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.

37401–37425 of 50506

  • HighCPSC·16704·2015-10-22

    L.L. Bean Recalls Hunting Knives with Sheath Due to Laceration Hazard

    L.L. Bean is recalling GTO Hunting Knives with Sheaths because the knife can cut through the sheath, posing a laceration hazard. No injuries have been reported.

    Product
    Hunting Knives with Sheath
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0115-2016·2015-10-21

    ViewRay MRIdian Radiation Therapy System Recalled for Unexpected Couch Movement

    ViewRay is recalling four MRIdian Radiation Therapy Systems because the patient couch may move unexpectedly if an encoder fails and the system is restarted.

    Product
    MRIdian¿ ViewRay¿ Radiation Therapy System, ViewRay¿ Is indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors, and conditions anywhere in the body when radiation treatment is indicated.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Drugs)·D-0013-2016·2015-10-21

    Sedalmex Pain Reliever Tablets Recalled for Potential Cephalosporin Contamination

    Midway Importing, Inc. is recalling Sedalmex pain reliever tablets due to potential cross-contamination with cephalosporin. Consumers should stop using the product and return it to the point of purchase.

    Product
    Sedalmex (Acetaminophen 500 mg with Caffeine 65 mg) Pain Reliever tablets, 20-count tablets in blisters per box, Manufactured in Mexico by: Merck, S.A. de C.V./, Imported & Distributed by Midway Importing, Inc., 1807 Brittmoore Rd, Houston, TX 77043, UPC: 1 88436 00017 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·16015·2015-10-21

    Innopower Recalls Hawk Climbing Sticks Due to Fall Hazard

    Innopower is recalling specific Hawk climbing sticks because the folding steps can bend or break, posing a fall hazard. Consumers should stop using the products and contact the company for a free replacement.

    Product
    Climbing Sticks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0008-2016·2015-10-21

    Old Time Candy Recalls French Burnt Peanuts Due to Allergen Mislabeling

    Old Time Candy is recalling 72 containers of French Burnt Peanuts because the packaging fails to list peanuts, sugar, artificial colors, and salt as ingredients.

    Product
    French Burnt Peanuts, NET WEIGHT 8 OZ (227g) Old Time Candy.com Distributed by Old Time Candy Company LaGrange, OH 44050 www.oldtimecandy.com Ingredients: Dextrose, Citric Acid, Calcium Stearate, Artificial Flavors, Artificial Colors***. May Contain Milk And Soy.
    Category
    Food
    Distribution
    29 states
  • HighFDA (Food)·F-0007-2016·2015-10-21

    Tastee Plain Caramel Apple Recall Due to Undeclared Peanut Allergen

    Tastee Apple Inc. is recalling Plain Caramel Apples because the product contains peanuts that are not listed on the label.

    Product
    TASTEE Plain Caramel Apple, www.tasteeapple.com NET WT. 3 OZ 85g 0 35266 00027 3 "THIS PRODUCT CONTAINS THE FOLLOWING ALLERGENS: MILK AND SOYBEAN***" TASTEE APPLE INC. NEWCOMERSTOWN, OH 43832
    Category
    Food
    Distribution
    9 states
  • HighFDA (Drugs)·D-0050-2016·2015-10-21

    Bedford Pharmacy Recalls P-P-P Injection Due to Sterility Concerns

    Bedford Pharmacy is recalling P-P-P (COBAL) 30-2-30/mL injections because of a lack of assurance of sterility. The product was distributed in New Hampshire and Massachusetts.

    Product
    P-P-P (COBAL) 30-2- 30/mL, Injection, Bedford Pharmacy, 209 Route 101, Bedford, NH 03110, (603) 472-3919
    Category
    Drug
    Distribution
    2 states
  • HighFDA (Devices)·Z-0119-2016·2015-10-21

    Zimmer Natural Nail CM Long Intramedullary Fixation Rods Recalled for Packaging Defects

    Zimmer GmbH is recalling 57,603 units of Natural Nail CM Long intramedullary fixation rods because compromised outer trays may lead to periprosthetic infection.

    Product
    Zimmer Natural Nail CM Long. Intramedullary Fixation Rod. The Zimmer Natural Nail System is intended for temporary fracture fixation and stabilization of the bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0121-2016·2015-10-21

    DJO Monode Shortwave Accessory Recalled for Overheating and Burning Insulation

    DJO, LLC is recalling Monode Shortwave Accessories due to overheating and burning of the wire insulation inside the applicator.

    Product
    Monode, Shortwave Accessory Model #: 02200002 Used in conjunction with the Intelect Shortwave Diathermy 100 and Intelect Shortwave Diathermy 400 units. For the clinical application of electromagnetic energy in the radio frequency of 27.12 megahertz to generate deep heat…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0123-2016·2015-10-21

    Clinical Innovations Recalls Ebb Complete Tamponade System Due to Balloon Leak Risk

    Clinical Innovations, LLC is voluntarily recalling the Ebb Complete Tamponade System due to a potential balloon leak that may prevent the device from delivering therapy when needed.

    Product
    The Ebb Complete Tamponade System, model #CTS-1000 and Code #OQY. Intended for use in providing temporary control or reduction of postpartum uterine bleeding.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16010·2015-10-20

    Turtle Beach Recalls XO FOUR Stealth Gaming Headsets Due to Mold Risk

    Turtle Beach is recalling about 59,500 XO FOUR Stealth gaming headsets because mold spores were found on the units, posing a risk of respiratory or other infections.

    Product
    Ear Force® XO FOUR Stealth gaming headset
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16012·2015-10-20

    Big Game Recalls Climbing Tree Stands Due to Fall Hazard

    Big Game is recalling about 12,200 climbing tree stands because the cable assembly can release, posing a fall hazard. One injury report has been received.

    Product
    Climbing tree stands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V681000·2015-10-20

    Nissan and Infiniti Recall Vehicles Due to Passenger Air Bag Defect

    Nissan is recalling specific 2013-2015 models because a faulty sensor may prevent the passenger air bag from deploying in a crash.

    Product
    INFINITI — INFINITI, NISSAN QX60, PATHFINDER, JX35, ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V670000·2015-10-19

    Utilimaster Walk-In Van Recall for Incorrect Tire Placard Cargo Capacity

    Spartan Motors USA is recalling 2014-2015 Utilimaster Walk-In Vans because the tire placard may display incorrect cargo capacity information, potentially leading to vehicle overload.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V672000·2015-10-19

    Volvo Recalls 2016 VN Trucks for Engine Stalling Risk

    Volvo is recalling 2016 VN trucks because a faulty engine control module may cause the engine to stall without warning, increasing crash risk.

    Product
    VOLVO — VOLVO VN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V664000·2015-10-16

    Winnebago and Itasca Motorhomes Recalled for Transmission Shift Cable Defect

    Winnebago is recalling 2015-2016 Brave, Sightseer, Vista, Adventurer, and Itasca models because they can shift out of park without brakes applied.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA SIGHTSEER, VISTA, BRAVE, ADVENTURER
    Category
    Vehicle
    Distribution
    Distributed nationwide