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.

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.

2926–2950 of 78628

  • SevereFDA (Drugs)·D-0396-2026·2026-03-11

    Mojo Max Fusion capsules recalled as Class I over undeclared drug ingredients

    Mojo Max Fusion XXX capsules are being recalled because FDA analysis revealed undeclared sildenafil at 13.1 mg per capsule and tadalafil at 13.8 mg per capsule. The FDA has classified this recall as Class I.

    Product
    Mojo Max Fusion XXX, 500 mg, one capsule per blister card, 20 count box, Distributed by: Max Nutrition Inc. UPC 6 78945 36675 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1471-2026·2026-03-11

    Abiomed Impella RP recalled as Class I over sensor malfunction risk

    Abiomed is recalling the Impella RP, product code 0046-0011, because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.

    Product
    Impella RP. Product Code: 0046-0011.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1482-2026·2026-03-11

    B. Braun 21GA winged infusion single packs may have blunt needles

    B. Braun Medical is recalling 21GA Winged Infusion single packs, model 7A3842, because the needle tip may be dull or blunt, difficult to advance, or may break.

    Product
    Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneou
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1483-2026·2026-03-11

    B. Braun 21GA winged infusion sets may have blunt needle tips

    B. Braun Medical is recalling 21GA Winged Infusion Sets, model 7M2802, because the needle tip may be dull or blunt, difficult to advance, or may break.

    Product
    Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1476-2026·2026-03-11

    Roche cobas analyzer may repeat previous results for spline calibrated assays

    Roche is recalling cobas pro sample supply units on software versions before 03-02 because a defect can make the analyzer repeat the last calculated result for all later measurements.

    Product
    cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample supply unit, material number 08464502001 cobas pro SSU, material number 09205632001 Affected Assays: (Product Name/ Catalog Number/ Application Code/ Application Short Name) 1. Cystati
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1479-2026·2026-03-11

    Olympus lithotripsy generator recalled over transducer recognition failure

    Olympus is recalling the ShockPulse-SE Lithotripsy System Generator after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.

    Product
    Brand Name: ShockPulse-SE Lithotripsy System Product Name: ShockPulse-SE Lithotripsy System - Generator Model/Catalog Number: SPL-G Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0354-2026·2026-03-11

    Teva metoprolol succinate 25 mg tablets failed dissolution specifications

    Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 25 mg after the product failed dissolution specifications.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1481-2026·2026-03-11

    B. Braun 21G 4.4 cm winged infusion needles may break

    B. Braun Medical is recalling 21G x 4.4 cm Winged Infusion devices, model 7B3050, because the needle tip may be dull or blunt, difficult to advance, or may break.

    Product
    Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percut
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1490-2026·2026-03-11

    Esaote endocavity ultrasound probe recalled because liquid may leak in

    Esaote is recalling five Endocavity ultrasonic probes, model E 3-12, because a potential weakness in the probe body may allow liquid to leak from the casing near the cable.

    Product
    Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0355-2026·2026-03-11

    Teva metoprolol succinate 50 mg tablets failed dissolution specifications

    Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 50 mg after the product failed dissolution specifications.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0389-2026·2026-03-11

    Sodium iodide I-131 oral solution recalled over particulate matter

    Radnostix is recalling one batch of Sodium Iodide I-131 Therapeutic Oral Solution because of the presence of particulate matter caused by production issues.

    Product
    SODIUM IODIDE I-131 — SODIUM IODIDE I-131 (SODIUM IODIDE I-131)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V136000·2026-03-11

    Volvo EX30 seat belt warning chime may not sound as intended

    Volvo is recalling certain 2025-2026 EX30 and 2026 EX30CC vehicles because the seat belt warning system may not activate the audible warning chime. This fails FMVSS 208.

    Product
    VOLVO — VOLVO EX30CC, EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1477-2026·2026-03-11

    Olympus lithotripsy reusable probes recalled over generator transducer recognition failure

    Olympus is recalling ShockPulse-SE Lithotripsy System reusable probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.

    Product
    Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1485-2026·2026-03-11

    Aesculap MINOP trocar shafts may be longer than specified

    Aesculap is recalling MINOP Trocar 150 mm with 6.0 mm working channel, model FF399R, because of the potential for the trocar shaft to be too long.

    Product
    Brand Name: AESCULAP Product Name: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Model/Catalog Number: FF399R Software Version: N/A Product Description: MINOP TROCAR 150MM 4 WKING CHANNEL6.0MM Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1484-2026·2026-03-11

    Siemens urine albumin assay may report falsely depressed patient results

    Siemens Healthcare Diagnostics is recalling all lots of the Atellica CH Urine Albumin assay because falsely depressed patient results may occur above the measuring interval.

    Product
    Atellica CH Urine Albumin (UAlb). Material Number: 11537225
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1489-2026·2026-03-11

    Olympus biopsy valve MAJ-1218 may shed rubber fragments during use

    Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-1218, because of the potential for rubber fragment detachment during use.

    Product
    Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent leakage of body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1478-2026·2026-03-11

    Olympus lithotripsy single use probes recalled over generator recognition failure

    Olympus is recalling ShockPulse-SE Lithotripsy System single use probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.

    Product
    Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V137000·2026-03-11

    ARBOC Transit Buses Recalled for Rear Brake Line Installation Error

    ARBOC is recalling 2018-2026 Spirit of Freedom and Spirit of Mobility buses because incorrectly installed rear brake lines may cause the anti-lock brake system to malfunction.

    Product
    ARBOC SPECIALTY VEHICLES — ARBOC SPECIALTY VEHICLES SPIRIT OF FREEDOM, SPIRIT OF MOBILITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1475-2026·2026-03-11

    GE radiology viewer may show patient information not matching displayed images

    GE Healthcare is recalling Centricity Universal Viewer Zero Footprint Client because under certain workflows the patient information shown may not match the images displayed.

    Product
    GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: 2110344-039, 2110344-046, 2110344-047; System, Image Processing, Radiological
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0357-2026·2026-03-11

    Teva metoprolol succinate 200 mg tablets failed dissolution specifications

    Teva Pharmaceuticals is recalling three lots of Metoprolol Succinate Extended-Release Tablets 200 mg after the product failed dissolution specifications.

    Product
    METOPROLOL SUCCINATE — METOPROLOL SUCCINATE (METOPROLOL SUCCINATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V138000·2026-03-11

    2025–2026 Volkswagen Jetta Vehicles Recalled for Transmission Ground Wire

    Volkswagen is recalling certain 2025–2026 Jetta vehicles because the transmission ground wire may not have been properly connected during assembly, creating an open electrical circuit that could increase fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1488-2026·2026-03-11

    Olympus single use biopsy valve may shed rubber fragments during use

    Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-210, because of the potential for rubber fragment detachment during use.

    Product
    Olympus Single use Biopsy Valve. Model/Catalog Number: MAJ-210. 20 units per box. The MAJ-210 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent reflux of body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide