The Recall Desk

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.

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.

3201–3225 of 78628

  • CriticalFDA (Devices)·Z-1324-2026·2026-02-18

    Reprocessed ultrasound catheters recalled over residual material particles inside

    Medline is recalling 94 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH; Bios
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1323-2026·2026-02-18

    Reprocessed ViewFlex ICE catheters recalled over residual material particles

    Medline is recalling 650 units because these lots of reprocessed catheters may contain small particles of residual material.

    Product
    Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0353-2026·2026-02-18

    UDENYCA syringes recalled after cartons were stored at room temperature

    McKesson is recalling 116 cartons of UDENYCA pegfilgrastim-cbqv injection because they were stored in a controlled room temperature environment instead of the required refrigerated environment.

    Product
    UDENYCA — UDENYCA (PEGFILGRASTIM-CBQV)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0491-2026·2026-02-18

    Mini beignets recalled over undeclared hazelnut in the filled product

    Costco Wholesale is recalling 8,073 packages of Kirkland Signature Mini Beignets filled with Caramel over undeclared hazelnut.

    Product
    Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK, SOY. Distributed by Costco Wholesale Corp. PO Box 34535 Seattle, WA.
    Category
    Food
    Distribution
    24 states
  • HighFDA (Drugs)·D-0310-2026·2026-02-18

    Estradiol 15mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 14,848 pellets of ESTRADIOL, 15 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL,15 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3015-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0335-2026·2026-02-18

    Thiamine injection bags recalled over a lack of assurance of sterility

    Fresenius Kabi Compounding is recalling 10,548 bags of thiamine HCl 500 mg in sodium chloride injection over a lack of assurance of sterility.

    Product
    thiamine HCl, 500 mg, 500 mg added to 100 mL, 0.9% Sodium Chloride Injection, USP, Fagron Sterile Services, 20 Dan Road, Canton, MA 02021, NDC 71506-079-56.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1316-2026·2026-02-18

    IQon Spectral CT recalled over rotor fasteners that may be undertorqued

    Philips is recalling 52 IQon Spectral CT units because fasteners attaching the rotor to the gantry bearing may not be torqued to specification.

    Product
    IQon Spectral CT; Product Code (REF): 728332;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0307-2026·2026-02-18

    Estradiol 6mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 50,990 pellets of ESTRADIOL, 6 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 6 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3006-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0309-2026·2026-02-18

    Estradiol 12.5mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 22,478 pellets of ESTRADIOL, 12.5 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 12.5 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79599-3012-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1332-2026·2026-02-18

    Suture removal trays recalled over open swabstick applicator seals

    Medline is recalling 2,448 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: SUTURE REMOVAL TRAY, Kit SKU DYNDR1277A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1326-2026·2026-02-18

    Anesthesia artline packs recalled over open swabstick applicator seals

    Medline is recalling 120 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: ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0320-2026·2026-02-18

    Testosterone 50mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 70,959 pellets of Testosterone, 50.0 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 50.0 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1050-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0329-2026·2026-02-18

    Testosterone 200mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 7,840 pellets of Testosterone 200mg, Triamcinolone Acetonide 40mcg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone 200mg, Triamcinolone Acetonide 40mcg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-6200-43.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0324-2026·2026-02-18

    Testosterone 200mg single pellets recalled over potential metal particulate

    Asteria Health is recalling 194,336 pellets of Testosterone, 200 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone, 200 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-1200-43.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0327-2026·2026-02-18

    Testosterone 75mg and anastrozole pellets recalled over metal particulate matter

    Asteria Health is recalling 670 pellets of Testosterone 75mg, Anastrozole 4mg sterile pellets over the potential presence of metal particulate matter.

    Product
    Testosterone 75mg, Anastrozole 4mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-4079-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0312-2026·2026-02-18

    Estradiol 20mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 1,475 pellets of ESTRADIOL, 20 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 20 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3020-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0314-2026·2026-02-18

    Estradiol 25mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 2,442 pellets of ESTRADIOL, 25 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 25 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 35211, NDC: 79559-3025-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1328-2026·2026-02-18

    Pediatric catheter securement kits recalled over open swabstick seals

    Medline is recalling 450 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: PEDIATRIC CATH SECUREMENT DRSG, Kit SKU DYNDC3108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0311-2026·2026-02-18

    Estradiol 18mg pellets recalled over potential metal particulate matter

    Asteria Health is recalling 1,699 pellets of ESTRADIOL, 18 mg sterile pellets over the potential presence of metal particulate matter.

    Product
    ESTRADIOL, 18 mg, 1 Sterile Pellet, Asteria Health 432 Industrial Ln, Birmingham, AL 3521, NDC: 79559-3018-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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 (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-1340-2026·2026-02-18

    GammaPlan software recalled over plans that may irradiate the wrong location

    Elekta is recalling Leksell GammaPlan versions 11.3 and 11.4 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: 11,3, 11.4 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-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-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-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