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.

28201–28225 of 50488

  • HighFDA (Devices)·Z-2560-2018·2018-08-08

    Galt Medical Recalls Centesis Catheters Due to Bacterial Endotoxin Contamination

    Galt Medical Corporation is recalling specific lots of Drainer and Centeze Centesis Catheters because they may contain unsafe levels of bacterial endotoxins.

    Product
    1) Drainer Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-001-05, b) DRC-001-06, c) DRC-001-15, 2) Centeze Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-002-02, b) DRC-002-05, c) DRC-002-06, d) DRC-002-08,
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-2580-2018·2018-08-08

    GE Healthcare Recalls CT Systems With Potential Electrical Wiring Defect

    GE Healthcare is recalling 42 Discovery MI CT systems installed with a specific electrical panel that may not be properly wired to the UPS.

    Product
    Discovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2475-2018·2018-08-08

    Siemens SOMATOM Perspective 16 CT Scanner Recalled for Software Issue

    Siemens Medical Solutions USA is recalling SOMATOM Perspective 16 CT scanners due to a software issue that may cause unnecessary radiation exposure.

    Product
    SOMATOM Perspective 16 (Model 10891666)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1900-2018·2018-08-08

    Griffith Labs Recalls Seasoned Crouton Seasoning Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling 183 bags of Seasoned Crouton Seasoning N5 due to the potential presence of Salmonella from a recalled whey ingredient.

    Product
    Seasoned Crouton Seasoning N5 50 pound bag Item 1000011143
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1774-2018·2018-08-08

    Mondelez Recalls Ritz Bits Cheese Big Bags Due to Salmonella Risk

    Mondelez Global is recalling Ritz Bits Cheese Big Bags because a supplier's whey powder ingredient may contain Salmonella.

    Product
    RITZ BITS CHEESE BIG BAG 3 Oz, Pouch Retail: 12 per case Foodservice: 36 per case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1899-2018·2018-08-08

    Griffith Labs Recalls Romano Garlic Seasoning Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling 50-pound bags of Romano Garlic Seasoning due to potential Salmonella contamination from a recalled whey ingredient.

    Product
    Romano Garlic Seasoning 50 pound bag Item 1000015205
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·18V517000·2018-08-06

    Micro Bird Transit Bus Recall for Seat Belt Anchorage Defect

    Micro Bird is recalling 2015-2018 G5, MB II, and T-Series transit buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in crashes.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, T-SERIES TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V519000·2018-08-06

    Garden State Recalls 2015 Double Deck Buses for Emergency Exit Defect

    Garden State Bus Group is recalling 2015 Double Deck Buses because the roof emergency exit is incorrectly located, potentially delaying evacuation during an emergency.

    Product
    GARDEN STATE — GARDEN STATE DOUBLE DECK BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E079000·2018-08-06

    Hale Recalls Kubota Diesel Pumps Due to Wiring Defect

    Hale Products Inc is recalling Kubota Diesel Powered Portable Pumps because improper wiring may prevent warning lamps from illuminating, increasing the risk of injury if the engine fails.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V516000·2018-08-06

    Micro Bird Recalls 2015-2018 School Buses for Seat Belt Defect

    Micro Bird is recalling 2015-2018 G5, MB II, and T-Series school buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V518000·2018-08-06

    Newmar Recalls 2018-2019 Motorhomes Due to Door Latch Adjustment Issue

    Newmar is recalling 2018-2019 motorhomes because improperly adjusted door latch rods may allow the entry door to open during transit.

    Product
    NEWMAR — NEWMAR DUTCH STAR, VENTANA LE, VENTANA, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V515000·2018-08-03

    Mercedes-Benz Recalls E-Class and CLS Models for Air Bag Calibration Issue

    Mercedes-Benz is recalling 2018 E-Class and 2019 CLS vehicles because the front passenger air bag may not deactivate if a child seat is installed, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 400, AMG E63S, E 300, E43 AMG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E078000·2018-08-03

    Honda Recalls Africa Twin Centerstand Kits Due to Detachment Risk

    Honda is recalling Genuine Accessory Centerstand Kits for 2016-2018 Africa Twin motorcycles because a broken circlip can cause the stand to detach, creating a road hazard or causing the bike to fall.

    Product
    HONDA — HONDA CRF1000A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V512000·2018-08-03

    Mercedes-Benz Recalls 2018 GLE Models for Sunroof Adhesion Defect

    Mercedes-Benz is recalling 2018 GLE 350 and AMG GLE43 vehicles because the panoramic sunroof may not be properly adhered, creating a road hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, AMG GLE43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V507000·2018-08-02

    Thor Motor Coach Recalls Aria and Venetian Motorhomes for Brake Bolt Issue

    Thor Motor Coach is recalling 2017-2019 Aria and Venetian motorhomes because brake caliper mounting bolts may loosen, potentially reducing braking performance.

    Product
    THOR — THOR, THOR MOTOR COACH ARIA, VENETIAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V509000·2018-08-02

    GM Recalls 2018 Chevrolet Express and GMC Savana for TPMS Calibration

    General Motors is recalling 2018 Chevrolet Express and GMC Savana vans because the tire pressure monitoring system may be incorrectly calibrated, potentially delaying low-pressure warnings.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18200·2018-08-02

    Hill Topper Electric Bike Motor Controllers Recalled for Crash Hazards

    CPSC recalls Hill Topper electric bike motor controllers that may accelerate on their own, posing crash and injury risks to riders.

    Product
    Hill Topper Electric Bike motor controller circuit board
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2521-2018·2018-08-01

    DePuy CORAIL Femoral Stems Recalled Due to Incorrect Size Labeling

    DePuy Orthopaedics is recalling two lots of CORAIL femoral stems labeled as Size 11 but actually Size 12 due to fit and mechanical risks.

    Product
    CORAIL Cementless Femoral Stem HA Coated Standard Size 11, Catalog No. 3L92511
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-2498-2018·2018-08-01

    Philips Allura Xper Medical Imaging Systems Recalled for Shutter Reset Issue

    Philips Healthcare is recalling 459 Allura Xper systems because shutter positions reset when procedure types change, potentially affecting imaging accuracy.

    Product
    Allura Xper Product Usage: Vascular,cardiovascular and neurovascular imaging applications,including diagnostic, interventional and minimally invasive procedures. Cardiac imaging applications including diagnostics, interventional and minimally invasive procedures (such as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2525-2018·2018-08-01

    Siemens AXIOM Artis Angiography System Recalled for Defective Sealing

    Siemens is recalling six AXIOM Artis angiography systems in the US due to a defective sealing that could allow coolant to leak into electrical parts.

    Product
    AXIOM Artis with Laird Cooling Unit for SSFD: Material # 7555118. Artis is an angiography system developed for single and biplane diagnostic imaging and interventional procedures.
    Category
    Medical Device
    Distribution
    7 states
  • HighFDA (Devices)·Z-2517-2018·2018-08-01

    Implantcast Recalls Hip Implant Inserts Due to Retaining Ring Mounting Risk

    Implantcast GmbH is recalling specific 2M insert 15degree orthopedic hip implant components because the retaining ring may be incorrectly mounted.

    Product
    2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip implant acetabular component. Size 38/39 mm REF number 02423839 Size 42/44 mm REF number 02424244 Size 44/48 mm REF number 02424448 Size 46/52 mm REF number 02424652
    Category
    Medical Device
    Distribution
    3 states