State

Nevada product recalls

72,820 recalls have nationwide distribution and so reach Nevada. 5,692 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total: 5,692
Critical: 951
Severe: 1,476
Most recent: 2026-09-02

Of the 5,692 recalls naming Nevada we have scored against our rubric, 951 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,476 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,692 recalls whose distribution notice names Nevada specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

751–775 of 78512

SevereFDA (Devices)·Z-2640-2026·2026-07-08
Cyberknife Treatment Delivery System Collimator Docking Failure Risk
Accuray Incorporated is recalling Cyberknife Treatment Delivery Systems equipped with the Xchange Robotic Collimator Changer due to a risk that the collimator may not fully dock and could fall from the housing if the in-room control pendant is used.
Product
Cyberknife Treatment Deliver System equipped with the Xchange Robotic Collimator Changer; Linear Accelerator
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V437000·2026-07-08
2026 Toyota Grand Highlander Hybrid rear axle carrier structural defect
Toyota is recalling certain 2026 Grand Highlander Hybrid and related models because the rear axle carriers may have insufficient material strength and could break, causing loss of vehicle control and increasing crash risk.
Product
TOYOTA — TOYOTA, LEXUS GRAND HIGHLANDER, GRAND HIGHLANDER HYBRID, TX, TX HYBRID
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2672-2026·2026-07-08
GORE TAG Thoracic Branch Endoprosthesis Side Branch Component Recall
W. L. Gore & Associates is recalling 467 GORE TAG Thoracic Branch Endoprosthesis Side Branch Components worldwide due to risk of catheter separation during deployment.
Product
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes Puerto Rico) and Canada: TSB080806A, TSB081006A, TSB081206A, TSB081506A, TSB081706A, TSB121506A, TSB121706A, TSB122006A EMEA Countries, Australia, New Zealand:
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0646-2026·2026-07-08
ChloraPrep One-Step Applicators Recalled for Lack of Sterility 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 sterility assurance.
Product
CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2621-2026·2026-07-08
Preop Kit-NS surgical kits recalled for bacterial contamination
A M S Preop Kit-NS surgical convenience kits are being recalled due to contamination with Paenibacillus phoenicis bacteria discovered during sterilization testing. The kits were distributed nationwide in PA, GA, CA, and WA.
Product
A M S, ALIGNED MEDICAL SOLUTIONS, Preop Kit-NS, Pack Number AMS18227, surgical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2603-2026·2026-07-08
Omnipod 5 Insulin Infusion Pods Recalled for External Cannula Damage
Insulet Corporation is recalling approximately 4.9 million Omnipod 5 insulin pods due to external soft cannula damage during manufacturing that can cause insulin leakage and under-delivery, potentially leading to high blood glucose and serious diabetic complications.
Product
Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2. POD-OMNI-I1-6220. 3. OMNI-I1-6729 (10-Pack), OMNI-I1-6720 (Single Pod). 4. OMNI-I1-6220. 5. OMNI-I1-6720. 6. BLE-H1-529 (10-Pack), BLE-H1-520 (Single Pod).
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V438000·2026-07-08
BMW and Toyota vehicles recalled due to engine starter fire risk
BMW of North America, LLC is recalling various BMW and Toyota Supra models because the engine starter may overheat and catch fire.
Product
TOYOTA — TOYOTA, BMW SUPRA, Z4, X4, X3
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2619-2026·2026-07-08
DSAEK Pack-RX surgical kits recalled for bacterial contamination
Windstone Medical Packaging is recalling 1,080 DSAEK Pack-RX surgical convenience kits containing Webcol Large Alcohol Prep Pads contaminated with Paenibacillus phoenicis bacteria discovered during a sterilization audit.
Product
A M S, ALIGNED MEDICAL SOLUTIONS, DSAEK Pack-RX, Pack Number AMS12394B, surgical convenience kit
