The Recall Desk

State

Nevada product recalls

73,363 recalls have nationwide distribution and so reach Nevada. 5,696 additional recalls listed Nevada specifically in their distribution scope.

What the numbers show

Total
5,696
Critical
951
Severe
1,479
Most recent
2026-09-25

Of the 5,696 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 1,479 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,696 recalls whose distribution notice names Nevada specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

17301–17325 of 79059

  • HighFDA (Devices)·Z-1562-2023·2023-05-10

    Laboratory Automation Module Firmware May Cause Sample Misidentification

    Vesmatic Cube 80 laboratory automation system firmware can incorrectly identify patient samples, potentially leading to wrong test results and inappropriate treatment. Affected systems include FlexLab, Accelerator a3600, and Aptio Automation units.

    Product
    Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand names of the same product: FlexLab (FLX), Accelerator a3600 (ACP), Aptio Automation (AP2) Part Numbers: 72747000.A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1508-2023·2023-05-10

    Linkbio LINK SLED Knee implant system recalled for surgical technique requirements

    Linkbio Corp. recalls LINK SLED Knee System implants due to risk of early loosening and increased wear caused by improper surgical technique. Updated training and labeling have been issued.

    Product
    LINK SLED Knee System: ENDO SLED KNEE FEM COMP, MEDIUM SMALL Item Number: 15-2020/46
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1523-2023·2023-05-10

    LINK SLED Knee System tibial component recall due to implant positioning and cementing concerns

    Linkbio Corp. is recalling LINK SLED Knee System tibial components due to risk of early loosening or increased wear caused by suboptimal implant positioning or inadequate cementing technique. Surgeons are being directed to update their technique and receive additional training.

    Product
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 7MM X 58MM Item Number: 15-2028/13
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0798-2023·2023-05-10

    Cargill Soy Flour Recalled for Possible Gluten Contamination

    Cargill is recalling PROSANTE soy flour products labeled gluten-free because they may contain gluten levels above 20 ppm, the FDA's regulatory threshold for gluten-free labeling. Products were distributed nationwide and internationally.

    Product
    PROSANTE TSOYFLR 7P MNCD 25LB BG/40P, PROSANTE TSOYFLR 7P MNCD 50LB BG, 25 lb and 50lb paper bags
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1518-2023·2023-05-10

    LINK SLED Knee Implant Component Recalled Due to Early Loosening Risk

    FDA recalls LINK SLED Knee System tibial components due to risk of aseptic loosening and premature wear. Patients may require revision surgery.

    Product
    LINK SLED Knee System: ALL POLY TIBIAL COMPONENT 13MM X 50MM Item Number: 15-2028/08
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0786-2023·2023-05-10

    Prosante TVGPTN Food Products Recalled for Potential Gluten Contamination

    Cargill is recalling Prosante TVGPTN food products labeled as gluten-free that may contain gluten above 20 ppm.

    Product
    PROSANTE TVGPTN 10BF MNCD 25LB BG/40P, PROSANTE TVGPTN 10BF MNCD 50LB BG/36P, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0784-2023·2023-05-10

    Gluten-Free Labeled Poultry Ingredient May Contain Undisclosed Gluten

    Cargill is recalling PROSANTE TVGPTN 3018B FLK poultry ingredient because products labeled gluten-free may contain gluten levels above 20 ppm, the legal threshold for gluten-free claims.

    Product
    PROSANTE TVGPTN 3018B FLK 50LB BG, paper bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2023·2023-05-10

    Knee implant system recall due to aseptic loosening from improper surgical technique

    Linkbio Corp. recalls LINK SLED Knee System tibial component due to risk of early aseptic loosening caused by inadequate surgical technique. Training on improved surgical technique is being provided.

    Product
    LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 9 MM X 50 MM Item Number: 15-2230/06
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0559-2023·2023-05-10

    Drug Recall: Glimepiride 4 mg for Manufacturing Practice Deviations

    PD-Rx Pharmaceuticals is recalling 186 bottles of Glimepiride USP 4 mg due to manufacturing deviations. Patients using this medication should contact their healthcare provider to verify if their supply is affected.

    Product
    Glimepiride USP, 4 mg, 90 count-bottles, Rx only, Intas Pharm. Limited Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127, NDC 43063-0587-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0557-2023·2023-05-10

    Drug Recall: Montelukast Sodium Tablets Due to Manufacturing Deviations

    PD-Rx Pharmaceuticals has recalled 352 bottles of Montelukast Sodium USP 10 mg tablets distributed nationwide due to manufacturing process deviations. This was a voluntary recall by the firm.

    Product
    Montelukast Sodium USP, 10 mg, 30 count-bottles, Rx only, Intas Pharm, Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127, NDC 43063-0762-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0563-2023·2023-05-10

    Advil Ibuprofen Tablets Recalled for Storage Temperature Deviation

    Family Dollar Stores is recalling Advil Ibuprofen 200 mg tablets due to a storage temperature deviation during manufacturing and distribution. No illnesses have been reported.

    Product
    Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1556-2023·2023-05-10

    VITROS 5600 system pack opener assembly may not function properly

    The MicroTip Pack Opener Assembly on VITROS 5600 systems may fail to remove or replace pack caps properly, making packs unusable and delaying clinical test results. Approximately 4,895 units were distributed.

    Product
    VITROS 5600 Integrated System- For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products MicroSlides, VITROS Chemistry Products MicroTip Reagents and VITROS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1557-2023·2023-05-10

    VITROS 5600 Integrated System MicroTip Pack Opener Assembly Defect

    Refurbished VITROS 5600 diagnostic systems may have a defective MicroTip Pack Opener Assembly that fails to properly remove or replace pack caps, potentially causing delayed test results. Ortho-Clinical Diagnostics is recalling 1,148 units distributed nationwide and internationally.

    Product
    VITROS 5600 Integrated System - Refurbished . For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products MicroSlides, VITROS Chemistry Products MicroTip Reagents and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0808-2023·2023-05-10

    Atkins Milk Chocolate Delight Protein Shakes Recalled for Spoilage Risk

    Simply Good Foods is recalling Atkins Milk Chocolate Delight Protein Shakes nationwide due to post-processing contamination that may cause spoilage. Affected products have lot numbers SA2208P3F6 (exp. 07/27/23) or SA2210P3F6 (exp. 07/29/23).

    Product
    Atkins Milk Chocolate Delight Protein Rich Shakes, NET WT. 44 oz (4 / 11oz), 4 Tetra Packs per carton, UPC 637480065016, Distributed exclusively by Simply Good Foods USA, Inc. Denver, CO 80202, 1-800-6-ATKINS
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0565-2023·2023-05-10

    Advil Dual Action Pain Reliever Recalled for Storage Temperature Deviation

    Family Dollar Stores is recalling Advil Dual Action pain reliever tablets (36-caplet bottles, SKU 0902867) nationwide because the product was stored outside labeled temperature requirements.

    Product
    Advil Dual Action with Acetaminophen Acetaminophen 250 mg and Ibuprofen (NSAID) 125 mg Tablets Pain Reliever, 36 Caplets bottles
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1555-2023·2023-05-10

    VITROS XT 7600 Analyzer Pack Opener May Not Remove Reagent Pack Caps

    The MicroTip Pack Opener Assembly in VITROS XT 7600 laboratory analyzers may fail to properly remove or replace reagent pack caps, potentially causing unusable packs and delayed test results. Approximately 2,001 affected units were distributed nationwide and internationally.

    Product
    VITROS XT 7600 Integrated System - For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Chemistry Products MicroSlides, VITROS Chemistry Products MicroTip Reagents and VITROS…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1482-2023·2023-05-10

    Hill-Rom Pro+ Hospital Mattress Covers Recalled for Delamination Risk

    Baxter is recalling Hill-Rom pro+ mattress covers that may delaminate, allowing fluid to seep into the mattress. No injuries have been reported.

    Product
    Hill-Rom pro+ mattress, product codes (REF): a) 20877002S, b) 20877003S, c) 20877004S, d) 20877007S, e) 20877008S, f) 21649301S, g) 21649401S, h) 21649402S, i) P006800A01, j) P006800A02, k) P3255A01, l) P3255A02, m) P3255A03, n) P3255ARENT01, o) P7923A01, p) P7923A02, q)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1506-2023·2023-05-10

    DERMLITE DL4W Medical Device Recalled for Serial Number Labeling Discrepancy

    DermLite LLC is recalling DERMLITE DL4W diagnostic devices due to incorrect package labeling. The serial number on the package differs from the serial number on the product itself.

    Product
    DERMLITE DL4W, REF: DL4W, Rx Only MD, CE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0814-2023·2023-05-10

    Nuts & Grain Bread Recalled for Undeclared Tree Nut Cross Contamination

    Signature Select Nuts & Grain Bread may contain undeclared tree nuts from potential cross contamination. The product is distributed in Western U.S. states and poses a risk to consumers with tree nut allergies.

    Product
    Signature Select Nuts & Grain Bread NET WT 20 OZ (1 LB 8 OZ) 680 g Ingredients: Unbleached enriched wheat flour (wheat flour, malted barley flour, reduced iron, niacin, thiamine, mononitrate, riboflavin, folic acid), water, walnuts, whole grain bulgur wheat, whole grain oats…
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Drugs)·D-0556-2023·2023-05-10

    Lidocaine Patch 5% Recalled for Typographical Error on Label

    Bryant Ranch Prepack is recalling Lidocaine Patch 5% nationwide due to a typographical error on product labels. The labels incorrectly state 'tablet' instead of 'patch', creating potential confusion about the dosage form.

    Product
    LIDOCAINE — LIDOCAINE (LIDOCAINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0813-2023·2023-05-10

    Signature Select Oat & Nuts Bread Recalled for Potential Tree Nut Cross-Contamination

    Albertsons Companies LLC is recalling Signature Select Oat & Nuts Bread (20 oz) due to potential undeclared tree nut allergens from cross-contamination. Consumers with tree nut allergies should not consume affected products.

    Product
    Signature Select Oat & Nuts Bread NET WT 20 OZ (1 LB 8 OZ) 680 g Ingredients: Unbleached enriched wheat flour (wheat flour, malted barley flour, reduced iron, niacin, thiamine, mononitrate, riboflavin, folic acid), water, whole grain, oats, liquid sugar, yeast, hazelnuts…
    Category
    Food
    Distribution
    6 states
  • ModerateFDA (Devices)·Z-1545-2023·2023-05-10

    LINK SLED Knee Implant Surgical Technique Update Required

    The LINK SLED Knee System requires updated surgical technique training due to risks of aseptic loosening and implant wear when improperly positioned or cemented. The manufacturer is issuing reinforced surgical guidelines and training to prevent unsatisfactory outcomes.

    Product
    LINK SLED Knee System POREX ENDO MODEL SLED TIBIAL COMP 13 MM X 45 MM Item Number: 15-2230/04
    Category
    Medical Device
    Distribution
    2 states
  • ModerateFDA (Drugs)·D-0558-2023·2023-05-10

    Simvastatin USP Tablets Recalled Due to Manufacturing Quality Deviations

    PD-Rx Pharmaceuticals is recalling Simvastatin USP 10 mg tablets due to manufacturing quality deviations. The recall affects 37 bottles distributed nationwide.

    Product
    Simvastatin USP, 10 mg, Rx only, Intas Pharm, Limited Ahmedabad 380 054 India Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 30 count-bottle (NDC 43063-0727-30) b) 90 count-bottle (NDC 43063-0727-90)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1558-2023·2023-05-10

    DeVilbiss Healthcare 1025 Series Oxygen Concentrator Instruction Manual Update

    DeVilbiss Healthcare is updating the instruction manual for its 1025 Series Oxygen Concentrator to comply with IEC-60101-1 standard labeling requirements. This recall affects 143,397 units distributed nationwide and worldwide.

    Product
    DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR, Model Numbers 1025DS, 1025UK, 1025KS, and 1025KS-AR
    Category
    Medical Device
    Distribution
    Distributed nationwide