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. 2,722 recalls have been distributed to Nevada in the last 12 months.
Showing 2261–2280 of 50,223 recalls
Recalled Item: Philips VL13-5 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L8-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L9-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips S7-3t Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe...
The Issue: Due to an error in assembly of the thermistor within some units, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Long Nail Recalled by Stryker GmbH Due to Investigation confirmed that the...
The Issue: Investigation confirmed that the GAMMA4 Right Long Nail was manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion R1.x and R2.x systems Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...
The Issue: A software issue was identified in the internal communication process...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Fresenius Medical Care Holdings,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluoxetine Tablets Recalled by Torrent Pharma Inc. Due to CGMP Deviations:...
The Issue: CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: O-arm O2 Imaging System. