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.

8501–8525 of 78685

SevereFDA (Food)·F-0358-2025·2025-01-08
Organic Baby Carrots Recalled Due to E. coli Contamination Risk
Grimmway Farms is recalling organic baby carrots sold under multiple brands due to potential E. coli O121:H19 contamination affecting approximately 218,705 cases distributed nationwide and internationally.
Product
--- Organic Baby Carrots --- Orangic Baby Peeled Carrots 13/3 BL; Orangic Baby Peeled Carrots 30/1 BL; Org Baby Peeled Carrots 12/2 Wholesome Pantry RPC; Org Baby Peeled Carrots 24/1 Wholesome Pantry RPC; Organic Baby Peeled Carrots 10/2/2Lb Cal O Display; Organic Baby Peeled Car
Category
Food
Distribution
41 states
SevereFDA (Food)·F-0434-2025·2025-01-08
Cascade Raw Cheddar Cheese Recalled Due to E. Coli Contamination
Heber Valley Artisan Cheese is recalling Cascade Raw Cheddar Cheese due to Shiga toxin-producing E. coli (STEC) and elevated E. coli detected in finished products. The affected cheese was sold in MT, NV, UT, and WY.
Product
Cascade Raw Cheddar GTIN #90854115003059 packed in an approximately 6 lb quarter wheels vacuum sealed. All quarter wheels are variable weight sold by the pound and each vacuum sealed package contains 1 quarter wheel.
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0361-2025·2025-01-08
Organic Whole Carrots Recalled for Potential E. coli O121:H19 Contamination
Grimmway Farms is recalling approximately 4,057 cases of organic whole carrots distributed nationally due to potential E. coli O121:H19 contamination. No illnesses have been reported.
Product
--- Organic Whole Carrots --- Organic Clip Carrots 50 Lbs Cal-Organic Farm; Organic Clip Carrots 50 Lbs Cal-Organic RPC --- Brand --- Cal-Organic
Category
Food
Distribution
41 states
SevereFDA (Food)·F-0373-2025·2025-01-08
Fresh cucumbers recalled due to potential Salmonella contamination
Baloian Farms is recalling fresh cucumbers sold under the Pamela and Stock Vegetables brands due to potential Salmonella contamination. Approximately 40,043 cases were distributed to wholesale, retail, and food service operations across 18 states.
Product
whole fresh American cucumbers packaged in bulk cardboard containers labeled with the "Pamela" brand, a generic white box with a sticker that provides the implicated grower's name, "Agrotato, S.A. de C.V.," or a clear PamPak branded bag of 6 individual cucumbers with the UPC 8 25
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-0776-2025·2025-01-08
Baxter Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter Healthcare is recalling certain infusion pumps that were released after repair without complete testing. Incomplete testing could affect how the device delivers medication to patients.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8), Product Code 35700BAX2
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2025·2025-01-08
Baxter SIGMA Spectrum Infusion Pump Recalled for Incomplete Post-Repair Testing
Baxter is recalling SIGMA Spectrum Infusion Pump (Version 6) units that were released after repair without complete flow testing. The incomplete testing poses a risk of improper device operation.
Product
Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6), Product Code 35700BAX
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·25087·2025-01-08
SIG SAUER ROMEO5 Red Dot Firearm Sights Recalled Due to Button Battery Ingestion Hazard
SIG SAUER recalled about 230,000 ROMEO5 red dot sights because the included button cell battery can be easily accessed and lacks required child-resistant packaging, posing a serious ingestion hazard to children.
Product
SIG SAUER ROMEO5 Red Dot Sights
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0774-2025·2025-01-08
SynchroMed II and III Implantable Pumps Recalled for Software Issues
Medtronic has recalled 3,981 SynchroMed implantable pumps worldwide due to software issues in application version 2.x used to program the devices.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900E CLINICIAN TABLET GLBL SMSNG and PROG CT900E CLINICIAN TABLET PAPER EN with the A810 CP app version 2.x, CFN CT900E
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·25088·2025-01-08
Children's Bike Helmets Recalled for Failure to Meet Federal Safety Standards
About 6,500 Wemfg children's bike helmets sold on Amazon fail to comply with federal safety standards for impact protection and stability. The helmets can fail to protect in crashes, posing a risk of head injury.
Product
Wemfg Children's Multi-Purpose Bike Helmets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0783-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Non-Sterile Components
Medline is recalling 943 custom surgical kits containing non-sterile Codman Surgical Patties and Strips that may be contaminated with endotoxin.
Product
Medline custom medical procedure kits labeled as: 1) FREE FLAP BASIC SET-UP PK, REF DYNJ0991320J; 2) MVFF/FIBU #54-RF, REF DYNJ21927R; 3) FUNCTIONAL SINUS ENDOSCOPY, REF DYNJ40406A; 4) DR GOLDSTEIN ACCESSORY PACK, REF DYNJ51818F; 5) ENDOSCOPIC SKULL BASE, REF DYNJ58648
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2025·2025-01-08
Medline Surgical Procedure Kits Recalled for Endotoxin Contamination Risk
Medline Industries is recalling 2344 custom surgical kits with non-sterile components that may contain endotoxins. The kits were distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) OPEN HEART CDS-LF, REFCDS840451M; 2) NEURO PACK, REFDYNJ41516M; 3) RFD- AAA PACK, REFDYNJ54242B; 4) OPEN HEART A&B, REFDYNJ901203C; 5) OPEN HEART A&B, REFDYNJ901203D; 6) ACDF-LF, REFDYNJ906681B; 7) ACDF-LF, REFDY
Category
Medical Device
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-01082025-01·2025-01-08
Chicken Curry Empanadas Recalled For Undeclared Milk Allergen
USDA FSIS issued a public health alert for Chicken Curry Empanadas that may contain undeclared milk. Consumers with milk allergies should not consume these products.
Product
Rajbhog Foods (NJ), Inc. — FSIS Issues Public Health Alert For Chicken Empanada Products Due To Misbranding And Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0797-2025·2025-01-08
3M Unitek Orthodontic Primer Recalled Due to Bond Failures and Skin Irritation
3M Unitek is recalling Transbond Plus Self-Etching Primer used in orthodontic bonding due to reports of bracket bond failures and skin irritation or blistering.
Product
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self Etching Primer is an orthodontic all-in-one etchant and primer that is used in the bonding process of orthodontic appliances to teeth.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0782-2025·2025-01-08
Medical Device Kits Recalled for Non-Sterile Surgical Components
Medline Industries is recalling See DocMan custom convenience kits that contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. Approximately 48,655 units were distributed worldwide.
Product
See DocMan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0780-2025·2025-01-08
Medline custom surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline custom procedure kits containing non-sterile Codman Surgical Patties & Strips are being recalled due to potential endotoxin contamination. The recall affects 74 units distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER SUPPLEMENT, REF DYNJ69476; 2) DIEP FLAP, REF DYNJ910120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0794-2025·2025-01-08
Medline surgical procedure kits recalled for non-sterile components and endotoxin contamination
Medline is recalling 474,300 custom surgical procedure kits because they contain non-sterile Codman Surgical Patties and Strips with potential endotoxin contamination. These components could pose infection risks during surgical procedures.
Product
Medline custom medical procedure kits labeled as: 1) CRANI, REF CDS780089V; 2) CRANIOFACIAL CDS, REF CDS780102K; 3) CRANIOFACIAL CDS, REF CDS780102L; 4) CRANIOFACIAL CDS, REF CDS780102M; 5) CRANIOTOMY CDS-LF, REF CDS780105K; 6) CRANIOTOMY CDS-LF, REF CDS780105L; 7) CRANIO
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0365-2025·2025-01-08
Sam's Club Hatch Chile Chicken Enchiladas Recalled for Listeria
Sam's Club is recalling Member's Mark Hatch Chile Chicken Enchiladas because the product may contain Listeria monocytogenes.
Product
Member's Mark Hatch Chile Chicken Enchiladas, ready to cook, perishable, packaging type: aluminum/black oven-safe tray Net wt. variable - average 1.52 lbs. UPC 00226529000004, UPC 00409802813793
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0786-2025·2025-01-08
Medline Custom Surgical Kits Recalled for Non-Sterile Components with Endotoxin Risk
Medline Industries is recalling 3,903 custom medical procedure kits due to non-sterile Codman Surgical Patties and Strips with potential for endotoxin contamination. The recall affects products distributed in the US, UAE, and Canada.
Product
Medline custom medical procedure kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, REF DYNJ0660040R; 2) FREE FLAP PACK-LF, REF DYNJ42833A; 3) FREE FLAP PACK-LF, REF DYNJ42833B; 4) TYMPANOPLASTY PACK, REF DYNJ50692C; 5) MAJOR CRANIOTOMY SAFETY, REF DYNJ54736B; 6) FREE FLAP CU
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0173-2025·2025-01-08
Ketamine injection syringes recalled due to missing tamper-evident seals
Hikma Injectables is recalling 1,800 ketamine injection syringes nationwide because tamper-evident seals are not attached to several syringes, compromising sterility assurance.
Product
ketamine inj 50 mg per 1 mL, Rx Only, 1 mL fill in a 3mL pre-filled syringe, For IV or IM Use, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, This is a Compounded Drug. Hospital/Office Use Only. NDC 63037-137-25
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0773-2025·2025-01-08
Medtronic Implantable Drug Pumps Recalled for Software Defects
Medtronic has recalled 566 SynchroMed II and III implantable drug infusion pumps due to software issues in the controlling application. No injuries or illnesses have been reported.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900D CLINICIAN TABLET GLOBAL with the A810 CP app version 2.x, CFN CT900D
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0772-2025·2025-01-08
SynchroMed II and III implantable pumps recalled for software issues
Medtronic recalled SynchroMed II and III implantable pumps for software issues in the clinician tablet application. Fifty-nine systems are affected.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900C CLINICIAN TABLET UK with the A810 CP app version 2.x, CFN CT900C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0785-2025·2025-01-08
Medline surgical procedure kits recalled for potential endotoxin contamination
Medline is recalling three custom surgical procedure kits due to non-sterile Codman Surgical Patties and Strips that pose a potential endotoxin contamination risk. The affected kits were distributed in the US, Canada, and the UAE.
Product
Medline custom medical procedure kits labeled as: 1) PANENDOSCOPY-LF, REF DYNJ36728C; 2) ENDOSCOPIC SINUS PACK, REF DYNJ40644A; 3) ENDO SINUS PACK, REF DYNJ66449.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2025·2025-01-08
Medtronic SynchroMed II and III Implantable Pumps Recalled for Software Defects
Medtronic is recalling SynchroMed II and III implantable pumps used with a clinician tablet app that has software issues in version 2.x. Approximately 319 systems were distributed worldwide.
Product
SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable pumps used with PROG CT900B CLINICIAN TABLET EU -UK with the A810 CP app version 2.x, CFN CT900B
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V003000·2025-01-08
Blue Bird Recalls 2024-2025 All American School Buses for Wiring Defect
Blue Bird is recalling 2024-2025 All American school buses because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V004000·2025-01-08
Blue Bird Recalls 2025 All American Bus for Wiring Defect
Blue Bird is recalling one 2025 All American transit bus because incorrect wiring reverses high and low beams, potentially blinding other drivers.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide