State

Nevada product recalls

72,984 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: 2026-09-09

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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6601–6625 of 78676

SevereFDA (Food)·F-0897-2025·2025-06-11
Fresh Take Crave Away Italian Hoagie Sub Sandwich Listeria Recall
Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Italian Hoagie Sub Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The affected products were distributed to the Southwest and military facilities.
Product
Fresh Take Crave Away Italian Hoagie Sub Sandwich; 6oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 61440 4
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0848-2025·2025-06-11
Fresh & Ready Foods Thai Chicken Ciabatta Sandwich Listeria Recall
Fresh & Ready Foods LLC is recalling Thai Chicken on Ciabatta Sandwiches due to Listeria Monocytogenes detected on food contact surfaces at the manufacturing facility. The recall affects 139,863 units distributed across the Southwest.
Product
Fresh & Ready Foods Thai Chicken on Ciabatta Sandwich, 9 oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 90877 4
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0885-2025·2025-06-11
Turkey & Cheese Sandwiches Recalled for Listeria Contamination Risk
City Point Market Fresh Food to Go Turkey & Cheese on Wheat Sandwiches are being recalled due to detection of Listeria Monocytogenes on food contact surfaces at the manufacturing facility. The product was distributed to government and military facilities in California, Nevada, Arizona, and Washington.
Product
City Point Market Fresh Food to Go Turkey & Cheese on Wheat Sandwich 5.5oz, PLASTIC CONTAINER Best By: 05/09/2025 - 05/18/2025 UPC# 4 00694 44186 6
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0857-2025·2025-06-11
Fresh & Ready Foods Ham & Cheese Mega Sandwich Recalled for Listeria
Fresh & Ready Foods LLC is recalling Ham & Cheese Mega Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The recall affects approximately 139,863 units distributed to the Southwest and military facilities.
Product
Fresh & Ready Foods Ham & Cheese Mega Sandwich, 7.5oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89048 2
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0881-2025·2025-06-11
Fresh & Ready Foods Chicken Salad Sandwich Recalled for Listeria
Fresh & Ready Foods is recalling Chicken Salad on Wheat Sandwiches (4.5oz) due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The affected products were distributed to retailers and military facilities in California, Nevada, Arizona, and Washington.
Product
Fresh & Ready Foods Chicken Salad on Wheat Sandwich, 4.5oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89054 3
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0864-2025·2025-06-11
Fresh & Ready Foods Turkey Bacon Club Sandwich Recalled for Listeria
Fresh & Ready Foods is recalling Turkey & Bacon Club Multigrain Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The recall affects products with best-by dates of 05/09/2025–05/12/2025.
Product
Fresh & Ready Foods Turkey & Bacon Club Multigrain Sandwich, 6oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89064 2
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0909-2025·2025-06-11
Fresh Take Crave Away Turkey Bacon Club Sandwich Recalled for Listeria
Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Turkey & Bacon Club Multigrain Sandwiches (6.5oz containers, Best By 05/09/2025–05/19/2025) because Listeria monocytogenes was detected on food contact surfaces in the manufacturing facility.
Product
Fresh Take Crave Away Turkey & Bacon Club Multigrain Sandwich; 6.5oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 85889 9
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0917-2025·2025-06-11
Fresh Take Crave Away Egg Salad Sandwich Recalled for Listeria Risk
Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Egg Salad on Wheat Sandwiches because Listeria monocytogenes was detected on food contact surfaces at the manufacturing facility.
Product
Fresh Take Crave Away Egg Salad on Wheat Sandwich; 5oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 58575 5
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0876-2025·2025-06-11
Fresh & Ready Foods Tuna Salad Sandwich Recalled for Listeria Risk
Fresh & Ready Foods LLC is recalling Tuna Salad on Wheat Sandwiches (4.5 oz) after Listeria Monocytogenes was detected on food contact surfaces at the manufacturing facility. The product was distributed to Southwest locations and Government (Military) facilities.
Product
Fresh & Ready Foods Tuna Salad on Wheat Sandwich, 4.5oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89053 6
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0859-2025·2025-06-11
Fresh & Ready Foods Turkey Cranberry Multigrain Sandwich Recall
Fresh & Ready Foods LLC is recalling Turkey Cranberry Multigrain Sandwiches (7oz containers, UPC 6 82906 89296 7) due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility.
Product
Fresh & Ready Foods Turkey Cranberry Multigrain Sandwich, 7oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89296 7
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0896-2025·2025-06-11
Fresh Take Crave Away Club Supreme Sub Sandwich recall for Listeria
Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Club Supreme Sub Sandwich due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility.
Product
Fresh Take Crave Away Club Supreme Sub Sandwich; 6oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 61439 8
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0849-2025·2025-06-11
Fresh & Ready Foods Turkey & Cheese Croissant Sandwich Recalled
Fresh & Ready Foods LLC is recalling Turkey & Cheese Croissant Sandwiches due to Listeria monocytogenes detected on food contact surfaces at the manufacturing facility. The product was distributed to facilities in CA, NV, AZ, and WA.
Product
Fresh & Ready Foods Turkey & Cheese Croissant Sandwich, 6 oz. plastic container. Best buy: 05/09/2025-05/12/2025 UPC# 6 82906 89293 6
Category
Food
Distribution
4 states
SevereFDA (Food)·F-0913-2025·2025-06-11
Fresh Take Crave Away Ham & Cheese Sub recalled for Listeria contamination risk
Fresh & Ready Foods LLC is recalling Fresh Take Crave Away Ham & Cheese Sub sandwiches due to Listeria Monocytogenes detected on food contact surfaces at the manufacturing facility. The product was distributed to facilities in California, Nevada, Arizona, and Washington.
Product
Fresh Take Crave Away Ham & Cheese Sub; 6oz PLASTIC CONTAINER; Best By: 05/09/2025 - 05/19/2025 UPC# 8 06795 58569 8
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1896-2025·2025-06-11
Signature Laparoscopic Sharp Tooth Grasper Insulation Defect Recall
Silex Medical recalls the Signature Laparoscopic Sharp Tooth Grasper due to incomplete insulation on the shaft near the rotator wheel, which creates an electrical hazard during use.
Product
Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863020.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V387000·2025-06-11
Rivian R1S and R1T front turn signals may fail to illuminate
Rivian is recalling certain 2025 R1S and R1T vehicles because one or both front turn signals may fail to illuminate and flash, failing FMVSS 108. 27,882 units affected.
Product
RIVIAN — RIVIAN R1S, R1T
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1887-2025·2025-06-11
Palindrome Precision SI Chronic Hemodialysis Catheter Sterile Barrier Recall
Mozarc Medical US LLC is recalling Palindrome Precision SI Chronic Hemodialysis Catheters (Sport Pack) due to a potential breach of sterile barrier packaging. Approximately 95,938 units distributed nationwide and in Canada and Mexico are affected.
Product
Palindrome Precision SI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1886-2025·2025-06-11
Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack Recalled
Mozarc Medical is recalling Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Packs due to a potential breach of sterile barrier packaging that could compromise the catheter's sterility.
Product
Palindrome Precision HSI Chronic Hemodialysis Catheter Sport Pack. Radiopaque urethane catheter.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0928-2025·2025-06-11
GNC Women's 30+ Vitapak recalled due to undeclared fish allergen
GNC Holdings LLC is recalling GNC Women's 30+ Vitapak due to undeclared fish allergen (parvalbumin). The product was distributed across multiple states.
Product
GNC Women's 30+ Vitapak, Carton of 30 Sachets. Each sachet contains four tablets and a capsule. Paper-board carton that measures 10.25 width x 3.56 height x 3.15 depth containing 30 sachets of 3 width x 2.75 height with tear notch. 15 Cartons per Case
Category
Food
Distribution
48 states
HighFDA (Devices)·Z-1900-2025·2025-06-11
Signature Laparoscopic Atraumatic Grasper Insulation Defect Recall
Silex Medical is recalling Signature Laparoscopic Instruments (Model 5881033) because insulation on the shaft does not fully extend to the proximal end, leaving an exposed area near the rotator wheel.
Product
Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5881033.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1911-2025·2025-06-11
Olympus EVIS EXERA III Duodenovideoscope TJF-Q190V Contamination Risk
Olympus is recalling the EVIS EXERA III Duodenovideoscope Model TJF-Q190V due to post-market data showing higher microbial contamination when manual cleaning is delayed beyond one hour after patient use.
Product
Olympus EVIS EXERA III Duodenovideoscope. Model Number: TJF-Q190V
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0455-2025·2025-06-11
Fluoxetine Tablets USP 20 mg Recalled for N-Nitroso Contamination
Torrent Pharma Inc. is recalling Fluoxetine Tablets USP 20 mg due to the presence of N-Nitroso Fluoxetine exceeding the interim acceptable intake limit. The affected lot is distributed nationwide.
Product
FLUOXETINE — FLUOXETINE (FLUOXETINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1899-2025·2025-06-11
Signature Laparoscopic Atraumatic Grasper Instrument Insulation Defect Recall
Silex Medical is recalling Signature Laparoscopic Atraumatic Grasper instruments (Model 5864000) due to incomplete insulation on the shaft that leaves an exposed area near the rotator wheel, posing an electrical safety risk during surgical use.
Product
Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5864000.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1893-2025·2025-06-11
Signature Laparoscopic Dolphin Nose Grasper Instrument Insulation Defect
Silex Medical is recalling 2 units of a Signature Laparoscopic Instruments Dolphin Nose Grasper with Rotating Shaft due to incomplete insulation on the shaft, leaving an exposed area near the rotator wheel.
Product
Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5860020.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1898-2025·2025-06-11
Signature Laparoscopic Alligator Grasper Instrument Recall Safety Issue
Silex Medical is recalling the Signature Laparoscopic Alligator Grasper with Rotating Shaft (Model 5863050) because insulation on the tube does not fully extend to the proximal end of the shaft, leaving an exposed uninsulated area near the rotator wheel.
Product
Signature Laparoscopic Instruments, Alligator Grasper with Rotating Shaft and Monopolar Electrosurgical Footswitch Connector. Model/REF Number: 5863050.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1908-2025·2025-06-11
Beckman Coulter Sample Probes with Defective Tips Clinical Chemistry
Beckman Coulter is recalling sample probes with defective tips used in clinical chemistry analyzers. The defective probes may dispense lower sample concentrations, potentially leading to false low test results and delayed diagnosis.
Product
Sample probe sucks a sample dispensed into a tube or cup and discharges the appropriate amount into a cuvette. Lot 178713114 - 179433670
Category
Medical Device
Distribution
Distributed nationwide