State

Hawaii product recalls

73,509 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: 333
Severe: 715
Most recent: 2026-10-14

Of the 2,772 recalls naming Hawaii we have scored against our rubric, 333 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 715 (26%) are Severe.

Which agencies issued them

These figures cover only the 2,772 recalls whose distribution notice names Hawaii specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23301–23325 of 76281

HighFDA (Devices)·Z-0278-2022·2021-12-01
Imaging device ceiling mount assembly may detach, posing injury risk
A ceiling-mounted component on Philips CT imaging equipment may detach due to wear. This poses a risk of injury to patients, operators, or staff in operating rooms.
Product
Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini GXL 16 Slice System Number: 882410 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0306-2022·2021-12-01
BD Nexiva IV Catheters Recalled Due to Non-Sterile Packaging Breach
Becton Dickinson is recalling BD Nexiva IV catheter systems because of a packaging breach that renders them non-sterile. The recall affects 155,840 devices distributed nationwide.
Product
BD Nexiva, 20 GA 1.00 IN (1.1 X 25 mm), 3660 ml/hr. 61ml/min; Closed IV Catheter System- Dual port -61 mL/min (3660 mL/hr)-0.5mL, REF 383536; BD Q-Style Luer Access Split Septum BD Vialon Material; BD Instaflash Needle Technology; Rx Only, Sterile EO. BD Nexiva closed IV…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0277-2022·2021-12-01
CT imaging system ceiling mount bracket shaft wear may cause equipment to fall
A CT fluoroscopy imaging system ceiling mount's bracket shaft may wear excessively and go undetected, potentially causing the bracket to detach and fall, risking injury to patients, operators, or service personnel.
Product
Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - CT Vision ACQSIM CT System Number: 728209 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0280-2022·2021-12-01
Philips CT Fluoroscopy Ceiling Mount Bracket Wear and Detachment Hazard
Philips Continuous CT Fluoroscopy ceiling mounts may experience monitor bracket assembly wear that goes undetected, potentially causing the bracket to detach and fall on patients, operators, or bystanders during surgery.
Product
Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini TF 16 System Number: 882470 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21C005000·2021-12-01
Clek Recalls Foonf and Fllo Convertible Child Seats for Foam Choking Hazard
Clek is recalling specific Foonf and Fllo convertible child seats because loose foam pieces can pose a choking hazard to children.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0238-2022·2021-12-01
Philips Azurion System Recall for 3D Image Reconstruction Defect
Philips Healthcare is recalling Azurion systems with software releases 2.1(L1) and 2.1(L2) due to a software defect that prevents proper reconstruction of 3D X-ray images when the detector is positioned outside required tolerance.
Product
Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0272-2022·2021-12-01
Clinical Chemistry Analyzer Software Defects May Produce Inaccurate Results
Abbott ARCHITECT clinical chemistry analyzers with software 9.41 and earlier contain defects affecting calibration, sample handling, and quality control that may produce inaccurate diagnostic results.
Product
ARCHITECT c4000 REF 02P24-01/2P24, 1P86, 1R24, and 1R25; ARCHITECT c8000 REF 01G06-11/1G06; ARCHITECT c16000 REF 03L77-01/3L77;
Category
Medical Device
Distribution
50 states
HighFDA (Devices)·Z-0301-2022·2021-12-01
Siemens Artis Q angiography systems may fail to deliver x-ray during procedures
Siemens Artis Q angiography systems may fail to release x-ray when source-to-image distance lift and x-ray release are activated simultaneously, causing procedure delays.
Product
Artis Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848281
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V935000·2021-12-01
Audi Recalls 2022 E-Tron GT Vehicles Due to Air Suspension Defect
Volkswagen Group of America is recalling 2022 Audi E-Tron GT vehicles because a loose retaining ring on air suspension struts may compromise handling and increase crash risk.
Product
AUDI — AUDI E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0295-2022·2021-12-01
Medtronic Wireless Recharger Model WR9200 Becomes Unresponsive on Improper Use
Medtronic is recalling the Wireless Recharger Model WR9200 used with RestoreUltra and RestoreSensor neurostimulator implants. The recharger becomes unresponsive if charging instructions from the user guide are not followed correctly.
Product
Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger Kit used by the RestoreUltra (Model 37712), RestoreSensor (Model 37714), Restore Ultra SureScan MRI (Model 97712), and RestoreSensor SureScan MRI (Model 97714) implantable neurostimulators.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0283-2022·2021-12-01
CT Scanner Software Issue May Interrupt Diagnostic Workflows and Delay Diagnoses
Siemens SOMATOM Force CT scanners with software syngo.CT VB20 may experience workflow interruptions, causing diagnosis delays and requiring additional patient scans and contrast media. No illnesses or injuries have been reported.
Product
SOMATOM Force with software syngo.CT VB20 Model #10742326
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0284-2022·2021-12-01
CT Scanner Software Issue Causes Workflow Interruptions and Diagnostic Delays
A software issue in SOMATOM Definition AS CT scanners may cause workflow interruptions, leading to diagnostic delays and the need for patient rescans. The recall affects approximately 665 units distributed nationwide.
Product
SOMATOM Definition AS with software syngo.CT VB20 Model #8098027
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0240-2022·2021-12-01
Medical X-Ray Systems Missing Required Radiation Warning Labels
