The Recall Desk

State

Kentucky product recalls

73,597 recalls have nationwide distribution and so reach Kentucky. 7,203 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total
7,203
Critical
1,407
Severe
2,026
Most recent
2026-10-21

Of the 7,203 recalls naming Kentucky we have scored against our rubric, 1,407 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,026 (28%) are Severe.

Which agencies issued them

These figures cover only the 7,203 recalls whose distribution notice names Kentucky specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27801–27825 of 80800

  • HighFDA (Devices)·Z-1272-2021·2021-03-24

    Accuray CyberKnife Treatment Delivery System Recalled for Loose Set Screws

    Accuray is recalling 243 CyberKnife Treatment Delivery Systems because set screws can loosen, allowing the treatment couch to roll unexpectedly.

    Product
    CyberKnife Treatment Delivery System - Product Usage: indicated for image-guided stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V208000·2021-03-24

    2021 Genesis GV80 High-Pressure Fuel Tube Recall: Fire Risk

    Hyundai is recalling certain 2021 Genesis GV80 and G80 vehicles with 2.5-liter turbo engines due to a high-pressure fuel tube that may not seal properly, potentially allowing fuel to leak and increase fire risk.

    Product
    GENESIS — GENESIS GV80, G80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1267-2021·2021-03-24

    Ortho-Clinical VITROS SARS-CoV-2 Antigen Reagent Pack Recall for False Results

    Ortho-Clinical Diagnostics is recalling VITROS SARS-CoV-2 Antigen Reagent Packs used with Remel M4RT Viral Transport Media due to potential false reactive results.

    Product
    VITROS SARS-CoV-2 Antigen Reagent Pack - The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent Pack when used in combination with the VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Calibrator is a chemiluminescent immunoassay intended for the qualitative detection…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1270-2021·2021-03-24

    Canon Medical Recalls Catheterization Tables Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 INTERVENTIONAL ANGIOGRAPHY SYSTEMS because loose bolts may cause the table to tilt.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000C Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V207000·2021-03-24

    2021 Thomas Built Buses Saf-T-Liner C2 Recalled for Damaged Valve Stems

    Daimler Trucks North America is recalling 2021 Thomas Built Buses Saf-T-Liner C2 school buses because tire valve stem extensions may be damaged by brake calipers, risking tire pressure loss.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V199000·2021-03-24

    2021 BMW X3 and X4 Fuel Tank Weld May Separate, Increasing Fire Risk

    BMW is recalling certain 2021 X3 and X4 vehicles due to a fuel tank weld that may fail, allowing fuel to leak and increasing fire risk. All repairs have been completed.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1268-2021·2021-03-24

    Carestream Dental CS 3600 Tips Recalled for Detachment Risk

    Carestream Dental is recalling CS 3600 Single Use Normal Tips because the mirror may become detached and fall from the unit.

    Product
    Carestream Dental CS 3600 Single Use Normal Tips, Catalog Number 5941216 - Product Usage: used to record the topographic characteristics of teeth or dental impressions in three dimensions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1275-2021·2021-03-24

    Sirtex Medical Recalls SIROS D-Vial Prep Sets Due to Particulate Matter

    Sirtex Medical Limited is recalling SIROS D-Vial Prep Sets because of a potential presence of particulate matter in the D-Vial.

    Product
    SIROS D-Vial Prep Set, Product Code SIR-10200 - Product Usage: intended for single use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V209000·2021-03-24

    2021 Western Star 4700 and Freightliner Cascadia clutch assembly recall

    Daimler Trucks North America recalls certain 2021 Western Star 4700 and Freightliner Cascadia vehicles because the clutch flange may break, causing clutch disengagement and crash risk. Dealers will replace the clutch assembly free of charge.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4700, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1271-2021·2021-03-24

    Canon Catheterization Table Recall Due to Potential Tilt Hazard

    Canon Medical System is recalling 145 interventional angiography systems because the table may tilt if fastening bolts become loose.

    Product
    Canon INTERVENTIONAL ANGIOGRAPHY SYSTEM MODEL INFX-8000F Catheterization Table CAT-880B Canon CATHETERIZATION TABLE, MODEL CAT-880B INPUT 220V - Product Usage: indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1266-2021·2021-03-24

    Ortho-Clinical VITROS SARS-CoV-2 Antigen Reagent Recalled for False Results

    Ortho-Clinical Diagnostics is recalling VITROS SARS-CoV-2 Antigen Reagents because they may produce false reactive results when used with Remel M4RT Viral Transport Media.

    Product
    VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent- In Vitro Diagnostic. The VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Reagent Pack when used in combination with the VITROS Immunodiagnostic Products SARS-CoV-2 Antigen Calibrator is a chemiluminescent…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1251-2021·2021-03-24

    Cardinal Health Recalls McKesson Prevent M Needles Due to Safety Shield Defect

    Cardinal Health is recalling 108,000 McKesson Prevent M needles because the safety shield may fail to lock, posing a risk of needlestick injuries and exposure to bloodborne pathogens.

    Product
    McKesson PREVENT M NEEDLE (Magellan Technology) 25G X 5/8". A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 26558
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1250-2021·2021-03-24

    Cardinal Health Recalls Magellan Hypodermic Safety Needles Due to Locking Failure

    Cardinal Health is recalling Magellan Hypodermic Safety Needles because the safety shield may fail to lock, creating a risk of needlestick injuries and exposure to bloodborne pathogens.

    Product
    Magellan Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881850558
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21100·2021-03-24

    Flame King Recalls Hog 100-Pound Propane Cylinders Due to Fire Hazard

    Flame King is recalling Hog 100-pound propane cylinders because a manufacturing defect could cause gas leaks and fire. No injuries have been reported.

