State

Nevada product recalls

73,388 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total: 5,696
Critical: 951
Severe: 1,731
Most recent: 2026-09-25

Of the 5,696 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 1,731 (30%) are Severe.

Which agencies issued them

These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20226–20250 of 79084

SevereFDA (Food)·F-1609-2022·2022-09-07
Pediatric Nutrition Formula Recalled for Potential Bacterial Contamination
Kate Farms Pediatric Standard Sole-Source Nutrition Formula is recalled nationwide due to findings of potential Cronobacter sakazakii and Clostridium botulinum contamination.
Product
kate farms Pediatric Standard Sole-Source Nutrition Formula. 1.2 cal/mL. 250 ML (8.45 FL OZ) Tetra Pak container UPC 8 51823-00690 4. Sold in 12 count case UPC 00851823006997. Refrigerate after opening. Made for: Kate Farms, Inc., 101 innovation Place, Santa Barbara…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1649-2022·2022-09-07
Metalogix Self-Drill Half-Pin Surgical Component Recalled for Tip Breakage
New Standard Device Inc is recalling Metalogix Self-Drill Half-Pins used in external fixation surgery due to reports of tip breakages occurring during surgical procedures.
Product
Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill Half-Pin 5x30x215mm REF 620030 Metalogix Self-Drill Half-Pin 5x40x215mm REF 620040 Metalogix Self-Drill Half-Pin 5x60x215mm REF 620060…
Category
Medical Device
Distribution
11 states
HighFDA (Devices)·Z-1660-2022·2022-09-07
ARCHITECT STAT Troponin-I Reagent Kit Recalled for Insufficient Blocking Agents
Abbott is recalling one lot of ARCHITECT STAT Troponin-I Reagent Kits due to insufficient heterophilic blocking agents in the conjugate, which may affect test accuracy.
Product
ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1682-2022·2022-09-07
Sweetums Sucrose Solution Recalled for Contamination and Leaking Cups
Clinical Innovations is recalling Sweetums 24% Sucrose Solution used in NICU settings due to leaking cups and black particulates in the solution. The recall affects 1,773 boxes distributed nationwide.
Product
Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptically packaged in 15 mL cups with foil lid. Each cup contains 15 mL of USP purified water, 24% sugar, citric acid (buffer). Cup is latex-free, DEHP-free…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1647-2022·2022-09-07
Siemens Artis icono X-Ray Systems Recalled for Potential Hardware Failure
Siemens has recalled Artis icono X-ray imaging systems due to a potential hardware issue affecting a specific lot of X-ray tubes. If the error detection mechanism fails, the system cannot release X-rays until it is shut down.
Product
Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1648-2022·2022-09-07
Siemens Dimension Vista CA 15-3 Diagnostic Cartridges Recalled for Measurement Bias
Siemens Healthcare Diagnostics is recalling Dimension Vista CA 15-3 Flex reagent cartridges because the diagnostic test can produce inaccurate results, reading 26–33% lower than actual values, potentially delaying appropriate patient treatment decisions.
Product
Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3. Siemens Material Number (SMN)/Ref Catalog Number : 10464344/K6456
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1666-2022·2022-09-07
Radiographic imaging system may exceed radiation dose limits in biplane mode
Canon Medical's Alphenix i imaging systems may deliver radiation dose rates exceeding acceptable limits during biplane fluoroscopic procedures. Sixteen systems nationwide with software versions 8.0, 9.0, or 9.2 and TFP 1200C detector are affected.
Product
INFX-8000V. For radiographic and fluoroscopic studies and intervention.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V671000·2022-09-07
Nissan Titan vehicles recalled for transmission parking pawl failure risk
Nissan is recalling 2020-2023 Titan vehicles and certain other models because the transmission parking pawl may fail to engage in park, risking vehicle rollaway and crash.
Product
NISSAN — NISSAN TITAN, FRONTIER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1684-2022·2022-09-07
Clinical Innovations Sweetums Sucrose Solution Vials Recalled for Contamination
Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to complaints of leaking, black liquid, and black particulates in product vials. The recall affects neonatal products distributed nationwide and internationally.
Product
Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1645-2022·2022-09-07
X-Ray Imaging System X-Ray Tube Hardware Defect Worldwide Recall
Siemens has recalled Artis Q and Artis Q.zen X-ray imaging systems due to a potential X-ray tube hardware defect. In rare cases, if error detection fails, the system will not be able to release X-ray until shut down; 1,389 units are affected globally.
Product
Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis Q.zen floor- Model No. 10848353 Artis Q.zen ceiling- Model No. 10848354 Artis Q.zen biplane- Model No. 10848355
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1468-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste Recalled for Improper Storage Conditions
Family Dollar is recalling Colgate OPTIC WHITE CHARCOAL COOL MINT toothpaste (Net Weight 4.2 oz., UPC 0 35000 97872 1) distributed to stores in 11 states due to improper temperature storage during manufacturing.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V670000·2022-09-07
BMW X7 Third-Row Seat Backrest Springs May Not Lock Properly
BMW is recalling 2019-2022 X7 models with third-row seats because compression springs may not have been properly installed, causing the seat backrest to potentially fail to lock in a crash.
Product
BMW — BMW X7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1563-2022·2022-09-07
