The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

27026–27050 of 50462

  • HighNHTSA·18V800000·2018-11-13

    Volvo Recalls 2017-2019 Models Due to Telematics Software Error

    Volvo is recalling 2017-2019 models because a software error may prevent GPS location data from reaching emergency personnel during a crash.

    Product
    VOLVO — VOLVO XC90, V60, S90, XC60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V791000·2018-11-09

    Altec Cranes and Digger Derricks Recalled for Wiring Fire Risk

    Altec is recalling 2008-2018 cranes and digger derricks because undersized wiring may overheat and cause a fire. Owners should contact Altec for a free repair.

    Product
    ALTEC — ALTEC CRANE, DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V790000·2018-11-09

    Keystone Recalls 2018-2019 Raptor Trailers Due to Tire Rubbing

    Keystone is recalling 2018-2019 Raptor recreational trailers because tires may rub against the frame, potentially affecting handling and increasing crash risk.

    Product
    KEYSTONE — KEYSTONE RAPTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19714·2018-11-08

    Honda Recalls Pioneer 1000 Vehicles Due to Fire and Burn Hazards

    Honda is recalling approximately 56,000 Pioneer 1000 recreational off-highway vehicles because an incorrectly installed throttle body can ignite, posing fire and burn hazards.

    Product
    Recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19034·2018-11-08

    H.I.S. Recalls Girl's Clothing Sets with Lead-Containing Pendant Necklaces

    H.I.S. is recalling Self-Esteem brand girl's clothing sets because the included pendant necklaces contain lead levels exceeding federal bans. No injuries have been reported.

    Product
    Girl's clothing sets with pendant necklace
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V786000·2018-11-08

    Chrysler Recalls 2018 Jeep Wrangler Due to Door Latch Defect

    Chrysler is recalling 2018 Jeep Wrangler four-door vehicles because the right rear door latch may be misaligned, potentially preventing the door from latching properly.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19030·2018-11-08

    A. O. Smith Recalls 30-Gallon Gas Water Heaters Due to Fire Hazard

    A. O. Smith is recalling specific 30-gallon gas water heaters sold at Lowe's in California because the flame arrestor may fail, posing a fire risk.

    Product
    A. O. Smith 30 gallon gas water heaters with model number G6-UT3030N
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·19031·2018-11-08

    Lifetone Bedside Fire Alarm and Clock Recalled for Failure to Alert

    Lifetone Technology is recalling HLAC151 Bedside Fire Alarm and Clocks because the optional bed shaker may fail to operate during a fire emergency.

    Product
    Bedside Fire Alarm and Clock
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0178-2019·2018-11-07

    Pharm D Solutions Recalls Reck Injection Due to Sterility Concerns

    Pharm D Solutions is recalling 517 syringes of Reck Injection because the product lacks assurance of sterility. The recall covers lots distributed nationwide.

    Product
    Reck Injection, Pharm D Solutions, Houston, Texas --- NDC 69699-1459-50
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0352-2019·2018-11-07

    Trader Joe's Tomato & Basil Hummus Dip Recalled for Contamination Risk

    Bakkavor Foods USA is recalling Trader Joe's Tomato & Basil Hummus Dip due to potential Salmonella and Listeria monocytogenes contamination.

    Product
    Trader Joe's Tomato & Basil Hummus Dip, 7 oz. plastic container; Perishable, Keep Refrigerated. SKU 29153
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0367-2019·2018-11-07

    Baxter Recalls EXACTAMIX Empty EVA Bags Due to Potential Leaking

    Baxter Healthcare is recalling 281,350 units of EXACTAMIX Empty EVA Bags because they may leak after being used for compounding.

    Product
    EXACTAMIX Empty EVA Bags - 3000 mL Product Usage: A plastic container used to hold large-volume sterile solutions to be administered to a patient through an intravascular administration set.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0301-2019·2018-11-07

    Roche Diagnostics Recalls URISYS 1100 Urine Analyzers Due to Detection Limits

    Roche Diagnostics is recalling 14,398 URISYS 1100 Urine Analyzers because limits of detection for certain parameters were higher than listed, potentially causing false negative results.

