State

Nevada product recalls

72,992 recalls have nationwide distribution and so reach Nevada. 5,693 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total: 5,693
Critical: 951
Severe: 1,477
Most recent: 2026-09-25

Of the 5,693 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 1,477 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,693 recalls whose distribution notice names Nevada specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8401–8425 of 78685

HighFDA (Drugs)·D-0202-2025·2025-01-22
FDA recalls glipiZIDE Extended-Release Tablets for failed dissolution specifications
Amerisource Health Services LLC is recalling glipiZIDE Extended-Release Tablets, 2.5 mg, due to failed dissolution specifications. Patients should contact their pharmacist or healthcare provider.
Product
glipiZIDE, Extended-Release Tablets, 2.5 mg, 30-count (3x10 blister cards) carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217, Carton NDC: 60687-480-21, Unit Dose NDC: 60687-480-11
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0835-2025·2025-01-22
Alcon Monarch III D Delivery Cartridge Recalled for Molding Defect Risk
Alcon is recalling 41,718 units of its Monarch III D Delivery Cartridge due to a molding defect that could scratch the intraocular lens during cataract surgery.
Product
Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description: Monarch¿ III D delivery cartridge Lens Guide, Intraocular Component: N/A
Category
Medical Device
Distribution
51 states
HighFDA (Devices)·Z-0959-2025·2025-01-22
Change Healthcare Cardiology Software Defect May Cause Incorrect Medication Administration
A software defect in Change Healthcare's Cardiology Hemodynamics software may cause clinicians to administer incorrect medications. The defect affects an autosave mechanism and has been distributed nationwide and internationally.
Product
Change Healthcare Cardiology Hemodynamics software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0881-2025·2025-01-22
Intuitive Surgical Bipolar Dissector Recalled for Frayed Grip Cables
Intuitive Surgical is recalling 8MM curved bipolar dissectors due to frayed or broken grip cables that could affect surgical instrument performance. Approximately 3,869 units were distributed nationwide and internationally.
Product
8MM,CURVED BIPOLAR DISSECTOR,IS4000 REF 471344
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0876-2025·2025-01-22
8MM Maryland Bipolar Forceps Recalled for Frayed Grip Cable
Intuitive Surgical is recalling 68,458 units of its 8MM Maryland Bipolar Forceps due to increased complaints about frayed or broken grip cables on the reusable surgical instruments.
Product
8MM,MARYLAND BIPOLAR FORCEPS,IS4000 REF 471172
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0938-2025·2025-01-22
Surgical Suction Tubes Recalled for Sterile Packaging Defects
ECONO STERILE suction tubes and surgical instruments (150 units, nationwide) are recalled for packaging defects that may breach the sterile barrier and create infection risk during medical procedures.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE YANKAUER SUCTION TUBE 8.5" C10, Model Number 96-4176; 2) ECONO STERILE YANKAUER SUCTION TUBE 11" CS10, Model Number 96-4177; 3) ECONO STERILE FRAZIER TUBE 6FR STERILE CS/25, Model Number 96-5434; 4) ECONO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0936-2025·2025-01-22
ECONO STERILE Medical Procedure Kits Recalled for Sterile Barrier Compromise
Sklar Instruments recalls ECONO STERILE medical procedure kits (300 units nationwide) due to packaging issues that may compromise sterile barrier integrity.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE BACKHAUS TWL CLP STER 3.5 CS50, Model Number 96-2630; 2) ECONO STERILE BACKHAUS TWL CLP STER 5.25 25, Model Number 96-2636; general purpose clips
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0935-2025·2025-01-22
Sklar Instruments Recalls Sterile Vein Hooks Due to Packaging Issues
Sklar Instruments is recalling 1,050 units of ECONO STERILE Vein Hooks due to packaging issues that may breach the sterile barrier. Products were distributed nationwide.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE VEIN HOOK 1.5MM STERILE CS/25, Model Number 96-4020M; 2) ECONO STERILE VEIN HOOK 2MM STERILE CS/25, Model Number 96-4021M; 3) ECONO STERILE VEIN HOOK 2.5MM STERILE CS/25, Model Number 96-4022M; venous proced
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0912-2025·2025-01-22
Cardinal Health Laryngoscopy Presource Kits Recalled for Endotoxin Contamination
Cardinal Health is recalling 512,786 Laryngoscopy Presource Kits due to potential endotoxin contamination in non-sterile surgical strips and patties. The kits were distributed to the United States, Canada, and Saudi Arabia.
