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.

41051–41075 of 50511

  • HighFDA (Food)·F-2034-2014·2014-06-25

    American Importing Recalls Cinnamon Crunch Granola Due to Undeclared Almonds

    American Importing Co, Inc is voluntarily recalling Cinnamon Crunch Granola because it may contain undeclared almonds, posing a risk to people with allergies.

    Product
    Product label: Amport Foods, Granola, Cinnamon Crunch, 22 oz (1 lb, 6 0z), UPC 0 71725 72511 0, Best BY 03-26-15, Ingredients: wheat flakes, oat flakes , brown sugar, sugar, coconut oil, coconut, wheat flour, cinnamon, honey, natural vanilla, sea salt. Allergy Information…
    Category
    Food
    Distribution
    5 states
  • HighCPSC·14737·2014-06-24

    Trane and American Standard Air Conditioners Recalled for Shock Hazard

    Trane recalls about 100,600 air conditioning units because defective ground screws may not provide sufficient grounding, posing a shock hazard.

    Product
    Trane XB300 and American Standard Silver SI Air Conditioning Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V360000·2014-06-23

    Palfleet Recalls 2009-2013 Ford Super Duty Trucks Due to Fire Risk

    Palfleet is recalling 2009-2013 Ford F-350, F-450, and F-550 Super Duty trucks modified with specific PTO assemblies because oil leaks may cause a fire.

    Product
    FORD — FORD F-450 SD, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V356000·2014-06-20

    Volvo VNL and VNM Trucks Recalled for Cruise Control Braking Defect

    Volvo is recalling 2011-2015 VNL and 2014-2015 VNM trucks because the active braking component of the enhanced cruise control can become disabled, increasing crash risk.

    Product
    VOLVO — VOLVO VNM, VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14211·2014-06-19

    Reebok Goalie Throat Collars Recalled for Laceration Hazard

    Reebok is recalling specific goalie throat collars because skate blades could penetrate the material, posing a risk of throat laceration. No injuries have been reported.

    Product
    Reebok TCPRE Senior and Junior Goalie Throat Collars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14212·2014-06-19

    Linear Recalls Personal Emergency Transmitters Due to Battery Signal Failure

    Linear LLC is recalling about 175,000 Personal Emergency Reporting System (PERS) transmitters because the batteries may fail to emit a low battery warning, leaving users unaware the device is not functioning.

    Product
    Personal Emergency Reporting System (PERS) Transmitters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V342000·2014-06-19

    GM Recalls 2014 Chevrolet Corvette Sport Seats for Air Bag Safety

    General Motors is recalling 2014 Chevrolet Corvettes with optional sport seats because they do not meet injury protection specifications for unbelted young children.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·037-2014·2014-06-19

    Dearborn Sausage Recalls Slab Bacon for Undeclared Soy Allergen

    Dearborn Sausage Company is recalling approximately 3,660 pounds of slab bacon because the product contains hydrolyzed soy protein, a known allergen, that is not declared on the label.

    Product
    Dearborn Sausage Company Inc — Michigan Firm Recalls Bacon Product Due To Misbranding and Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·14V352000·2014-06-19

    Terex Utility Vehicles Recalled for PTO Oil Leak Fire Risk

    James A. Kiley is recalling 2010-2013 Terex utility vehicles because oil may leak from the PTO pressure switch onto the exhaust, increasing fire risk.

    Product
    TEREX — TEREX LT40, T292, LT38
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1363-2014·2014-06-18

    Pantoprazole Sodium Tablets Recalled Due to Potential Mispackaging with Lorazepam

    Legacy Pharmaceutical Packaging is recalling Pantoprazole Sodium tablets because some cartons may contain Lorazepam tablets instead.

    Product
    Pantoprazole Sodium, Delayed-release tablets, USP, 40 mg tablets, 100 (10x10) unit dose packages, Manufactured by Dr. Reddy's Laboratories Limited, India and Distributed by Major Pharmaceuticals, Livonia, MI --- NDC 0904-6235-61
    Category
    Drug
    Distribution
    1 state
  • HighFDA (Devices)·Z-1756-2014·2014-06-18

    Stryker 3.0mm Round Fluted Bur Recalled for Missing Notches

    Stryker is recalling 285 sterile 3.0mm Round Fluted Bur Aggressive devices due to missing or partial notches. The defect may affect the device's compatibility with Elite Attachments.

