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.

30826–30850 of 50502

  • HighNHTSA·17V561000·2017-09-12

    Highland Ridge Recalls 2018 Open Range 3X Trailers for Tire Labeling

    Highland Ridge RV is recalling 2018 Open Range 3X fifth wheel trailers because tire size labels may be incorrect, potentially leading to the installation of wrong-sized tires.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW OPEN RANGE 3X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17T015000·2017-09-11

    Trek Tire Recalls Dunlop GrandTrek PT3A Tires for Missing DOT Markings

    Trek Tire is recalling specific Dunlop GrandTrek PT3A tires manufactured in December 2016 because they lack complete DOT identification markings, which may increase crash risk.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V558000·2017-09-08

    Micro Bird Recalls 2016 G5 School Buses for Seat Safety Defect

    Micro Bird is recalling 25 units of 2016 G5 school buses because seat mounting studs may lack adequate padding, increasing injury risk in rear-end collisions.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17222·2017-09-08

    Nantucket Distributing Recalls Bimini Patio Set Chairs Due to Fall Hazard

    Nantucket Distributing is recalling Bimini patio set chairs because the fabric seat can tear, posing a fall hazard. Consumers should stop using the chairs and return them for a refund.

    Product
    Chairs sold with Bimini patio sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V555000·2017-09-07

    Thor Motor Coach Recalls 2014-2016 Motorhomes for Wiper Defect

    Thor Motor Coach is recalling 2014-2016 motorhomes because windshield wipers may fail due to incorrect installation, increasing crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR, THOR MOTOR TUSCANY XTE, DAYBREAK, ACE, MIRAMAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V556000·2017-09-07

    KZRV Recalls 2017-2018 Trailers Due to Missing Awning Light Fuse

    KZRV is recalling 2017-2018 Connect, Spree, and Sport Trek trailers because a missing fuse in the awning light circuit may cause wire overheating and fire.

    Product
    KZRV — KZRV CONNECT, SPREE, SPORT TREK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17E050000·2017-09-07

    J-Tech Recalls Icon Alliance Motorcycle Helmets Due to Chin Strap Defect

    J-Tech is recalling specific Icon Alliance motorcycle helmets because faulty stitching may allow the chin strap to separate, increasing injury risk in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17220·2017-09-07

    Studio Fun International Recalls Slap Bracelets Sold with Storybooks

    Studio Fun International is recalling slap bracelets sold with DreamWorks Trolls storybooks because the metal band can wear through the fabric, posing a laceration hazard.

    Product
    Bracelets sold with storybooks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3093-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3469-2017·2017-09-06

    Gold Medal Caramel Corn Mix Recalled for Undeclared Soy

    Gold Medal Products Co is recalling Corn Treats Concentrated Caramel Corn Mix because the label is missing an ingredient statement and does not declare soy.

    Product
    CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.
    Category
    Food
    Distribution
    18 states
  • HighFDA (Drugs)·D-1125-2017·2017-09-06

    Morton Grove Recalls Amoxicillin and Clavulanate Potassium Oral Suspension

    Morton Grove Pharmaceuticals is recalling 7,332 bottles of Amoxicillin and Clavulanate Potassium Oral Suspension due to a customer complaint of a blue nitrile glove fragment found in the product.

    Product
    Amoxicillin and Clavulanate Potassium for Oral Suspension, USP, 250/62.5 mg per 5 mL, 100 mL (when reconstituted) bottle, Rx Only, Manufactured By: Cipla Ltd. at Medispray Laboratories Pvt. Ltd., Kundaim Goa, India; Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3089-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US because a cooling system leak could cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3384-2017·2017-09-06

    Newark Nut Stores Recalls Bourbon Street Mix for Undeclared Cashews

    Newark Nut Stores is recalling Bourbon Street Mix because it contains undeclared cashews, a common allergen. The recall follows a customer complaint.