Product
Cardinal Health Presource Kits: 1 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH2 ; 2 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH3 ; 3 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH4 ; 4 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH5 ; 5 ) STERILE LARYNGOSCOPY PACK, Cata
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0939-2025·2025-01-22
Sklar Instruments Recalls ECONO STERILE Medical Procedure Kits for Sterile Barrier Breach Risk
Sklar Instruments is recalling 245,015 ECONO STERILE medical procedure kits nationwide due to packaging issues that may compromise the sterile barrier. No illnesses or injuries have been reported.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE ROCH-PEAN FCP 8" CVD CS/25,Model Number 94-0286; 2) ECONO STERILE DRESSING FCP 5.5" CS/25LG,Model Number 94-0290; 3) ECONO STERILE TISSUE FCP 1X2 5.5" STER CS25,Model Number 94-0291; 4) ECONO STERILE FRCP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0944-2025·2025-01-22
Gynecological Speculum Kits Recalled for Potential Sterile Barrier Breach
Sklar Instruments is recalling ECONO STERILE gynecological speculum kits due to packaging issues that may compromise sterility. No injuries have been reported.
Product
ECONO STERILE medical procedure kits labeled as: 1) ECONO STERILE GRAVES SPEC STRL SM BX/25, Model Number 96-2603; 2) ECONO STERILE GRAVES SPEC STRL MD BX/25, Model Number 96-2605; 3) ECONO STERILE GRAVES SPEC STRL LG BX/25, Model Number 96-2607; 4) ECONO STERILE PEDER
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0869-2025·2025-01-22
Intuitive Surgical Fenestrated Grasper Recalled for Frayed or Broken Grip Cables
Intuitive Surgical is recalling its 8MM Tip-Up Fenestrated Grasper due to frayed or broken grip cables on reusable surgical instruments. The defect affects multiple batch numbers produced between 2023 and 2024.
Product
8MM,TIP-UP FENESTRATED GRASPER,IS4000¿ REF 470347
Category
Medical Device
Distribution
52 states
HighFDA (Devices)·Z-0916-2025·2025-01-22
Cardinal Health Presource Surgical Kits Recalled for Potential Endotoxin Contamination
Cardinal Health is recalling Presource surgical kits due to potential endotoxin contamination in non-sterile surgical strips and patties. The recall affects 512,786 units distributed worldwide.
Product
Cardinal Health Presource Kits: 1) ORTHO PLASTIC MICROVASCULAR PK , Catalog Number: PGVMFFBLY; 2) ORTHO PLASTIC MICROVASCULAR PK , Catalog Number: PGVMFFBLZ; 3) KIT,NEURO SPINE,ANDERSON , Catalog Number: PN23SPAM5; 4) KIT, MAJOR SPINE , Catalog Number: PN33MSOC3; 5) KIT, MAJOR
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0853-2025·2025-01-22
Surgical Forceps Recalled Due to Frayed or Broken Grip Cables
Intuitive Surgical is recalling 8,578 units of Cadiere Forceps surgical instruments due to reports of frayed or broken grip cables. These reusable instruments were distributed throughout the United States and internationally.
Product
8MM,CADIERE FORCEPS,IS4000 ¿ REF 470049
Category
Medical Device
Distribution
52 states
ModerateFDA (Drugs)·D-0204-2025·2025-01-22
Prescription Drug Cardura XL Recalled for Out-of-Specification Impurity
Viatris is recalling Cardura XL (doxazosin) 4 mg extended-release tablets nationwide due to out-of-specification impurity results detected during stability testing.
