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.

26201–26225 of 50460

  • HighFDA (Devices)·Z-1043-2019·2019-04-03

    Smith & Nephew Recalls Journey II XR Tibial Posterior Keel Punch

    Smith & Nephew is recalling 65 units of the Journey II XR Tibial Posterior Keel Punch due to a higher than anticipated occurrence of bone fracture during use.

    Product
    JOURNEY II XR TIBIAL POSTERIOR KEEL PUNCH SZ 3-4 , REF 74013987 The JOURNEY II XR Tibial Posterior Keel Punch is a reusable surgical instrument used to prepare the proximal tibial to receive a JOURNEY II XR tibial baseplate.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1047-2019·2019-04-03

    Avitus Bone Harvester Recalled for Potential Sterility Compromise

    Avitus Orthopaedics is recalling 207 Bone Harvesters due to a breach in the sterile barrier pouch that may compromise device sterility.

    Product
    Avitus¿ Bone Harvester w/ Filter Insert - 5mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-210 The Avitus¿ Bone Harvester is intended to harvest cancellous bone and bone marrow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1046-2019·2019-04-03

    Avitus Bone Harvester Recalled for Potential Sterility Compromise

    Avitus Orthopaedics is recalling 508 Bone Harvester units because a breach in the sterile barrier pouch may compromise the device's sterility.

    Product
    Avitus¿ Bone Harvester w/ Filter Insert - 8mm intended to harvest cancellous bone and bone marrow Catalog Number: BH-110 The Avitus¿ Bone Harvester is intended to harvest cancellous bone and bone marrow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1056-2019·2019-04-03

    Philips URODiagnost Eleva X-ray System Recalled for Missing Locking Plate

    Philips North America, LLC is recalling URODiagnost Eleva X-ray systems because a missing locking plate may cause unexpected stand or table tilt movement that users cannot stop.

    Product
    URODiagnost Eleva, Product codes 708026, 708027, 708028 Product Usage: The Philips OmniDiagnost is a multi-functional, universal X-ray system with remote-controlled facilities. It performs a wide range of routine examinations and interventional procedures include…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1052-2019·2019-04-03

    Philips MultiDiagnost-Eleva Imaging System Recalled for Missing Locking Plate

    Philips is recalling MultiDiagnost-Eleva imaging systems because a missing locking plate may cause unexpected stand or table tilt movement that users cannot stop.

    Product
    MultiDiagnost-Eleva, Product codes 708032, 708036 Product Usage: As a multifunctional I universal imaging application system, General RIF, Fluoroscopy, Radiography and Angiography can be performed along with more specialized interventional applications on human patients.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1041-2019·2019-04-03

    Kendall SCD Express Sterile Sleeves Recalled for Sterility Failure

    COVIDIEN LLC is recalling Kendall SCD Express Sterile Sleeves (Thigh Length) because they were distributed without undergoing sterilization.

    Product
    Kendall SCD Express Sterile Sleeves (Thigh Length), Model Number 9736
    Category
    Medical Device
    Distribution
    3 states
  • HighCPSC·19096·2019-04-02

    Spector & Co. Recalls T119 Elf Power Bank Chargers Due to Fire Hazard

    Spector & Co. is recalling T119 Elf power bank chargers because they can overheat and pose a fire hazard. No injuries or property damage have been reported.

    Product
    T119 Elf power bank chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V268000·2019-04-02

    Spartan Metrostar Emergency Vehicles Recalled for Brake Light Wiring Defect

    Precision Industries is recalling 2017-2018 Spartan Metrostar emergency vehicles because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.

    Product
    SPARTAN — SPARTAN METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19732·2019-04-02

    John Deere Recalls Snow Blower and Broom Attachment Kits for Missing Manuals

    John Deere is recalling about 2,550 snow blower and broom attachment kits because they are missing the Operator's Manual, which poses an injury hazard.

    Product
    Attachment Kits for John Deere Snow Blowers and 52-inch Brooms
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V270000·2019-04-02

    Jayco Recalls Motorhomes Due to Missing Blower Motor Fuse

    Jayco is recalling 2014-2019 Precept, 2016-2019 Alante, and 2019 Precept Prestige motorhomes because a missing fuse in the blower motor circuit may cause wiring to overheat and increase fire risk.

    Product
    JAYCO — JAYCO ALANTE, PRECEPT, PRECEPT PRESTIGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V267000·2019-04-02

    KME Fire Apparatus Recall for Sliding Cover Lock Defect

    KME is recalling specific fire apparatus models because the gas spring lock for the sliding cover may fail to engage, creating an injury risk.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER, COMMERCIAL PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V261000·2019-04-01

    Eldorado Shuttle Bus Recall for Reversed Backup Camera Image

    Eldorado is recalling 2017-2018 shuttle buses because backup camera displays may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    ELDORADO — ELDORADO ADVANTAGE, AEROTECH, AERO ELITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V259000·2019-03-29

    Supreme Service Body Vehicles Recalled for Missing Head Impact Padding

    Supreme Corporation is recalling 2014-2018 Service Body vehicles on Ford Transit chassis because they may lack required padded trim for head impact protection.

    Product
    SUPREME — SUPREME SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V256000·2019-03-28

    Acura Recalls MDX Models Due to Tailgate Light Moisture Ingress

    Honda is recalling 2014-2019 Acura MDX and 2017-2019 MDX Sport Hybrid vehicles because moisture may enter the tailgate lid lights, causing them to fail and reducing vehicle visibility.

    Product
    ACURA — ACURA MDX SPORT HYBRID, MDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V251000·2019-03-28

    Fire Equipment Sales Recalls Two Emergency Vehicles With Faulty Brake Lights

    Fire Equipment Sales & Service is recalling two 2018 emergency vehicles because their brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    FORD — FORD, FREIGHTLINER F-550, M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19092·2019-03-28

    Midwest-CBK Recalls Baby Rattle Socks Due to Choking Hazard

    Midwest-CBK is recalling Baby Rattle Socks because small ornaments can detach, posing a choking hazard to young children. No injuries have been reported.

    Product
    Baby Rattle Socks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V250000·2019-03-28

    Road Rescue Ultramedic Recalled for Backup Camera Display Defect

    REV Ambulance Group is recalling 2018-2019 Road Rescue Ultramedic vehicles because backup camera displays may revert to factory settings, causing the image to reverse.

    Product
    ROAD RESCUE — ROAD RESCUE ULTRAMEDIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19094·2019-03-28

    Interline Brands Recalls ProPlus Brass Swivel Fittings Due to Fire Hazard

    Interline Brands is recalling ProPlus Brass Flare Swivel Fittings because they can leak, posing a fire hazard. Consumers should contact Interline for a full refund or replacement.

    Product
    ProPlus Brass Flare Swivel Fittings
    Category
    Consumer Product
    Distribution
    Distributed nationwide