    Product
    Hog 100-pound Propane Cylinders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21101·2021-03-24

    Beal Birdie Belay Devices Recalled Due to Risk of Climber Injury

    Beal Sas is recalling about 1,400 Birdie Belay Devices because the hand lever can detach, preventing users from lowering climbers. No injuries have been reported.

    Product
    Beal Birdie Belay Devices
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E021000·2021-03-24

    Guangzhou Cougar LED Headlight Bulbs Recalled for Excessive Glare

    Guangzhou Cougar is recalling specific LED headlight bulbs that create excessive glare for oncoming drivers, increasing crash risk.

    Product
    EXTERIOR LIGHTING:HEADLIGHTS:BULBS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1252-2021·2021-03-24

    Cardinal Health Recalls Magellan Syringes Due to Safety Shield Defect

    Cardinal Health is recalling Magellan 3 mL syringes with hypodermic safety needles because the safety shield may fail to lock, posing a needlestick risk.

    Product
    Magellan 3 mL Syringe with Hypodermic Safety Needle, 25 G x 5/8" (0.508 mm x 1.6 cm). A single lumen needle intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. Product Code: 8881833558
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0304-2021·2021-03-24

    Spironolactone Tablets Recalled Due to Potential Labeling Mix-Up

    Bryant Ranch Prepack is recalling 12 bottles of Spironolactone 50 mg tablets because they may contain 25 mg tablets due to a labeling error.

    Product
    Spironolactone Tablets, USP, 50 mg, packaged in 30-count bottles, Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA, NDC 63629-1067-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1249-2021·2021-03-24

    Medline Recalls RNA Medical Hemoglobin Control Product Due to Shipment Compromise

    Medline Industries is recalling 4 units of RNA Medical Hemoglobin Control product because the product was compromised during shipment. The recall affects distribution in Kentucky, Pennsylvania, and Ohio.

    Product
    RNA MEDICAL, QCHGB HEMOGLOBIN CONTROL, MULTI, REF QC HGB - Product Usage: monitoring the performance of Hemocue Hemoglobin Analyzers. It provides a convenient method of performing periodic QC checks to verify correct system measurement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0363-2021·2021-03-24

    Electrolit Fruit Punch Recalled for Undeclared Red Dye

    Laboratorios Pisa is recalling Electrolit Fruit Punch bottles and 6-packs because they contain undeclared FD&C Red No. 40.

    Product
    Electrolit Ponche/Fruit Punch; in 625 mL/21 oz and 300ML/10oz bottles; and Electrolit Fruit Punch 6 Pack, 625mL/21 oz; Packaged in a polypropylene bottle with volume capacity 625 mL and a polypropylene lid and liner with a high-density polyethylene safety ring.
    Category
    Food
    Distribution
    22 states
  • ModerateFDA (Drugs)·D-0301-2021·2021-03-24

    Akorn Recalls Gabapentin Oral Solution Due to Impurity Specifications

    Akorn, Inc. is recalling Gabapentin Oral Solution because it failed impurity specifications during stability testing. The product was distributed nationwide.

    Product
    Gabapentin Oral Solution, 250 mg/5 mL, 5 mL per unit dose cup, four unit dose cups per tray, For Institutional Use Only, Rx only, Hi-Tech Pharmacal Co., Inc, Amityville, NY 11701, NDC Tray: 50383-311-07; NDC Unit Dose Cup 50383-311-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0308-2021·2021-03-24

    Breckenridge Recalls Omeprazole Capsules Due to Unknown Impurities

    Breckenridge Pharmaceutical is recalling 3,146 bottles of Omeprazole Delayed-Release Capsules, 20 mg, due to out-of-specification results for unknown impurities.

    Product
    Omeprazole Delayed-Release Capsules, USP, 20 mg, 1000 count bottles, Rx Only, distributed by Breckenridge Pharmaceutical, Inc., Berlin, CT, Manufactured by Tow Pharmaceutical Europe, S.L., Martorelles (Barcelona), Spain NDC 51991-643-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0306-2021·2021-03-24

    Edge Pharma Recalls Methacholine Challenge Test Kits Due to Storage Labeling Error

    Edge Pharma is recalling Methacholine Challenge 5-Syringe Test Kits because they were labeled with incorrect room temperature storage conditions instead of the required refrigerated conditions.

    Product
    Methacholine Challenge 5-Syringe Test Kits, Sterile Inhalation Solution, Preservative Free, 3 mL per syringe, Edge Pharma, LLC, 856 Hercules Dr., Dolchester, VT 06448 NDC # 05446-1600-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0364-2021·2021-03-24

    Electrolit Fruit Punch Zero Recalled for Undeclared Red Dye

    Laboratorios Pisa Sa De Cv is recalling 571,590 bottles of Electrolit Fruit Punch Zero because the product contains undeclared FD&C Red No. 40.

    Product
    Electrolit Fruit Punch Zero, 625ML/21OZ packaged in a polypropylene bottle with volume capacity of 625mL and with a polypropylene lid and liner with a high-density polyethylene safety ring.
    Category
    Food
    Distribution
    22 states
  • LowFDA (Drugs)·D-0309-2021·2021-03-24

    Teva Recalls Romidepsin Injection Vials Due to Impurity Failures

    Teva Pharmaceuticals is recalling 1,416 vials of Romidepsin Injection because stability testing revealed out-of-specification impurities.

    Product
    Romidepsin Injecton, 27.5 mg/5.5 mL (5 mg/mL) Rx Only, 5.5 ml vial, Teva Pharmaceuticals USA, Inc. NDC 0703-4004-01
    Category
    Drug
    Distribution
    Distributed nationwide