    Product
    Roche Diagnostics URISYS 1100 Urine Analyzer Part Number: 03617556001 Product Usage: The URISYS 1100 Urine Analyzer is a reflectance photometer designed to automatically read and evaluate the results of Chemstrip 5 OB, Chemstrip 7, Chemstrip 10 MD, and Chemstrip 10 UA urine…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0121-2019·2018-11-07

    Sprayology Recalls Life Detoxer Homeopathic Oral Spray Due to CGMP Deviations

    Sprayology is recalling 1,473 bottles of Life Detoxer Homeopathic Oral Spray because manufacturing conditions could result in possible microbial contamination.

    Product
    Life Detoxer Homeopathic Oral Spray 1.38 fl. oz. (41 mL). Manufactured by Sprayology Gaithersburg, MD 20879NDC 61096-0023-1 and Tester NDC 61096-1023-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0349-2019·2018-11-07

    Melissa's Hatch Chile Clean Snax Recalled for Missing Peanut Allergen Labeling

    World Variety Produce is recalling Melissa's Hatch Chile Clean Snax because peanuts are listed in ingredients but not in the allergen information.

    Product
    Melissa's Hatch Chile Clean Snax, with Chia and flaxseed; 6.5 oz. plastic clamshell tub. Ingredients: Peanuts, Almonds, Cashews, Flaxseed, White Sesame Seeds, Evaporated Cane Juice, Green Match Chile Powder, Chia Seeds, Rice Syrup (Rice, Rice Milk Water), S=Honey, Sea, Salt.…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0106-2019·2018-11-07

    Sprayology Recalls Man Power Homeopathic Oral Spray Due to CGMP Deviations

    Sprayology is recalling Man Power Homeopathic Oral Spray because it was manufactured under conditions that could result in possible microbial contamination.

    Product
    Man Power, Homeopathic Oral Spray, 1.38 fl. oz (41ml), Manufactured for Sprayology Gaithersburg. MD 20879. NDC 61096-0025-1 and Tester NDC 61096-1025-1
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0355-2019·2018-11-07

    Caito Foods Recalls Southwest Stuffed Portabella Mushrooms Due to Contamination Risk

    Caito Foods LLC is recalling 220 units of Southwest Stuffed Portabella Mushrooms due to potential contamination with Listeria monocytogenes or Salmonella.

    Product
    SOUTHWEST STUFFED PORTABELLA MUSHROOM; 8oz. Black Foam Over-wrapped Trays; Keep Refrigerated; UPC 0081851202676
    Category
    Food
    Distribution
    7 states
  • HighFDA (Devices)·Z-0304-2019·2018-11-07

    Philips Brilliance 64 CT Scanner Software Recall for Misleading Reports

    Philips is recalling Brilliance 64 CT scanners with software version 4.1.6 because the Calcium Score report may display confusing information, potentially leading to patient mistreatment.

    Product
    Brilliance 64 (Model No. 728231), Software version 4.1.6 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0076-2019·2018-11-07

    Gourmet Specialties Recalls Fresh Basil for Potential Cyclospora Contamination

    Gourmet Specialties Inc. is recalling fresh basil from Mexico due to potential Cyclospora cayetanensis contamination. The product was distributed in California, Illinois, Nevada, and Arizona.

    Product
    Fresh Herb Basil 62/4oz., LB 2489, 135/5Bulk, 24/8oz., 12/10 bulk Product of Mexico
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0336-2019·2018-11-07

    Buddy's Kitchen Recalls Philly Steak Sandwiches Due to Listeria or Salmonella Risk

    Buddy's Kitchen is recalling Philly Steak Sandwiches due to potential Listeria or Salmonella contamination, linked to a McCain Foods recall.

    Product
    Philly Steak Sandwich, Item 06433. Net Weight 17.50 lbs. 56 - 5.00 oz. portions. Keep Frozen. For institutional use only. Buddy's Kitchen, Inc., Burnsville, MN 55337
    Category
    Food
    Distribution
    8 states