State

Hawaii product recalls

73,584 recalls have nationwide distribution and so reach Hawaii. 2,772 additional recalls listed Hawaii specifically in their distribution scope.

What the numbers show

Total: 2,772
Critical: 331
Severe: 717
Most recent: 2026-10-14

Of the 2,772 recalls naming Hawaii we have scored against our rubric, 331 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 717 (26%) are Severe.

Which agencies issued them

These figures cover only the 2,772 recalls whose distribution notice names Hawaii specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26226–26250 of 76356

HighFDA (Devices)·Z-1273-2021·2021-03-24
Philips CT Systems Recalled for Potential Couch Movement Failure
Philips is recalling 109 CT systems because a defect in the Incisive CT couch actuators could cause the couch to fail to self-lock and move downward unexpectedly.
Product
Philips CT systems are advanced continuous-rotation computed tomography systems suitable for a wide range of computed tomographic (CT) applications - Product Usage: intended for use in the head and whole body.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1276-2021·2021-03-24
Epimed Feth-R-Kath Catheter Recalled for Coating Deterioration
Epimed International is recalling Feth-R-Kath Catheters because the outer coating may crack or flake off. The recall covers 5,835 units distributed nationwide.
Product
Feth-R-Kath Catheter, 19g x 24". Intended Use:Radlo Opaque Epidural Catheter Catalog #: 157-1924 Intended for epidural anesthesia and is limited to placement of 72 hours or less
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1253-2021·2021-03-24
Siemens SOMATOM CT Software Recall for Workflow Interruptions
Siemens is recalling specific software versions for SOMATOM CT systems due to sporadic errors that may interrupt scanning workflows and delay diagnosis.
Product
Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed tomography systems as follows: SOMATOM go.Now (Model 11061610)SOMATOM go.Up (Models 11061620 & 11061628) SOMATOM go.All (Model 11061630) SOMATOM go.Top (Models 11061640 & 11061648) SOMATOM go.Sim…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1254-2021·2021-03-24
Mindray BeneVision Distributed Monitoring System Recalled for Intermittent Freezes
Mindray is recalling 1,938 BeneVision Distributed Monitoring Systems because they may intermittently freeze, causing telemetry data to stop communicating to the central system.
Product
Mindray BeneVision Distributed Monitoring System( DMS) 1. p/n 115-051209-00 2. p/n 115-034414-00 and 115-034413-00 when used with the following software versions: 03.04.00 04.01.00 04.03.00 04.04.00 04.04.01
Category
Medical Device
Distribution
Distributed nationwide
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 (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