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2550-2026·2026-07-08
Hillrom VOLARA System patient circuits recalled for nebulizer leakage risk
Baxter Healthcare is recalling Hillrom VOLARA System patient circuits due to reports of air and medication leakage from the nebulizer cup, which can reduce oxygen levels and prevent proper medication delivery.
Product
Hillrom VOLARA System P.CIRCUIT KIT AC (Single Patient Use Circuit), Model/Catalog Number REF M08473; Oscillation Lung Expansion Therapy, positive pressure breathing device
Category
Medical Device
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 (Devices)·Z-2549-2026·2026-07-08
Hillrom VOLARA P.CIRCUIT Medical Device Nebulizer Cup Leakage Recall
Baxter Healthcare Corporation is recalling the Hillrom VOLARA P.CIRCUIT 5KIT medical device due to reports of air and medication leakage from the nebulizer cup, which can reduce oxygen levels and compromise medication delivery.
Product
Hillrom VOLARA P.CIRCUIT 5KIT (System Single Patient Use Circuit), Model/Catalog Number REF M08270; Oscillation Lung Expansion Therapy, positive pressure breathing device
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·26V441000·2026-07-08
BMW Recalls 29,119 Vehicles Due to Starter Relay Fire Risk
BMW is recalling 29,119 vehicles because a corroded starter relay may overheat and short circuit, increasing the risk of a fire.
Product
BMW — BMW 530E XDRIVE IPERFORMANCE, 740LE XDRIVE IPERFORMANCE, 530E IPERFORMANCE, 330E IPERFORMANCE
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2632-2026·2026-07-08
CRE Wireguided 6-8mm 240cm Medical Device Recall Worldwide
Boston Scientific Corporation is recalling the CRE Wireguided 6-8mm 240cm device worldwide due to a potential sterile breach of the packaging pouches.
Product
CRE Wireguided 6-8mm 240cm
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2607-2026·2026-07-08
Medline Convenience Kits with Swan-Ganz Catheters Recalled for Defects
Medline is recalling convenience kits containing Swan-Ganz catheters due to failures of the proximal injectate lumen hub that can cause leaks, lumen damage, and breakage, potentially resulting in infection, medication loss, or blood loss.
Product
Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR DYNJ901328G HEART A DYNJ903465K OPEN HEART DYNJ909090G SILVER CROSS OPEN HEART DYNJ906102M VPH OPEN HEART DYNJ902664M DYNJ902664N
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0653-2026·2026-07-08
IMULDOSA injection recalled due to lack of sterility assurance
Accord BioPharma is recalling IMULDOSA (ustekinumab-srlf) Injection due to lack of assurance of sterility. The affected lot was distributed nationwide.
Product
IMULDOSA — IMULDOSA (USTEKINUMAB-SRLF)
Category
Drug
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-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 (Food)·H-1128-2026·2026-07-08
MOGO PURE MORINGA OLEIFERA CAPSULES HERBAL SUPPLEMENT CONTAMINATION RECALL
MOGO PURE MORINGA OLEIFERA CAPSULES herbal supplement is recalled due to potential Salmonella Typhimurium contamination. The affected product was sold nationwide via online retailers.
Product
MOGO PURE MORINGA OLEIFERA CAPSULES, HERBAL SUPPLEMENT, 180 QUICK RELEASE VEGGIE CAPSULE, 100% PURE, 350 MG PER CAPSULE, SUPPLEMENT FACTS MORINGA POWDER 1050 mg, Ingredients: 100% Pure Moringa Leaf Powder (Moringa Oleifera), MANUFACTURED IN USA AND Marketed by: MOGO MIRINGA LLC,
Category
Food
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-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-2622-2026·2026-07-08
Surgical Convenience Kit Recalled for Bacterial Contaminant in Alcohol Prep Pads
Windstone Medical Packaging is recalling AMS Dr. Lewin Pack surgical convenience kits (45 units) distributed nationwide because they contain Webcol alcohol prep pads contaminated with Paenibacillus phoenicis bacteria.
Product
A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit
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-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-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 (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