    Product
    Bourbon Street Mix, 157 25 lbs cases and 2,509 one (1) lb bags.
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-3096-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that can cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17218·2017-09-06

    Kawasaki Recalls Brute Force 300 ATVs Due to Fuel Leak Fire Hazard

    Kawasaki is recalling about 20,000 Brute Force 300 ATVs because the fuel tap or carburetor can leak fuel, posing a fire hazard. No injuries have been reported.

    Product
    Brute Force 300 all-terrain vehicles (ATVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3073-2017·2017-09-06

    Kentec Medical Recalls Pediatric Nasogastric Feeding Tubes Due to Radiopaque Stripe Defect

    Kentec Medical Inc is recalling specific lots of polyurethane ENFit nasogastric feeding tubes for pediatric and neonatal use because the radiopaque stripes are inadequately detectable.

    Product
    POLYURETHANE ENFit(R) AMERITUS NG FEEDING TUBE, REF Numbers: a) ENF-50P-40 b) ENF-50P-50 c) ENF-50P-80 d) ENF-60P-40 e) ENF-60P-50 f) ENF-60P-80 g) ENF-80P-40 h) ENF-80P-50 i) ENF-80P-80 j) ENF-100P-110 For pediatric and Neonatal Use, ENFit ENTERAL USE ONLY…
    Category
    Medical Device
    Distribution
    5 states
  • HighFDA (Devices)·Z-3099-2017·2017-09-06

    Siemens AXIOM Artis zee and Q/Q.zen X-ray Systems Recalled for Cooling Leak

    Siemens is recalling 986 AXIOM Artis zee and Q/Q.zen angiography systems in the US due to a cooling system leak that could cause equipment failure.

    Product
    Artis zee/zeego and Artis Q/Q.zen system, x-ray, angiographic AXIOM Artis zee and Q/Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to , pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3470-2017·2017-09-06

    Seven Sundays Muesli Recalled for Undeclared Almond Allergen

    Garden of Light Inc. is recalling Seven Sundays Vanilla Cherry Pecan Muesli because the product contains almonds but is labeled as containing only pecans.

    Product
    (a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch, UPC: 8-56088-00315-6 (b) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 2oz. cup UPC: 8-56088-00311-8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V549000·2017-09-06

    Keystone Recalls 2016-2018 Springdale and Summerland Trailers for Wiring Fire Risk

    Keystone RV Company is recalling 2016-2018 Springdale and Summerland recreational trailers because incorrectly connected wiring for electric stabilizer jacks can cause an electrical short and increase the risk of fire.

    Product
    KEYSTONE — KEYSTONE SUMMERLAND, SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3036-2017·2017-09-06

    NeuroLogica Recalls Samsung GU60A Digital X-ray Systems for Radiation Exposure

    NeuroLogica Corporation is recalling 87 Samsung GU60A digital X-ray systems because unintended areas are exposed to radiation during the Stitching function.

    Product
    Samsung GU60A system- Digital X-ray Imaging Systems are intended for use in generating radiographic images of human anatomy by a qualified/trained doctor or technician. This device is not intended for mammographic applications
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3480-2017·2017-09-06

    Schnucks Bakery German Chocolate Cakes Recalled for Unlabeled Pecans

    Schnucks Markets is recalling 13 German chocolate cakes mislabeled as Chocolate Iced Yellow Cake because they contain pecans not listed on the label.

    Product
    German chocolate cakes labeled as Schnucks Bakery Deluxe Petite Cake Chocolate Iced Yellow, Net Wt. 1 lb 1 oz (482 g), UPC 0 41218 31168 6
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-3079-2017·2017-09-06

    Recall of MEDLINE SIRUS Surgical Gowns Due to Inconsistent Sleeve Sealing

    Master & Frank (Pinghu) Co., Ltd. is recalling 2,160 units of MEDLINE SIRUS Surgical Gowns because inconsistent sleeve seam sealing may allow fluid to pass through.

    Product
    MEDLINE SIRUS Surgical Gown, Strong Protection, Poly-Reinforced, Breathable Film Sleeve, XXL-XLONG Sterile Single-Use Gown; Sold in kit with Sterile Gown/Hand Towel/CSR Wrap and boxes of 18 Gowns.
    Category
    Medical Device
    Distribution
    1 state