The Recall Desk

State

Nevada product recalls

72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3501–3525 of 78632

  • HighFDA (Food)·H-0429-2026·2026-02-04

    Dairy free roasted green chile tamales recalled over potential Listeria

    Prima Vera Nueva is recalling 21,705 packages (4 tamales per package) of Roasted Green Chile Tamales over potential contamination with Listeria monocytogenes.

    Product
    Roasted Green Chile Tamales NO DAIRY Ingredients: Organic Corn Flour Masa, Roasted Green Chiles, Non-GMO Corn, Non-hydrogenated Vegetable Shortening, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and Monocalcium Phosphate), Water, Citric
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1171-2026·2026-02-04

    Push-in suture anchors recalled after reports of breakage and pull out

    Aju Pharm is recalling 200 units of the Genesis Push-In Suture Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Genesis Push-In Suture Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1206-2026·2026-02-04

    Ingenia 1.5T systems recalled over elastography stiffness value errors

    Philips North America is recalling 10 units of the Ingenia 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia 1.5T. Product Code (REF): (1) 781341, (2) 781396. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1216-2026·2026-02-04

    SmartPath dStream upgrades recalled over elastography stiffness value errors

    Philips North America is recalling 3 units of the SmartPath to dStream for XR and 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    SmartPath to dStream for XR and 3.0T. Product Code (REF): 781270. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0427-2026·2026-02-04

    BBQ chipotle bean tamales recalled over potential Listeria contamination

    Prima Vera Nueva is recalling 27,964 packages (4 tamales per package) of BBQ Chipotle Bean & White Cheddar Tamales over potential contamination with Listeria monocytogenes.

    Product
    BBQ Chipotle Bean & White Cheddar Tamales Ingredients: Organic Corn Flour Masa, Beans, Jack Cheese (Pasteurized Milk, Cheese Cultures, Salt and Enzymes), Salsa (Tomatoes, Onions, Chiles, Garlic & Cilantro), Butter, Non-GMO Corn, Salt, Spices, Baking Powder (Sodium Acid Pyrophosp
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1208-2026·2026-02-04

    Ingenia 3.0T CX systems recalled over elastography stiffness value errors

    Philips North America is recalling 6 units of the Ingenia 3.0T CX MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1207-2026·2026-02-04

    Dual thread screw-in anchors recalled after reports of device failure

    Aju Pharm is recalling 400 units of the Genesis Dual Thread Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Ingenia 3.0T. Product Code (REF): (1) 781342, (2) 781377. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1183-2026·2026-02-04

    Toothbrushes recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling toothbrushes and toothpaste-with-brush packs over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Toothbrushes, labeled as: ORAL B TOOTH BRUSH SHINY CLEAN SOFT 12CT; COLGATE TOOTH BRUSH MED. 12CT; ADULT TOOTHPASTE W BRUSH (WHITENING) 6.4oz/24ct; ADULT TOOTHPASTE W BRUSH (ANTICAV) 6.4oz/24ct.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0432-2026·2026-02-04

    Green chile and jack cheese tamales recalled over potential Listeria

    Prima Vera Nueva is recalling 31,672 packages (4 tamales per package) of Roasted Green Chile & Jack Cheese Tamales over potential contamination with Listeria monocytogenes.

    Product
    Roasted Green Chile & Jack Cheese Tamales Ingredients: Organic Corn Flour Masa, Roasted Green Chiles, Jack Cheese (Pasteurized Milk, Cheese Cultures, Salt, Enzymes), Non-GMO Corn, Butter, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Corn Starch and
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1210-2026·2026-02-04

    Ingenia Ambition X systems recalled over elastography stiffness value errors

    Philips North America is recalling 21 units of the Ingenia Ambition X because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Ingenia Ambition X. Product Code (REF): (1) 781356, (2) 782109, (3)782138. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1219-2026·2026-02-04

    Central line dressing kits recalled over open swabstick applicator seals

    LSL Healthcare is recalling 1,400 Central Line Dressing Kits because the BD ChloraPrep Triple Swabsticks inside exhibit an open seal on the applicator packaging.

    Product
    LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2519CP, medical procedure convenience kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1204-2026·2026-02-04

    Evolution Upgrade 1.5T systems recalled over elastography stiffness value errors

    Philips North America is recalling 3 units of the Evolution Upgrade 1.5T MR system because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    Evolution Upgrade 1.5T. Product Codes (REF): (1) 782148, (2) 782116. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1203-2026·2026-02-04

    Chest drainage units recalled to limit their use to adults

    Cardinal Health is updating the instructions for use on 1,169,726 chest drainage units to clarify that the intended patient population is adults 18 years and older.

    Product
    Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health Sentinel Seal CDU 2. 8888571513 Cardinal Health Sentinel Seal CDU, Dual Drain 3. 8888571489 Cardinal Health Sentinel Seal CDU, with Easy Change Connector 4. 8888571370 Cardinal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0430-2026·2026-02-04

    Dairy free butternut squash tamales recalled over potential Listeria contamination

    Prima Vera Nueva is recalling 18,876 packages (4 tamales per package) of Butternut Squash Tamales with Roasted Green Chiles over potential contamination with Listeria monocytogenes.

    Product
    Butternut Squash Tamales with Roasted Green Chiles, NO DAIRY Ingredients: Organic Corn Flour Masa, Organic Butternut Squash, Roasted Green Chiles, Non-GMO Corn, Non-hydrogenated Vegetable Shortening, Salt, Spices, Baking Powder (Sodium Acid Pyrophosphate, Sodium Bicarbonate, Cor
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1215-2026·2026-02-04

    SmartPath dStream 3.0T upgrades recalled over elastography stiffness errors

    Philips North America is recalling 1 unit of the SmartPath to dStream for 3.0T because exported MR Elastography stiffness maps may show stiffness value errors.

    Product
    SmartPath to dStream for 3.0T. Product Code (REF): 782145. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1174-2026·2026-02-04

    Roasted pumpkin tamales recalled over potential Listeria monocytogenes contamination

    Prima Vera Nueva is recalling 9,656 packages (4 tamales per package) of Roasted Pumpkin & White Cheddar Tamales over potential contamination with Listeria monocytogenes.

    Product
    Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix R; Siemens Material Number (SMN): 11574002; With Software Version VB10D-SP02
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2026·2026-02-04

    Condoms recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1185-2026·2026-02-04

    Conductivity standard solutions recalled over incorrect dialysate conductivity values

    NIPRO Technical Services is recalling 499 units of Conductivity Standard Solution because a defect in the solution can cause meters to report incorrect conductivity values for dialysate.

    Product
    Conductivity Standard Solution Catalog/Model Numbers: 10001, 10011, 10021, 10032, 10040, 10040c, and 10041 Conductivity Standard Solutions are a secondary standard solution used for the calibration of conductivity cells together with conductivity meters
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1179-2026·2026-02-04

    Q.namix R fluoroscopy systems recalled over unflipped and mismatched images

    Siemens is recalling 41 units of the LUMINOS Q.namix R fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.

    Product
    Alphenix INFX-8000V, interventional fluoroscopic x-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1175-2026·2026-02-04

    Q.namix T fluoroscopy systems recalled over unflipped and mismatched images

    Siemens is recalling 7 units of the LUMINOS Q.namix T fluoroscopic X-ray system because ortho images may not be flipped as preset and an image of a previous patient may be processed.

    Product
    Interventional Fluoroscopic X-Ray System: LUMINOS Q.namix T; Siemens Material Number (SMN): 11574003; With Software Version VB10D-SP02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0426-2026·2026-02-04

    Mushroom and spinach tamales recalled over potential Listeria contamination

    Prima Vera Nueva is recalling 16,264 packages (4 tamales per package) of Mushroom over potential contamination with Listeria monocytogenes.

    Product
    Mushroom, Spinach & Salsa Tamales No Dairy Ingredients: Organic Corn Flour Masa, Mushrooms, Spinach, Tomatoes, Onions, Jalapenos, Non-hydrogenated Vegetable Shortning, Salt, Spices, Baking Powder. Microwave: In husk approx. 90 seconds per tamale. Steam: In husk approx. 15 minut
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1173-2026·2026-02-04

    AlternatiV+ screw-in anchors recalled after reports of device failure

    Aju Pharm is recalling 416 units of the AlternatiV+ Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    AlternatiV+ Screw-In Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1167-2026·2026-02-04

    Biocomposite suture anchors recalled after reports of breakage and bending

    Aju Pharm is recalling 1,088 units of the Fixone Biocomposite Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Fixone Biocomposite Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide