Recalls affecting Nevada
Notices that name Nevada in their distribution area, plus every nationwide recall — nationwide recalls reach Nevada too.
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Class II · 18 days ago
Amneal Pharmaceuticals, LLC Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton recall: Defective Container; packets were found to be either empty or partially full
Defective Container; packets were found to be either empty or partially full.
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Class I · 18 days ago
Todd's Seeds LLC Todd's Seeds Alfalfa Sprouting Seeds, packaged in heat-sealed recall: Products contain alfalfa seed recalled by the supplier
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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Class I · 18 days ago
Todd's Seeds LLC Todd's Seeds Sprouting Seed Mix - Broccoli, Radish, Alfalfa recall: Products contain alfalfa seed recalled by the supplier
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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Class I · 18 days ago
Todd's Seeds LLC Todd's Seeds Alfalfa & Mung Bundle recall: Products contain alfalfa seed recalled by the supplier
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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Class I · 18 days ago
Todd's Seeds LLC Todd's Seeds Variety Pack of Sprouting Seeds - Broccoli recall: Products contain alfalfa seed recalled by the supplier
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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Class I · 18 days ago
Todd's Seeds LLC Todd's Seeds Broccoli & Friends Sprouting Seed Mix - Broccoli recall: Products contain alfalfa seed recalled by the supplier
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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Class I · 18 days ago
Todd's Seeds LLC Todd's Seeds Salad Sprouting Mixture - Broccoli, Mustard recall: Products contain alfalfa seed recalled by the supplier
Products contain alfalfa seed recalled by the supplier and may be contaminated with E. coli and/or Salmonella (downstream recall)
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NHTSA safety recall · 19 days ago
Ford recall: The analog cluster’s tachometer and speedometer may become stuck or move
The analog cluster’s tachometer and speedometer may become stuck or move erratically, providing inaccurate readings to the driver. As such, these…
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NHTSA safety recall · 23 days ago
Mercedes-Benz recall: The front brake hoses may rupture and leak brake fluid
The front brake hoses may rupture and leak brake fluid.
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NHTSA safety recall · 24 days ago
Honda VT1300CX and VT750 recall: The fuel pump may malfunction due to a manufacturing defect
The fuel pump may malfunction due to a manufacturing defect.
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Highest risk · 24 days ago
Kobayashi Rechargeable Hand Warmers recall: Risk of Serious Injury from Fire and Burn Hazards
Risk of Serious Injury from Fire and Burn Hazards
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Elevated risk · 24 days ago
Gazelle USA Urban Arrow Cargo Electric Bikes recall: Fall Hazard
Fall Hazard
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Highest risk · 24 days ago
Dollar Tree Stores Electric Balloon Pumps recall: Burn Hazard
Burn Hazard
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Highest risk · 24 days ago
ABC Trading Squishy Toys recall: Risk of Serious Injury or Death from Water Bead Ingestion
Risk of Serious Injury or Death from Water Bead Ingestion; Violate Mandatory Standard for Toys
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NHTSA safety recall · 25 days ago
Volkswagen ID.4 recall: 4 vehicles. The high voltage battery may fail and lead to a vehicle fire
4 vehicles. The high voltage battery may fail and lead to a vehicle fire.
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Class II · 25 days ago
Medline Convenience Kits: 1) Major Pack recall: The kits contain neurological sponges with the potential for unexpected
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may…
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Class II · 25 days ago
Medline Convenience Kits: 1) Peds Sinus Pack recall: The kits contain neurological sponges with the potential for unexpected
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may…
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Class II · 25 days ago
Philips North America Llc SmartPath to dStream for 1.5T, SmartPath to dStream for 3.0T recall: A software issue will terminate an examination during the image
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that…
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Class II · 25 days ago
Philips North America Llc Achieva 1.5T, Achieva 1.5T Conversion and Achieva 1.5T recall: A software issue will terminate an examination during the image
A software issue will terminate an examination during the image reconstruction process if the scan parameters are manually adjusted such that…
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Class II · 25 days ago
Medline Convenience Kits: 1) MFC Craniotomy Pack recall: The kits contain neurological sponges with the potential for unexpected
The kits contain neurological sponges with the potential for unexpected variability of endotoxin levels. Potentially elevated endotoxin levels may…
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Class II · 25 days ago
Baxter Healthcare Corporation PRO+ 36" MRS Surface recall: There is an error in the product description on the Unique Device
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the…
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Class II · 25 days ago
Baxter Healthcare Corporation PRO+ MRS Surface FOR Versacare recall: There is an error in the product description on the Unique Device
There is an error in the product description on the Unique Device Identification (UDI) label. These discrepancies in labeling do not align with the…
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Class II · 25 days ago
Baxter Healthcare Corporation Brand Name: Volara System Product Name: Volara, HC recall: Contamination within the release test equipment flow path could have affected
Contamination within the release test equipment flow path could have affected the accuracy of the nebulizer flow rate. Affected devices returned to…
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Class II · 25 days ago
Becton, Dickinson and Company ForeSight Elite Tissue Oximetry Cable REF Hemfsm10 recall: Due to incorrect switching of Channel 1 and 2 on the module and flag labels
Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.