Philips Radiography System Firmware Defect Risks Incorrect Radiation Dose
Philips DigitalDiagnost C50 1.1 radiography systems contain a firmware defect in the Wallstand VS2 board that may cause incorrect radiation dose and anatomic marker misalignment. Eleven affected systems were distributed nationwide.
Product
DigitalDiagnost C50 1.1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1685-2022·2022-09-07
Sucrose solution vials recalled nationwide for contamination and leaking
Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to reports of leaking containers and contamination with black liquid and particulates. The product is used in hospital settings including neonatal intensive care units.
Product
Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1465-2022·2022-09-07
Colgate OPTIC WHITE PRO Series Toothpaste Recalled for Improper Storage
Family Dollar Stores is recalling 1,120 packages of Colgate OPTIC WHITE PRO SERIES toothpaste due to improper temperature storage conditions that deviate from cGMP standards.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0 35000 99658 9. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1473-2022·2022-09-07
Prescription Antibiotic Tablets Recalled for Foreign Matter in Active Ingredient
Teva Pharmaceuticals is recalling Neomycin Sulfate Tablets because teflon was found in the active ingredient. Affected lot numbers: 3007830, 3007746, 3007829.
Product
NEOMYCIN SULFATE — NEOMYCIN SULFATE (NEOMYCIN SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1466-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste recalled for improper storage conditions
Colgate Anticavity Fluoride Toothpaste, Optic White Renewal was recalled after being stored outside appropriate temperature conditions. The recall affects 840 packages distributed to Family Dollar stores in 11 states.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITTE RENEWAL, 3% Hydrogen Peroxide, High Impact White, Net Wt. 3.0 OZ. (85 g) UPC 0 35000 97008 4. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1470-2022·2022-09-07
Colgate OPTIC WHITE Mouthwash Recalled Due to Improper Storage Conditions
Family Dollar is recalling Colgate Whitening Mouthwash OPTIC WHITE ICY FRESH MINT due to temperature storage deviations. 840 packages were distributed to Family Dollar stores in multiple states.
Product
Colgate Whitening Mouthwash, OPTIC WHITE ICY FRESH MINT. 16 fl. OZ. (1 pt) 473 mL UPC 0 35000 67111 0. Dist. by: Colgate-Palmolive Co. New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1668-2022·2022-09-07
DeRoyal Sterile Custom Kits Recalled for Defective Connectors
DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors are being recalled because the procedure packs contained a recalled product. Approximately 1,306 kits were distributed in Ohio and Tennessee.
Product
DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear Connectors
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1471-2022·2022-09-07
Timolol Maleate eye drops recalled for unknown impurity in stability testing
Akorn, Inc. is recalling Timolol Maleate Ophthalmic Solution due to identification of an unknown impurity during 12-month stability testing. No illnesses have been reported.
Product
Timolol Maleate Ophthalmic Solution, USP, 0.5%, 5 x 0.3 mL Single-Dose Vials, Rx Only, Sterile, Manufactured for: Akorn, Inc., Lake Forest, IL 60045. NDC 17478-189-24
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1467-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste recalled for improper storage conditions
Colgate Anticavity Fluoride Toothpaste OPTIC WHITE ADVANCED ICY FRESH is recalled due to improper temperature storage during manufacturing. Approximately 1,680 packages distributed across 11 U.S. states are affected.
Product
Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE ADVANCED ICY FRESH, Net Wt. 3.2 OZ. (90 g) UPC 0 35000 97159 3. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1472-2022·2022-09-07
Nighttime Sleep-Aid tablets recalled due to carton labeling error
CVS Pharmacy is recalling Nighttime Sleep-Aid tablets because the carton incorrectly identifies the active ingredient as doxylamine succinate HCl instead of doxylamine succinate. Approximately 257,064 cartons were distributed nationwide.
Product
Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count blisters per carton, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895, UPC 0 50428 34873 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1497-2022·2022-09-07
Triamcinolone Acetonide Cream Recalled for Manufacturing Defects
Padagis US LLC is recalling 57,816 tubes of Triamcinolone Acetonide Cream 0.1% nationwide due to manufacturing process deviations. Consumers reported gritty texture and reduced effectiveness.
Product
TRIAMCINOLONE ACETONIDE — TRIAMCINOLONE ACETONIDE (TRIAMCINOLONE ACETONIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1646-2022·2022-09-07
X-ray imaging system hardware defect may prevent operation
Siemens is recalling certain X-ray imaging systems due to a potential hardware issue with the error detection mechanism. In rare cases, this could prevent X-ray emission until system shutdown.
Product
Artis pheno- Model No. 10849000
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1469-2022·2022-09-07
Colgate Anticavity Fluoride Toothpaste Recalled Due to Improper Storage Conditions
Family Dollar Stores recalls 1,400 packages of Colgate Anticavity Fluoride Toothpaste due to improper temperature storage conditions during manufacturing. The product may not meet quality standards.
Product
Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER CLEAN MINT PASTE. Net Wt. 4.2 OZ. (119 g) UPC 0 35000 45836 0. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
Category
Drug
Distribution
Distributed nationwide