    Product
    Stryker 3.0mm Round Fluted Bur Aggressive Sterile Product Usage: The devices are intended to be used to cut bone and bone related tissue during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT), orthopedic, and general surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14210·2014-06-18

    Brooks Furniture Recalls Glider Rockers Due to Fall Hazard

    Brooks Furniture is recalling glider rockers sold to Kaplan Early Learning because spindles can separate, posing a fall hazard. No injuries have been reported.

    Product
    Brooks Furniture Glider Rockers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2021-2014·2014-06-18

    T.H. Seafood Recalls Frozen Halibut Due to Missing Refrigeration Labeling

    T.H. Seafood Inc. is recalling raw, frozen halibut because the packaging lacks instructions to keep thawed fish under refrigeration, posing a Clostridium botulinum risk.

    Product
    Raw, frozen, vacuum-packaged halibut (portions, fillets, and whole fish of various sizes).
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1747-2014·2014-06-18

    Neo Metrics Recalls NovaGold Guidewires Due to Tip Uncoiling Risk

    Neo Metrics, Inc. is recalling NovaGold High Performance Guidewires because the tip may uncoil or detach more frequently than anticipated. No illnesses or injuries have been reported.

    Product
    Boston Scientific, NovaGold High Performance Guidewire, Rx only, Sterilized using ethylene oxide, UPN M00552010 and M00552000, Manufactured by NeoMetrics Inc, 2605 Fernbrook Lane Suite J, Plymouth, MN 55447. The NovaGold Guidewire is intended for use in selective cannulation…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1727-2014·2014-06-18

    Alere Triage D-Dimer Test Recalled for Incorrect Manufacturing

    Alere San Diego, Inc. is recalling 373 kits of the Alere Triage D-Dimer Test (Lot W53884B) because they may generate error codes or incorrect results.

    Product
    Alere Triage¿ D-Dimer Test PN 98100, Lot W53884B. The Alere Triage¿ D-Dimer Test is a fluorescence immunoassay to be used with the Alere Triage¿ Meters for the quantitative determination of cross-linked fibrin degradation products containing D-dimer in EDTA anticoagulated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1746-2014·2014-06-18

    Philips IntelliVue MX40 Wearable Patient Monitor Alarm Failure Recall

    Philips is recalling IntelliVue MX40 monitors because alarms may not resume after being paused, potentially delaying clinical response.

    Product
    IntelliVue MX40 Wearable Patient Monitor in use with the Philips IntelliVue Information Center iX (PIIC iX); 865350, 865351, 865352
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1744-2014·2014-06-18

    BioDerm Skin Wipes Recalled for Potential Bacterial Contamination

    BioDerm, Inc. is voluntarily recalling specific skin wipes used in male incontinence devices due to potential bacterial contamination from a contract manufacturer.

    Product
    BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). The recalled wipes are used on intact skin for applying skin protectant to the glands for control of male incontinence with an external, non-invasive and nonsterile device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1786-2014·2014-06-18

    Teleflex Recalls Taut Operative Cholangiogram Catheters Due to Missing Metal Support Tube

    Teleflex Medical is recalling 450 Taut Operative Cholangiogram Catheters because the metal support tube is missing. The recall covers units distributed in the US and Belgium.

    Product
    Taut Operative Cholangiogram Catheter, 4.5FR (1.5mm) x 76cm To facilitate the introduction of contrast media into the biliary ducts to obtain a cholangiogram during laparoscopic or open cholecystectomy.
    Category
    Medical Device
    Distribution
    18 states
  • HighFDA (Devices)·Z-1742-2014·2014-06-18

    BioDerm Skin Wipes Recalled for Potential Bacterial Contamination

    BioDerm, Inc. is voluntarily recalling skin-prep wipes used with external male catheters due to potential bacterial contamination.

    Product
    BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral collection chamber (Component: SKIN-PREP Protective wipes). The recalled wipes are used on intact skin for applying skin protectant to the glands for control of male incontinence with an external…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1740-2014·2014-06-18

    Ivoclar Vivadent Recalls Bluephase Style Light Probes Due to Broken Glass Fibers

    Ivoclar Vivadent is recalling 241 Bluephase style light probes because a stock check revealed broken glass fibers between the connector and the fiber bundle.

    Product
    bluephase style Light probe Pin-point 6>2 mm black REF # 636 241. The accessory is a pin point light probe, an accessory to a dental curing light Ultraviolet activator for polymerization for use during dental curing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1730-2014·2014-06-18

    Maquet PowerLED 700 Surgical Light Recall Due to Detaching Module

    Maquet is recalling PowerLED 700 surgical lights because plastic tabs may break, causing the ambient light module to partially detach.

    Product
    Maquet PowerLED 700. Product Usage; To provide illumination to the surgical area or the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide