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.

7951–7975 of 52968

  • HighFDA (Devices)·Z-2415-2024·2024-07-31

    Electrosurgical Generators Olympus ESG-410 May Fail to Power On

    Olympus is recalling 86 ESG-410 Electrosurgical Generators because they may fail to power on during use, potentially delaying treatment or prolonging surgery.

    Product
    ESG-410 Electrosurgical Generator- In conjunction with electrosurgical accessories intended for cutting and coagulation of tissue in open, laparoscopic , and endoscopic surgeries Model/Catalog Number: WA91307C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2435-2024·2024-07-31

    Perfusor Space syringe pump recalled for Cardinal Health syringe incompatibility

    B Braun is recalling Perfusor Space syringe pumps because manufacturing changes to Cardinal Health Monoject syringes may cause incompatibility, resulting in dosing errors or delayed treatment.

    Product
    Brand Name: Perfusor Space Product Name: Perfusor PCA Syringe Pump Model/Catalog Number: 8713080U Product Description: Perfusor¿ Space Syringe Pump, Infusion Pump, 1 each Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1494-2024·2024-07-31

    Signature Blue Canned Crab Recalled for Improper Temperature Control

    Pacific Shellfish, Inc. is recalling Signature Blue Swimming Crab Claw and Lump canned crab (lots #78821 and #788454) from California due to storage at temperatures above 40°F without ice as of July 1, 2024.

    Product
    Signature Blue Swimming Crab Claw and Lump 1lb can Tin Can, Lot # 78821 Expiration June 09th 2026, Lot # 788454 Expiration June 09th 2026
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2445-2024·2024-07-31

    LINK SymphoKnee Patella Sizing Template recalled due to incorrect markings

    LINK BIO CORP is recalling the LINK SymphoKnee Patella Sizing Template (Item Number 881-509/00, Lot C225066) because markings on two arms of the instrument were mixed up during manufacturing.

    Product
    LINK SymphoKnee Patella Sizing Template, Item Number 881-509/00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1490-2024·2024-07-31

    Organic Aussie Bites recalled for undeclared gluten content

    Best Express Foods is recalling Universal Bakery Organic Aussie Bites due to undeclared gluten. Products labeled as gluten-free were found to contain gluten above regulatory limits.

    Product
    Universal Bakery Organic Aussie Bites, 30 oz clamshell container USDA Organic Certified Gluten Free Rolled Oats, Dried Apricots, Flax Seeds, Sunflower Seeds, Honey, Coconut, Quinoa, Chia Seeds + More! INGREDIENTS: Organic Rolled Oats, Organic Oat Flour, Organic Invert Cane Sugar
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-2433-2024·2024-07-31

    Infusion Pump Syringe Compatibility Issue May Cause Overdose or Underdose

    B Braun is recalling Perfusor Space infusion pumps due to syringe compatibility issues with Cardinal Health Monoject syringes. The incompatibility may cause overdose, underdose, therapy delays, and alarm failures.

    Product
    Brand Name: Perfusor Space Product Name: Perfusor Space Infusion Pump System Model/Catalog Number: 8713030U Product Description: Perfusor Space Infusion Pump System, Infusion Pump, 1 each Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1515-2024·2024-07-31

    Glazed ceramic plates recalled for exceeding lead guidance levels

    Canadian Art Prints is recalling Indigenous Collection Signature Plates sets because the glazed ceramic plates may exceed FDA guidance levels for leachable lead. Consumers should stop using these plates immediately.

    Product
    UPC Code 772665860083, Stock code PLT008, Indigenous Collection Signature Plates set - Not Forgotten & Ancient Messages. Artist Maxine Noel on box and back of plates. Brand Indigenous Collection by CAP on box and back of plates. Not Forgotten is an image of a woman with indigeno
    Category
    Consumer Product
    Distribution
    18 states
  • HighFDA (Devices)·Z-2424-2024·2024-07-31

    BD Nano 2nd Gen Pen Needles recalled for post-expiration distribution

    Embecta Corp. is recalling BD Nano 2nd Gen Pen Needles that were distributed at or after their February 29, 2024 expiration date. Using expired needles cannot guarantee sterility and integrity.

    Product
    BD Nano 2nd Gen Pen Needles 32G X 4mm (5-count sample contained in Patient Counseling Sample Toolbox -Catalog 6484755/Lot Number: 3750144)-Sterile, single use devices designed for the parenteral administration of a drug from a cartridge contained in a drug pen injector Model/C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2427-2024·2024-07-31

    Medtronic A610 Clinician Programmer pocket adaptors limited to head-only MRI

    Medtronic recalled A610 Clinician Programmer software and pocket adaptors (Models 64001, 64002) due to MRI safety restrictions. Patients with these implants are limited to head-only MRI procedures.

    Product
    A610 Clinician Programmer (CP) Software Application (app) with the following versions: Version 2.0.x (2.0.4584, 2.0.4594, 2.0.4605, 2.0.4630, and 2.0.4648), Version 3.0.x (3.0.1057, 3.0.1062, 3.0.1081, and 3.0.1098), Version 4.0.x (4.0.1052). Includes the below product descripti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1516-2024·2024-07-31

    Indigenous Collection Signature Plates recalled for potential lead contamination

    Canadian Art Prints is recalling Indigenous Collection Signature Plates sets due to potential leachable lead exceeding FDA guidance levels. The affected sets were distributed across 18 US states.

    Product
    UPC 772665860106. PLT010. Indigenous Collection Signature Plates set - Dancing Bears & Three Bears on box and back of plate. Art by Dawn Oman. Brand Indigenous Collection by CAP on box and back of plate. The Dancing Bears is a scene with three dancing polar bears with a night s
    Category
    Consumer Product
    Distribution
    18 states
  • HighFDA (Food)·F-1613-2024·2024-07-31

    Bakery Cookie Recalled for Undeclared Peanut Allergen

    Shweetz Bakery-To-Go cookies are being recalled due to undeclared peanuts. The recall affects 11,070 cookies distributed across Pennsylvania, Maryland, Ohio, Virginia, and West Virginia.

    Product
    Shweetz Bakery-To-Go brand Peanut Butter Brownie Cheezecake Mashup Cookie Net Wt. 3 oz (85g) UPC: 759465005029. Individually packaged in a clear film wrap. 45 units per case. Frozen storage, thawed for retail sale.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2417-2024·2024-07-31

    Call station devices may fail to transmit emergency alarms to staff

    Securitas Healthcare's Arial Call Station (models CSK200 and CSK200MR) may fail to transmit alarms and experience premature battery depletion. The FDA recall affects 1,268 units distributed in the U.S. and Canada.

    Product
    Arial Call Station, Model Numbers CSK200 and CSK200MR, is a wireless, battery-operated call device installed inside resident living areas to allow immediate staff response.
    Category
    Medical Device
    Distribution
    9 states
  • HighFDA (Devices)·Z-2423-2024·2024-07-31

    Medtronic TourniKwik Tourniquet Set Recalled for Incorrect Component

    Medtronic is recalling 636 units of TourniKwik Tourniquet Sets due to incorrect components placed in four manufactured lots. Distribution includes the US states of Minnesota, Massachusetts, Utah, California, Florida, Japan, and Slovenia.

    Product
    TourniKwik Tourniquet Set (CFN 79012)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2428-2024·2024-07-31

    Beckman Coulter Clinical Reagent Recalled Due to Incorrect Lipemia Check Settings

    Beckman Coulter has recalled 13,565 units of IGM clinical reagent due to incorrect lipemia check settings that may produce false low results or report high results as normal. Affected units were distributed worldwide.

    Product
    Beckman Coulter, REF: OSR61173, IGM 4x14 mL R1, 4x11 mL R2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2418-2024·2024-07-31

    Wireless Nurse Call Station Recalled for Potential Alarm Communication Failure

    Arial Call Station wireless nurse call systems (models CSK200-1069 and CSK200-1069MR) are recalled due to risk of alarm communication failure and premature battery depletion. 77 units affected across multiple U.S. states.

    Product
    Arial Call Station, Model Numbers CSK200-1069 and CSK200-1069MR, is a wireless nurse call station.
    Category
    Medical Device
    Distribution
    13 states
  • HighFDA (Devices)·Z-2437-2024·2024-07-31

    Perfusor Space Syringe Pump Recalled for Monoject Syringe Incompatibility Risk

    B Braun's Perfusor Space infusion pump may be incompatible with Cardinal Health Monoject syringes affected by manufacturing changes, creating risks of overdose, underdose, and delayed therapy.

    Product
    Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Non-Wireless Model/Catalog Number: 8713032U Product Description: Perfusor Space Syringe Pump, Non-Wireless, Infusion Pump, 1 each Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V564000·2024-07-26

    Nova Bus window glazing may reduce the driver's visibility

    Nova Bus is recalling certain 2019-2023 LFS and LFS Artic buses because the glazing used on the glass windows may reduce the driver's visibility, failing FMVSS 205.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V561000·2024-07-26

    Hyundai Santa Fe floor wiring may chafe against the second row seat

    Hyundai is recalling certain 2024 Santa Fe and Santa Fe Hybrid vehicles because the main floor wiring harness may chafe and become damaged, affecting airbag deployment.

    Product
    HYUNDAI — HYUNDAI SANTA FE HYBRID, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V557000·2024-07-26

    BMW R 1300 GS starter motor relays may overheat

    BMW is recalling certain 2024 R 1300 GS motorcycles because the starter motor relay housing may have been manufactured incorrectly, resulting in a damaged relay that can overheat.

    Product
    BMW — BMW R 1300 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V563000·2024-07-26

    Forest River Cherokee Travel Trailer Recall for Microwave Fire Risk

    Forest River is recalling 2025 Cherokee CKT20-0G travel trailers because an incorrect screw in the microwave compartment can cause electrical arcing and fire.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24311·2024-07-25

    Lancaster Table & Seating Plastic Restaurant High Chairs Recalled for Fall Hazard

    Clark Associates is recalling about 27,140 Lancaster Table & Seating Standard Height Plastic Restaurant High Chairs because the T-bar at the front can become loose, fall, or break off during use, posing a fall hazard to children.

    Product
    Lancaster Table & Seating Standard Height Plastic Restaurant High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24312·2024-07-25

    2024 Kawasaki Mule PRO 1000 Utility Vehicles Recalled for Fire Hazard

    Kawasaki is recalling approximately 19,100 units of the 2024 Mule PRO 1000 utility vehicles due to improper combustion during engine start that can pose a fire hazard. Three fires have been reported with no injuries.

    Product
    2024 Kawasaki Mule PRO 1000 Off-Highway Utility Vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24313·2024-07-25

    Razor Icon Electric Scooters Recalled Due to Fall Hazard

    Razor is recalling about 7,300 Icon electric scooters because the downtube can separate from the floorboard during use, causing falls. The company has received 34 reports of downtube separation with two reported injuries.

    Product
    Razor Icon electric scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24316·2024-07-25

    Besrey Twins Strollers Recalled for Entrapment, Fall, and Choking Hazards

    Stiger Inc. is recalling about 3,045 Besrey Twins Strollers sold on Amazon due to entrapment, fall, and choking hazards that violate federal stroller safety regulations. Consumers should stop using the product immediately.

    Product
    Besrey Twins Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V560000·2024-07-25

    Nissan Ariya inverter software may shut down the EV system

    Nissan is recalling certain 2023 Ariya vehicles because the inverter software may misdiagnose an error and shut down the EV system, resulting in a loss of drive power.

    Product
    NISSAN — NISSAN ARIYA
    Category
    Vehicle
    Distribution
    Distributed nationwide