Philips Healthcare is recalling ProxiDiagnost N90 diagnostic X-ray systems that lack required FDA radiation warning labels. Some units nationwide were found missing the mandatory radiation safety labels and certification statements required by federal standards.
Product
ProxiDiagnost N90 is multi-functional general R/F systems.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0303-2022·2021-12-01
Siemens Artis Q.zen Angiography System May Fail to Fire X-rays During Simultaneous Operations
Three Siemens Artis Q.zen angiography systems may fail to fire X-rays when the source-to-image distance lift is activated simultaneously with X-ray commands. This causes a procedural delay.
Product
Artis Q.zen floor with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848353
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0298-2022·2021-12-01
Siemens Artis Zee Angiography System Software May Prevent X-Ray Activation
Siemens is recalling 19 units of its Artis zee angiography system due to a software issue that may prevent x-ray activation under specific operating conditions, causing procedural delay.
Product
Artis zee multi-purpose with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10094139
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0297-2022·2021-12-01
Siemens Artis zee x-ray system may delay imaging delivery during procedures
Siemens is recalling Artis zee ceiling-mounted x-ray imaging systems equipped with VD12 software. A software issue may prevent x-ray delivery when the source-to-image distance lift is activated during procedures, resulting in procedural delays.
Product
Artis zee ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number:10094137
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0275-2022·2021-12-01
da Vinci Surgical Drapes Recalled for Incorrect Expiration Date on Packaging
Intuitive Surgical recalls 1,740 da Vinci Instrument Arm Drapes due to incorrect expiration dates on package labeling. The error may prevent accurate verification of sterility assurance dates.
Product
The da Vinci Xi and X surgical systems (IS4000 and IS4200) each consist of three main components: the Surgeon Console (SC), the Vision Cart (VC), and the Patient Cart (PC). The Patient Cart is the operative component of the system and its primary function is to support the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0258-2022·2021-12-01
Diclofenac Sodium Topical Solution recalled for defective container
Teligent Pharma, Inc. is recalling Diclofenac Sodium Topical Solution USP 1.5% w/w due to a defective container. The recall affects approximately 2,664 bottles distributed nationwide.
Product
Diclofenac Sodium Topical Solution USP, 1.5 w/w, 5 fl oz (150 mL) plastic bottles, Rx only, Teligent Pharma, Inc., Buena, New Jersey, 08310, NDC 52565-002-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0259-2022·2021-12-01
Diclofenac Sodium Topical Solution recalled for defective container
Teligent Pharma, Inc. is recalling Diclofenac Sodium Topical Solution USP 1.5% due to a defective container. The recall affects 5,400 units distributed nationwide.
Product
Diclofenac Sodium Topical Solution USP, 1.5 w/w, 5 fl oz (150 mL) plastic bottles, Rx only, Teligent Pharma, Inc., Buena, New Jersey, 08310, NDC 70512-025-05.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0296-2022·2021-12-01
Medical Imaging System May Fail to Release X-rays Under Specific Conditions
Siemens Artis zee floor angiography systems may fail to release x-rays when the SID lift and x-ray functions are activated simultaneously, causing procedural delay. Three units are affected.
Product
Artis zee floor with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10094135
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0305-2022·2021-12-01
Siemens Artis Q.zen Angiography System X-Ray Imaging Delay Issue
Siemens has recalled two Artis Q.zen angiography systems due to a software issue that may prevent x-ray imaging and delay procedures when SID lift and x-ray controls are activated simultaneously.
Product
Artis Q.zen biplane with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number:10848355
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0299-2022·2021-12-01
Siemens Artis Zee Biplane X-ray Imaging System Software Malfunction
Siemens Artis zee biplane X-ray imaging systems may fail to release X-rays when the source-to-image distance lift is activated simultaneously, resulting in procedural delays.
Product
Artis zee biplane with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10094141
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0302-2022·2021-12-01
Siemens Artis Q Biplane X-ray System Software Imaging Delay Issue
Siemens Medical Solutions is recalling 15 Artis Q biplane diagnostic x-ray systems due to a software issue in the VD12-angiography subsystem. When source-to-image distance lift is activated simultaneously with x-ray release, the system fails to activate and displays an error message, causing procedural delay.
Product
Artis Q biplane with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848282
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0300-2022·2021-12-01
Siemens Artis Q floor angiography system: X-ray failure during SID lift operation
Siemens Artis Q floor angiography systems may fail to produce x-ray when SID lift movement is activated during x-ray release, resulting in procedural delays. The system displays an error message.
Product
Artis Q floor with software VD12- angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848280
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0304-2022·2021-12-01
Siemens Artis Q.zen Angiography System X-ray Activation Failure
Siemens is recalling 15 Artis Q.zen angiography systems that may fail to generate x-rays when the lift mechanism and x-ray release are activated simultaneously, potentially causing a procedural delay.
Product
Artis Q.zen ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848354
Category
Medical Device
Distribution
Distributed nationwide