State

Hawaii product recalls

72,820 recalls have nationwide distribution and so reach Hawaii. 2,765 additional recalls listed Hawaii specifically in their distribution scope.

What the numbers show

Total: 2,765
Critical: 333
Severe: 566
Most recent: 2026-09-02

Of the 2,765 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 566 (20%) are Severe.

Which agencies issued them

These figures cover only the 2,765 recalls whose distribution notice names Hawaii specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

726–750 of 75585

HighCPSC·26611·2026-07-09
Kobalt 24V and 48V Yard Power Tools with USB-C Batteries Recalled for Fire Risk
Greenworks Tools recalls Kobalt yard power tools with USB-C batteries due to risk of fire when batteries are charged via the USB-C port while inserted in the tool. The firm received 34 reports of batteries smoking, sparking, or catching fire, with no injuries reported.
Product
Kobalt 24V and 48V Trimmers, Blowers, Mowers, Chainsaws and Pruning Saws with USB-C Batteries
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26609·2026-07-09
WonderStone Infant Walkers Recalled for Fall Hazard Risk
WonderStone Infant Walkers sold on Walmart.com violate mandatory infant-walker standards because they can fit through doorways and fail to stop at steps, posing a risk of serious injury or death from falls. No injuries have been reported.
Product
WonderStone Infant Walkers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26605·2026-07-09
Cuisinart Propel Four Burner Gas Grill Recalled Due to Laceration Hazard
Conair is recalling the Cuisinart Propel+ Four Burner 3-in-1 Gas Grill because the tempered glass window in the pizza oven can shatter during use, posing a laceration risk. About 12,660 units were sold.
Product
Cuisinart Propel+ Four Burner 3-in-1 Gas Grill with pizza oven
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26607·2026-07-09
Biometric Firearm Safes Recalled Due to Unauthorized-Access Hazard
BBRKIN and MouTec biometric firearm safes can be opened by unauthorized users, creating a serious injury and death risk. Consumers should immediately stop using the biometric feature and use the key only.
Product
BBRKIN and MouTec Biometric Firearm Safes
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26606·2026-07-09
Insignia Front Control Gas Ranges Recalled for Fire Hazard Risk
Best Buy is recalling about 3,820 Insignia Front Control Gas Ranges because the front-mounted knobs can be accidentally activated by humans or pets, creating a fire hazard risk.
Product
Insignia Front Control Gas Ranges
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2604-2026·2026-07-08
Omnipod DASH Pod insulin pump affected by external cannula damage
Insulet Corporation is recalling Omnipod DASH Pods worldwide due to external soft cannula damage during manufacturing that can cause insulin to leak around the pod instead of being delivered. This may lead to high blood glucose levels and, in severe cases, diabetic ketoacidosis or death.
Product
Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 (5-Pack), POD-BLE-I1-520 (Single Pod). 2. POD-BLE-I1-529 (10-Pack), POD-BLE-I1-520 (Single Pod). 3. BLE-I1-529 (10-Pack), BLE-I1-520 (Single Pod). 4. BLE-C1-529 (10-Pack), BLE-C1-520 (Single
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0652-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled for Lack of Sterile Assurance
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators because unsterilized units intended for further processing were distributed to customers outside the intended distribution channel, creating a lack of assurance of sterility.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2615-2026·2026-07-08
Reprocessed Electrophysiology Catheters Recalled for Residual Particles
Medline Industries is recalling reprocessed electrophysiology and ultrasound catheters with residual particles that may cause inflammation, infection, or blood clots if contacted with blood or the heart.
Product
Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 4 Elec. 10mm; Item no. 401305RH, St. Jude Medical Response" Diagnostic Electrophysiology Catheter 10 Elec. 2-5-2mm.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0647-2026·2026-07-08
ChloraPrep One-Step Antiseptic Applicators Distributed Without Sterilization
CareFusion 213, LLC is recalling 7,650 units of ChloraPrep One-Step antiseptic applicators distributed nationwide because unsterilized product intended for further processing was distributed through incorrect channels.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0650-2026·2026-07-08
ChloraPrep One-Step Sterile Solution Lacks Assurance of Sterility
CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) applicators distributed nationwide. The products were unsterilized and distributed outside the intended channel intended for further processing and sterilization.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2634-2026·2026-07-08
Boston Scientific CRE Wireguided Medical Device Recall Sterile Breach
Boston Scientific is recalling CRE Wireguided 10-12mm 240cm medical devices due to a potential sterile breach in the product packaging. The breach could compromise device sterility and affect patient safety.
Product
CRE Wireguided 10-12mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-1137-2026·2026-07-08
NARA ORGANICS Whole Milk Organic Infant Formula Recalled for Botulinum Contamination
NARA ORGANICS Whole Milk Organic Infant Formula in 24.7 oz and 14.1 oz sizes is being recalled nationwide because the product may be contaminated with Clostridium botulinum.
Product
a.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 24.7 OZ (700 G); UPC: 860013251901 b.) nara organics brand; Whole Milk Organic Infant Formula; Milk-based Powder with Iron; 0-12 months; NET WT 14.1 OZ (400 G); UPC: 8600
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2605-2026·2026-07-08
Omnipod Eros Pod Insulin Delivery Failure Risk
Insulet Corporation is recalling Omnipod (Eros) Pod units due to external soft cannula damage during manufacturing that can cause insulin leakage instead of delivery to the user. High blood glucose levels and serious complications including diabetic ketoacidosis (DKA) or death may result from under-delivery of insulin.
Product
Omnipod (Eros) Pod. Includes the below Model/REF Numbers: 1. POD-ZXP425 (10 Pack), POD- ZXP420 (Single Pod). 2. ZXR425 (10-Pack), ZXR420 (Single Pod). 3. ZXP425 (10 Pack), ZXP420 (Single Pod).
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0692-2026·2026-07-08
Revitaderm Wound Care Gel recalled for microbial contamination
Revitaderm Wound Care Gel has been recalled due to microbial contamination with Lysinibacillus fusiformis and other Bacillus species. The product was distributed nationwide and consumers should stop using it.
Product
Revitaderm Wound Care Gel, Benzalkonium Chloride 0.1%, packaged in 1.0 FL OZ (37 mL) bottle, shorter twist cap, Manufactured By: Blaine Labs, Inc. 11037 Lockport Place Santa Fe Springs, CA 90670, NDC 63347-120-02.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2610-2026·2026-07-08
Medline Convenience Kits with Recalled Swan-Ganz Catheters
Medline Convenience kits containing Swan-Ganz catheters are being recalled due to leaks and breakage of the proximal injectate lumen hub, which may lead to infection, medication loss, and blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA - ROOM SET UP DYNJ905503D DYNJ905503F DYNJ905503G
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2548-2026·2026-07-08
Hillrom VOLARA System P.CIRCUIT KIT Medical Device Recall for Oxygen Drop Risk
Baxter Healthcare is recalling the Hillrom VOLARA System P.CIRCUIT KIT (Model REF M08085) due to reports of air and medication leakage from the nebulizer cup, which can cause oxygen level drops and reduce treatment effectiveness.
Product
Hillrom VOLARA System P.CIRCUIT KIT (Single Patient Use Circuit), Model/Catalog Number REF M08085; Oscillation Lung Expansion Therapy, positive pressure breathing device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2624-2026·2026-07-08
Medtronic Harmony Delivery Catheter System Distal Tip Detachment Risk
Medtronic is recalling certain lots of the Harmony Delivery Catheter System due to a manufacturing issue that may cause the distal tip to detach from the delivery system during procedures.
Product
Medtronic Harmony Delivery Catheter System
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0658-2026·2026-07-08
Accucaine Lidocaine Injection Recalled for Lack of Sterility Assurance
Asclemed USA Inc. is recalling specific lots of Accucaine (Lidocaine HCl Injection USP, 1%) distributed nationwide due to lack of assurance of sterility. The affected product is distributed by Enovachem Pharmaceuticals.
Product
ACCUCAINE — ACCUCAINE (LIDOCAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0659-2026·2026-07-08
Lidocaine Hydrochloride Injection Recalled for Sterility Assurance
Asclemed USA Inc. is recalling Lidocaine Hydrochloride Injection USP, 1% (10 mg/mL) in 5 mL single dose ampules nationwide due to lack of assurance of sterility. The affected lots have expiration dates of 11/30/2026 and 04/30/2028.
Product
LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE ANHYDROUS)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2551-2026·2026-07-08
Hillrom VOLARA System patient circuits recalled for nebulizer cup leakage
Baxter Healthcare is recalling Hillrom VOLARA System patient circuits due to reports of air and medication leakage from the nebulizer cup, which can cause oxygen level drops and ineffective medication delivery.
Product
Hillrom VOLARA System P.CIRCUIT 5KIT AC, (Single Patient Use Circuit), Model/Catalog Number REF M08474; Oscillation Lung Expansion Therapy, positive pressure breathing device
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0651-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled Due to Sterility Assurance Loss
CareFusion 213, LLC is recalling ChloraPrep One-Step chlorhexidine gluconate and isopropyl alcohol applicators distributed nationwide because unsterilized units intended for further processing were distributed through the wrong channels.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0675-2026·2026-07-08
Cinacalcet Tablets Recalled for cGMP Deviations
Cipla USA, Inc. is recalling Cinacalcet Hydrochloride Tablets, 60 mg due to cGMP deviations involving the presence of N-nitroso-cinacalcet above acceptable daily intake levels.
Product
CINACALCET — CINACALCET (CINACALCET)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2463-2026·2026-07-08
Ventilator breathing circuit sets may obstruct exhalation valve
Hamilton Medical AG is recalling coaxial breathing circuit sets used with three ventilator models because membranes may stick to the expiratory valve body, preventing proper gas exhalation and potentially causing inadequate ventilation.
Product
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2620-2026·2026-07-08
Thyroid FNA Pack-RX Surgical Kit Recalled for Bacterial Contamination
Windstone Medical Packaging is recalling AMS Thyroid FNA Pack-RX surgical kits due to contamination with Paenibacillus phoenicis bacteria found in included Webcol alcohol prep pads.
Product
A M S, ALIGNED MEDICAL SOLUTIONS, Thyroid FNA Pack-RX, Pack Number AMS17729, surgical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0648-2026·2026-07-08
ChloraPrep One-Step Antiseptic Applicators recalled for lack of sterility assurance
CareFusion is recalling ChloraPrep One-Step antiseptic applicators because unsterilized units intended for further processing were distributed outside the intended channel, creating a sterility assurance gap.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide