs of each flavor - Traditional, Cracked Black Pepper, and Cajun Flavored). Traditional, Hot Smoked Salmon, 4 oz. UPC 041498234881. Cajun Flavored, Hot Smoked…
    Category
    Food
    Distribution
    3 states
  • SevereUSDA FSIS·029-2019·2019-03-13

    Monogram Meat Snacks Recalls Pork Sausage Due to Product Tampering

    Monogram Meat Snacks is recalling approximately 191,928 pounds of ready-to-eat pork sausage products due to possible product contamination from tampering. No illnesses have been reported.

    Product
    Monogram Meat Snacks, LLC — Monogram Meat Snacks, LLC Recalls Pork Sausage Products Due to Possible Product Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0518-2019·2019-03-13

    Leiter's Recalls Cefuroxime Intravitreal Injection Due to Incorrect Formulation

    Leiter's Enterprises is recalling 569 vials of Cefuroxime 10 mg/mL intravitreal injection because the drug was compounded with sterile water instead of sterile 0.9% Sodium Chloride.

    Product
    Cefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use Only, Office Use Only, Leiter's (800) 292-6772- 17 Great Oaks Blvd., San Jose, CA 95119. NDC: 70360-007-35.
    Category
    Drug
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0990-2019·2019-03-13

    Maquet XS Flat Screen Monitor Holder Recalled for Grounding Defect

    Getinge is recalling four Maquet XS Flat Screen Monitor Holders in Arizona and Texas because they may not meet grounding requirements, posing a risk of electric shock.

    Product
    Maquet XS Flat Screen Monitor Holder, SAT XS32 12 SPE, Configuration Part Number ARD2SAT00130A Product Usage: This product is designed to support one or two medical grade flat screen(s) alone or in association with surgical lights.
    Category
    Medical Device
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0989-2019·2019-03-13

    Sunstone Organics Recalls Maeng Da Kratom Capsules Due to Salmonella Contamination

    Sunstone Organics is recalling Maeng Da Kratom capsules in 20, 60, and 150-count bottles because samples tested positive for Salmonella.

    Product
    Maeng Da Kratom, packaged in a) 20 count capsules (UPC 00859667007149), b) 60 count capsules (UPC 00859667007156), c) 150 count capsules (UPC 00859667007163) , Sunstone Organics Springfield, Oregon 97473, 541-972-3327.
    Category
    Drug
    Distribution
    4 states