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 8301–8320 of 50,223 recalls
Recalled Item: MultiDiagnost-Eleva Recalled by Philips Medical Systems Nederland B.V. Due...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fosfomycin Tromethamine Granules for Oral Solution Recalled by Ascend...
The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dofetilide Capsules 500 mcg (0.5mg) Recalled by SUN PHARMACEUTICAL...
The Issue: Out of Specification result observed in content uniformity testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Proclaim" XR 7 Implantable Pulse Generator (previously known Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 5 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim XR 5 Implantable Pulse Genterator (previously known Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 5 Implantable Pulse Generator Product Description: The Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinity 7 Implantable Pulse Generator Product Description: The Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim DRG Implantable Pulse Generator Product Description: The Recalled...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proclaim Plus 7 Implantable Pulse Generator Product Description: Recalled by...
The Issue: Firm has received complaints from patients who are unable to exit MRI...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX 0.5u HYDROPHOBIC DISC FILTER Recalled by Smiths Medical ASD Inc. Due...
The Issue: Smiths Medical identified a labeling error in which the barcode (UDI) was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: succinylcholine Recalled by Central Admixture Pharmacy Services Inc Due to...
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: morphine in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
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: HYDROmorphone in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
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: morphine in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
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: fentaNYL in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...
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: midazolam in dextrose 5% 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: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...
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: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...
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: HYDROmorphone added to 0.9% sodium chloride 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.