Product
CARDURA — CARDURA (DOXAZOSIN MESYLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0921-2025·2025-01-22
DRG:HYBRiD-XL Insulin Device Recalled for Calibration Failures
DRG International is recalling the DRG:HYBRiD-XL Insulin device (Model HYE-5361) due to calibration failures and out-of-specification controls that may delay assay results.
Product
DRG:HYBRiD-XL Insulin. Model/Catalog Number: HYE-5361
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0955-2025·2025-01-22
Demineralized Bone Matrix Putty Recalled for Incorrect Outer Box Expiration Date
IsoTis OrthoBiologics recalls OsteoSurge 100 Demineralized Bone Matrix Putty due to incorrect expiration dates on outer packaging. The outer box date does not match the correct date on the inner tray.
Product
OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix, OsteoSurge 100 Demineralized Bone Matrix, 10cc, REF 56300100.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0401-2025·2025-01-22
Eclectic Herb Vitamin Blend Dietary Supplement Recalled for Label Errors
Eclectic Herb Vitamin Herb Blend dietary supplement is recalled because the Supplement Facts panel contains incorrect ingredient names and quantities. Consumers should check affected lot numbers.
Product
Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement, 750mg, 150 capsules per plastic bottle, UPC 0 23363 52002 2. Eclectic Institute, Inc. 755 NE 6th Street Gresham, OR 97030. The affected label declared "Oregon Grape 190mg ***Oregon Grape 97mg***Cayenne Root (Allium
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0196-2025·2025-01-22
Acetaminophen Extra Strength tablets recalled for incorrect imprinting
Akron Pharma is recalling 1,232 bottles of Acetaminophen Extra Strength tablets due to incorrect imprinting on the tablets. The product identification may be wrong on the affected tablets.
Product
Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0195-2025·2025-01-22
Acetaminophen 325 mg tablets recalled for incorrect imprinting
Akron Pharma is recalling 14,825 bottles of Acetaminophen 325 mg tablets due to incorrect tablet imprinting affecting lots KDT0124004, KDT0124005, and KDT0124006 (expiring August 31, 2026). No illnesses have been reported.
Product
Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0919-2025·2025-01-22
OsteoCove and Cove Putty bone void fillers recalled due to hydration defect
IsoTis OrthoBiologics is recalling OsteoCove Putty and Cove Putty bone graft materials due to a hydration issue that makes the product less cohesive and moldable than intended.
Product
OsteoCove Putty, 1.25cc, REF 56920013 and Cove Putty, 1.25cc REF 02-9200-01.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0193-2025·2025-01-22
Acetaminophen Extra Strength tablets recalled for incorrect product imprint identification
Akron Pharma recalls 768 bottles of Acetaminophen Extra Strength 500 mg due to incorrect identification imprinted on the tablets nationwide.
Product
Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0942-2025·2025-01-22
Sklar Instruments ECONO STERILE Blackhead Extractor Kits Recall
Sklar Instruments is recalling ECONO STERILE blackhead extractor kits (Model 96-2395M) due to packaging issues that may compromise the sterile barrier. The kits were distributed nationwide.
Product
ECONO STERILE medical procedure kits labeled as: ECONO STERILE SCHAMBERG EXTRCT SQ STER CS25, Model Number 96-2395M; blackhead extractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0197-2025·2025-01-22
Diphenhydramine HCl Capsules Recalled Due to Wrong Imprinting
Akron Pharma is recalling Diphenhydramine HCl 25 mg capsules nationwide because the capsules are imprinted with incorrect identification. Consumers should stop using the affected product.
Product
Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8028-1.
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0198-2025·2025-01-22
Diphenhydramine HCl Capsules Recalled Due to Wrong ID Imprinting
Akron Pharma recalls 456 bottles of Diphenhydramine HCl 25 mg capsules due to incorrect ID imprinted on the capsules.
Product
Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W Building E., Suite 117, Fairfield, NJ 07004, NDC 71399-8028-2.
Category
Drug
Distribution
Distributed nationwide