The Recall Desk

State

Nevada product recalls

72,919 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 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2676–2700 of 78611

  • HighFDA (Devices)·Z-1610-2026·2026-04-01

    Olympus endoscope suction valve no longer compatible with named reprocessors

    Olympus is recalling the MAJ-1443 Endoscope Suction Valve because the MAJ-1443 and MAJ-1444 are no longer reprocessing compatible with the OER-Pro and OER-Elite automated endoscope reprocessors.

    Product
    Olympus Endoscope Suction Valve - MAJ-1443. Model Number: MAJ-1443.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0592-2026·2026-04-01

    Trader Joe's Vegetable Fried Rice recalled for glass fragments

    Ajinomoto Foods North America Inc. is recalling Trader Joe's Vegetable Fried Rice (1 lb bags, Item 5650233) due to glass fragments (1–3 cm long, 2–4 mm wide) found in the product. The recall affects approximately 9.9 million pounds distributed across 40 US states.

    Product
    Item 5650233 Trader Joe's Vegetable Fried Rice, net wt. 1lb per bag. Retail bag UPC 00521482. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 24/1lb. bags per case. Case UPC 10052148200001. All products are intended t
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·H-0600-2026·2026-04-01

    Ajinomoto Vegetable Gyoza Dumplings recalled for glass fragments

    Ajinomoto Foods North America Inc. is recalling Vegetable Gyoza Dumplings (UPC 071757055483) due to the presence of glass fragments in the product, which could pose a choking or injury hazard if ingested.

    Product
    Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct. Net wt. 8.92oz. per package. Retail package UPC: 071757055483. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 20/8.92oz. packages or 11.15 lbs. per case. Carton UP
    Category
    Food
    Distribution
    43 states
  • HighFDA (Devices)·Z-1640-2026·2026-04-01

    Olympus PK cutting forceps jaws may break from defective welds

    Olympus is recalling PK Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.

    Product
    Brand Name: Olympus PK Cutting Forceps, 5mm 33cm Product Name: PK Cutting Forceps Model/Catalog Number: PK-CF0533 Product Description: An assembly of devices intended to generate and apply radio-frequency (RF) alternating current to soft tissues for cutting and coagulation dur
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1639-2026·2026-04-01

    Olympus Everest bipolar cutting forceps jaws may break from defective welds

    Olympus is recalling Everest Bipolar Cutting Forceps because a supplier did not adequately validate the welding process, and defective welds can cause the forceps jaw to break during clinical use.

    Product
    Brand Name: Olympus Everest Bipolar Cutting Forceps w/Cord, 5mm 33 cm Product Name: Everest Bipolar Cutting Forceps Model/Catalog Number: 3006 Product Description: The OLYMPUS Everest Bipolar Cutting Forceps are intended to be passed through a 5 mm cannula. Coagulation is achi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1633-2026·2026-04-01

    Straumann angled custom abutments made from wrong bar material

    Straumann is recalling Custom Abutment AS Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.

    Product
    Custom Abutment AS Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 010.5438;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0590-2026·2026-04-01

    Chilli Spanish Peanuts Recalled for Glass Contamination Risk

    Western Mixers Produce & Nuts, Inc. is recalling Treasured Harvest brand Chilli Spanish Peanuts (25lb bags, Lot #260230) due to glass fragments found in sealed containers.

    Product
    Chilli Spanish Peanuts, Treasured Harvest brand, 25lb clear plastic bag container. UPC:none Item code: 2608-25
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0597-2026·2026-04-01

    Ajinomoto Tai Pei Shrimp Fried Rice Recalled for Glass Contamination

    Ajinomoto Foods North America Inc. is recalling Tai Pei Shrimp Fried Rice due to glass fragments found in the product. Glass pieces measuring 1–3 cm long and 2–4 mm wide pose a choking and injury risk.

    Product
    Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp, vegetables & fried rice with oyster flavored sauce. Net wt. 48oz or 3lbs. per box. Retail box UPC 070077811465. Product packaging is flexible bags in a master case or flexible bags in cartons in a master case. There are 4
    Category
    Food
    Distribution
    43 states
  • HighFDA (Food)·H-0596-2026·2026-04-01

    Ajinomoto Ling Ling Fried Rice Recalled for Glass Contamination

    Ajinomoto Foods North America is recalling Item 81097 Ling Ling Restaurant Style Fried Rice due to glass fragments measuring 1-3 cm long and 2-4 mm wide found in the product. Affected units with Best By dates 9/21/2026 through 3/8/2027 were distributed across 40 U.S. states.

    Product
    Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory Vegetable - A Chinese Style Fried Rice with Edamame, Carrots, Fire Roasted Corn & Red Bell Peppers Prepared with Sweet Soy Sauce Infused Rice. Net wt. 17oz. Retail box UPC 010878810915. Product packaging is flexib
    Category
    Food
    Distribution
    43 states
  • HighFDA (Devices)·Z-1601-2026·2026-04-01

    I.T.S. fibula and tubular plates heat more in MRI than stated

    I.T.S. GmbH is recalling the Fibula Plate PROlock with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    I.T.S. Fibula Plate PROlock with Angular Stability with the below descriptions and corresponding article numbers. 1. Distal Tubular Plate; Article Numbers: 21602-3, 21602-4, 21602-5, 21602-6, 21602-7, 21602-8, 21603-3, 21603-4, 21603-5, 21603-6, 21603-7, 21603-8. 2. Fibul
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1632-2026·2026-04-01

    Straumann custom abutments made from wrong bar material after mix-up

    Straumann is recalling Custom Abutment Ti for Straumann RC because a material mix-up meant titanium abutments were manufactured from TAN bar material instead of Titanium Grade 4.

    Product
    Custom Abutment Ti, for Straumann RC, incl. TAN screw; Catalog Number/Art.: 027.4620;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1595-2026·2026-04-01

    I.T.S. calcaneus repair plate heats more in MRI than stated

    I.T.S. GmbH is recalling the FR.O.H. Calcaneus Repair System anterolateral calcaneus plate because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use reflected.

    Product
    FR.O.H. Calcaneus Repair System with the following description: Anterolateral Calcaneus Plate. Article Number: 21064-60.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1613-2026·2026-04-01

    Olympus OER-Pro reprocessor no longer compatible with two valve models

    Olympus is recalling the OER-Pro Endoscope Reprocessor because the MAJ-1443 and MAJ-1444 air/water valves are no longer reprocessing compatible with the OER-Pro and OER-Elite reprocessors.

    Product
    Olympus Endoscope Reprocessor OER-Pro. Model Number: N3058140.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1602-2026·2026-04-01

    I.T.S. distal humeral plates heat more in MRI than stated

    I.T.S. GmbH is recalling Distal Humeral Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    Distal Humeral Plates with Angular Stability with the below descriptions and corresponding article numbers. 1. Cortical Screw, Locking; Article Numbers: 37351-10-N, 37351-12-N, 37351-14-N, 37351-16-N, 37351-18-N, 37351-20-N, 37351-22-N, 37351-24-N, 37351-26-N, 37351-28-N, 373
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1593-2026·2026-04-01

    I.T.S. clavicle plates heat more in MRI than instructions state

    I.T.S. GmbH is recalling Clavicula Plates with Angular Stability because updated MRI safety testing shows higher RF-induced temperature increases than the Instructions for Use previously reflected.

    Product
    Claviculaplate with Angular Stability, with the below descriptions and associated article numbers. 1. Anterior Clavicle Plate, Medial; Article Numbers: 21116-8, 21117-10, 21118-10. 2. Clavicle Plate; Article Numbers: 21121-6, 21121-8. 3. Clavicle Plate, 3.5mm; Article
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1650-2026·2026-04-01

    Puracol collagen wound dressings recalled over elevated endotoxin levels

    Medline is recalling Puracol and Puracol Plus collagen wound dressings after elevated endotoxin levels were identified in affected lots.

