Product Recalls in Nevada
Product recalls affecting Nevada — including food, drugs, consumer products, medical devices, and vehicles distributed to Nevada. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,684 recalls have been distributed to Nevada in the last 12 months.
Showing 8121–8140 of 50,223 recalls
Recalled Item: Cardioplegia Solution del Nido Formula Recalled by Central Admixture...
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CARDIOPLEGIA SOLUTION Recalled by Central Admixture Pharmacy Services, Inc....
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neonatal TPN Starter Bag Recalled by Central Admixture Pharmacy Services,...
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neonatal TPN Starter Bag Recalled by Central Admixture Pharmacy Services,...
The Issue: Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SOZO Bilateral Arm L-Dex Software Recalled by Impedimed Limited Due to...
The Issue: Bilateral L-Dex assessment software does not have the same level of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: exoplan version 3.1 Rijeka Software -A medical software Recalled by Exocad...
The Issue: A software library filtering error has been discovered which occurs when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient Information Center iX with Software Version Number 4.x in Recalled...
The Issue: Patient Information Center (PIC iX) Release 4.x Surveillance Crash Caused by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nexlizet (bempedoic acid and ezetimibe) Recalled by Esperion Due to Failed...
The Issue: Failed dissolution specifications: below specification results at stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Power Snacks Honey Roasted Sunflower Kernels Recalled by Mount Franklin...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1. 7 Select Cashews Halves & Pieces Honey Roasted Recalled by Mount Franklin...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Circle K Honey Roasted Peanuts Recalled by Mount Franklin Foods LLC DBA Azar...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 1. Circle K Get Up Trail Mix Recalled by Mount Franklin Foods LLC DBA Azar...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Circle K Sweet & Spicy Mix Recalled by Mount Franklin Foods LLC DBA Azar Nut...
The Issue: Potential to contain undeclared soy and/or wheat allergen due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Procedure pack: Presource PBDS Cat. PLMHCSBHF Recalled by Cardinal Health...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure pack: Presource PBDS Recalled by Cardinal Health 200, LLC Due to...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump Recalled by Smiths Medical ASD Inc. Due to A force...
The Issue: A force sensor in the occlusion detector may drift out of calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource Pain Tray Recalled by Cardinal Health 200,...
The Issue: Packs contain recalled components (equipment drapes, table cover, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Procedure packs: (1) Presource PBDS Cat. PN33BPCR2 Recalled by Cardinal...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.