State

Nevada product recalls

72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3251–3275 of 78628

HighFDA (Devices)·Z-1334-2026·2026-02-18
Dressing change trays recalled over open swabstick applicator seals
Medline is recalling 8,445 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Product
Medline medical convenience kits packaged as: ) LVAD DRESSING CHANGE TRAY, Kit SKU DM320C; 2) PORT AND IO ACCESS DRESSING KI, Kit SKU DT15780A; 3) PORT-A-CATH DRESSING CHANGE TR, Kit SKU DT16615; 4) LARGE BORE CENTRAL LINE DRSG C, Kit SKU DT19660; 5) CENTRAL LINE DRESS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1351-2026·2026-02-18
Azurion 5 M20 systems recalled over tables that may move unexpectedly
Philips is recalling 922 units of the Azurion 5 M20 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1348-2026·2026-02-18
Azurion 7 M12 systems recalled over tables that may move unexpectedly
Philips is recalling 1 of the Azurion 7 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0331-2026·2026-02-18
Testosterone and anastrozole pellets recalled over potential metal particulate
Asteria Health is recalling 1,464 pellets of Testosterone 100mg, Anastrozole 4mg sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone 100mg Anastrozole 4mg , 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4104-32
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0338-2026·2026-02-18
Oxycodone blister cards recalled over seals that let tablets fall out
Amerisource Health Services is recalling 31,676 packages of Oxycodone Hydrochloride Tablets 5 mg over card seal defects that let tablets fall out of their cavities.
Product
OXYCODONE HYDROCHLORIDE — OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0313-2026·2026-02-18
Estradiol 22mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 133 pellets of ESTRADIOL, 22 mg sterile pellets over the potential presence of metal particulate matter.
Product
ESTRADIOL, 22 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3022-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1327-2026·2026-02-18
Catheter securement dressing kits recalled over open swabstick seals
Medline is recalling 1,350 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Product
Medline medical convenience kits packaged as: ADULT CATH SECUREMENT DRSG, Kit SKU DYNDC3109
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0492-2026·2026-02-18
Tater tots recalled over small hard plastic fragments in product
McCain Foods USA is recalling 21,557 cases of Ore-Ida Tater Tots shaped potatoes over foreign material described as small hard plastic fragments.
Product
Ore-Ida Tater Tots shaped potatoes, item number OIF00215A. Frozen potato product is packaged in clear unlabeled poly bag (6/5 lb bags), Net Wt. 30 lbs (13.6 kg)/ case. UPC on 30 lbs case label: 1 00 72714 00215 8. Manufactured by McCain Foods USA Inc. McCain distributed this pro
Category
Food
Distribution
28 states
HighFDA (Devices)·Z-1333-2026·2026-02-18
Blood culture kits recalled over open swabstick applicator seals
Medline is recalling 4,300 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Product
Medline medical convenience kits packaged as: BLOOD CULTURE KIT NS, Kit SKU DYNDH2088
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0325-2026·2026-02-18
Testosterone 303mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 1,015 pellets of Testosterone, 303 mg sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone, 303 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1303-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0336-2026·2026-02-18
Vancomycin injection bags recalled over a lack of assurance of sterility
Fresenius Kabi Compounding is recalling 1,578 bags of Vancomycin HCl injection over a lack of assurance of sterility.
Product
vancomycin HCl, 1.5 grams, 1.5 grams added to 500 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-016-59
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1315-2026·2026-02-18
Brilliance iCT scanners recalled over rotor fasteners that may be undertorqued
Philips is recalling 47 units of the Brilliance iCT because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Product
Brilliance iCT; Product Code (REF): 728306;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1339-2026·2026-02-18
GammaPlan 11.1 recalled over plans that may irradiate the wrong location
Elekta is recalling Leksell GammaPlan version 11.1 because an error when defining a new stereotactic reference may produce a treatment plan that irradiates the incorrect patient location.
Product
Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment planning system Software Version: 11.1 Product Description: Leksell GammaPlan¿ is a computer-based system designed for Leksell Gamma Knife¿ treatment planning.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0308-2026·2026-02-18
Estradiol 10mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 24,099 pellets of ESTRADIOL, 10 mg sterile pellets over the potential presence of metal particulate matter.
Product
ESTRADIOL, 10 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3010-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1313-2026·2026-02-18
Adult intubation trays recalled over a smaller catheter packed inside
Medline is recalling 130 Adult Intubation Trays because an 8 Fr suction catheter may have been packed in place of the required 14 Fr catheter.
Product
Intubation Tray (Adult) containing Suction Catheter Kits SKU DYNJAA245B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1335-2026·2026-02-18
Sterile resuture packs recalled over open swabstick applicator seals
Medline is recalling 216 kits of convenience kits containing BD ChloraPrep Triple Swabsticks, which BD determined may exhibit an open seal on the applicator packaging.
Product
Medline medical convenience kits packaged as: STERILE RESUTURE PACK, Kit SKU DYNDL1980A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0496-2026·2026-02-18
Movie house popcorn recalled because it may contain foreign material
Lee's Commissary is recalling 6,480 packages of Red Button Movie House Popcorn, 24 oz, because the product may contain foreign material.
Product
Brand: Red Button Movie House Popcorn Pack Size: 24 oz. / 680g. SKU/UPC:4117281332 Shelf life: 150 days. Packaging: Plastic bag Production location: Lee s Commissary 888 W 1600 S Unit 130, Logan Ut. 84321 Distributed by: Associated Food Stores
Category
Food
Distribution
8 states
HighFDA (Devices)·Z-1344-2026·2026-02-18
Azurion 3 M12 systems recalled over tables that may move unexpectedly
Philips is recalling 291 units of the Azurion 3 M12 because the table may move unexpectedly when the Reset Geometry button is pressed, even with a table lock active.
Product
Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0493-2026·2026-02-18
Sonic Tots recalled over small hard plastic fragments in product
McCain Foods USA is recalling 67 cases of Sonic Tots frozen potato product over foreign material described as small hard plastic fragments.
Product
Sonic Tots, item number SON00543. Frozen potato product is packaged in clear unlabeled poly bags (6/5 lb), Net Wt 30 lbs (13.61 kg)/ case. UPC 0 00 72714 00543 5. Manufactured By: McCain Foods USA Inc. Oakbrook Terrace, IL.
Category
Food
Distribution
28 states
HighFDA (Drugs)·D-0316-2026·2026-02-18
Testosterone 12.5mg pellets recalled over potential metal particulate matter
Asteria Health is recalling 3,871 pellets of Testosterone, 12.5 mg sterile pellets over the potential presence of metal particulate matter.
Product
Testosterone, 12.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1012-32.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1317-2026·2026-02-18
Spectral CT scanners recalled over rotor fasteners that may be undertorqued
Philips is recalling 283 Spectral CT units because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.
Product
Spectral CT; Product Code (REF): 728333;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1338-2026·2026-02-18
Transport bag kits recalled over a Tyvek bag seal issue
AVID Medical is recalling 1,500 Halyard Transport Bag Kits because a Tyvek bag seal issue may compromise the sterility of the kit.
Product
Halyard TRANSPORT BAG KIT. Kit Code: LIFE0080-01.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1343-2026·2026-02-18
Spinal navigation instruments recalled over incorrect array connection geometry
Alphatec Spine is recalling 15 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Product
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 267-01-000-10-N UDI-DI code: 00190376541471; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1342-2026·2026-02-18
Navigation osteotomes recalled over incorrect array connection geometry
Alphatec Spine is recalling 7 ATEC Lateral Navigation Disc Prep Instruments due to a design issue where the navigated array connection geometry is incorrect.
Product
ATEC Lateral Navigation Disc Prep Instruments LIF NAV, OSTEOTOME 10mm REF 266-01-000-10-N UDI-DI code: 00190376476179; GMDN 12844 The ATEC Navigation Disc Prep Instruments are intended for use in surgical procedures. These instruments are non-sterile or sterile packaged, re-
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1361-2026·2026-02-18
Display adapters recalled after the wrong configuration file was used
Steris is recalling 10 units of the Barco MNA with HexaVue IP Integration System because the supplier used the incorrect configuration file for a limited batch of adapter components.
Product
Barco MNA with the HexaVue IP Integration System, Model/Catalog Number: MNA-6x0-H
Category
Medical Device
Distribution
Distributed nationwide