    Product
    Puracol and Puracol Plus Collagen Wound Dressings: MSC8522 DRESSING,COLLAGEN,PURACOL,STRL,2" X 2" MSC8622EP DRESSING,COLLAGEN,PURACOL PLUS, 2X2.2"
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0401-2026·2026-04-01

    Sodium iodide capsule packs recalled after failing capsule specifications

    Radnostix is recalling three lots of the Gelatin Capsule Pack used with the Sodium Iodide I-131 Kit because the product failed tablet and capsule specifications.

    Product
    SODIUM IODIDE I-131 — SODIUM IODIDE I-131 (SODIUM IODIDE I-131)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0624-2026·2026-04-01

    Tops GOLD Mixed Pickle Recalled for Potential Erucic Acid Adulteration

    Mangalm LLC is recalling Tops GOLD Mixed Pickle due to potential adulteration with erucic acid from the mustard oil ingredient. The affected products were distributed in CA, NV, OR, UT, and WA.

    Product
    Tops GOLD Mixed Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288611380 INGREDIENTS:***Mustard Oil*** Tops GOLD Mixed Pickle NET QTY.: 158.73oz PRODUCT OF INDIA UPC: 8904288612950 INGREDIENTS:***Mustard Oil***
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Food)·H-0625-2026·2026-04-01

    Tops GOLD Mango Pickle recalled for potential erucic acid adulteration

    Mangalm LLC is recalling Tops GOLD Mango Pickle because the mustard oil ingredient may contain erucic acid, a potentially harmful compound. The affected products were distributed in California, Nevada, Oregon, Utah, and Washington.

    Product
    Tops GOLD Mango Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288611373 INGREDIENTS:***Mustard Oil*** Tops GOLD Mango Pickle NET QTY.: 158.73oz PRODUCT OF INDIA UPC: 8904288611915; 8904288613025 INGREDIENTS:***Mustard Oil***
    Category
    Food
    Distribution
    5 states
  • ModerateFDA (Devices)·Z-1645-2026·2026-04-01

    BD Alaris system labeling omits required TLS version for secure Wi-Fi

    CareFusion is recalling the BD Alaris System with Guardrails Suite MX because the product labeling does not indicate which TLS version must be enabled on the hospital network for secure Wi-Fi communication.

    Product
    BD Alaris" System with Guardrails" Suite MX with Point of Care Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1631-2026·2026-04-01

    BiDop 3 pocket Doppler labeling includes uncleared fetal indication

    Koven Technology is recalling the BiDop 3 Pocket Doppler packaged with a fetal probe because the product labeling includes a fetal indication for use that is not cleared under its 510(k).

    Product
    Brand Name: BiDop 3 Product Name: BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe Model/Catalog Number: ES-100V3 (device); BT2M20S8C (2 MHz fetal probe). Software Version: N/A Product Description: Hand-held, battery-powered ultrasonic Doppler blood-flow detector
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0628-2026·2026-04-01

    Tops GOLD Stuffed Red Chilli Pickle recalled for potential erucic acid contamination

    Mangalm LLC is recalling Tops GOLD Stuffed Red Chilli Pickle due to potential adulteration with erucic acid from mustard oil. The affected product was distributed in CA, NV, OR, UT, and WA.

    Product
    Tops GOLD Stuffed Red Chilli Pickle NET QTY.: 31.74oz PRODUCT OF INDIA UPC: 8904288611953 INGREDIENTS:***Mustard Oil***
    Category
    Food
    Distribution
    5 states
  • LowFDA (Devices)·Z-1627-2026·2026-04-01

    Philips X3-1 ultrasound transducer labelling updated to define useful life

    Philips is recalling the X3-1 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips X3-1 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1620-2026·2026-04-01

    Philips L12-5 ultrasound transducer labelling updated to define useful life

    Philips is recalling the L12-5 Ultrasound Transducer to provide clarification and labelling that defines the useful life of ultrasound transducers in the field.

    Product
    Philips L12-5 Ultrasound Transducer
    Category
    Medical Device
    Distribution
    Distributed nationwide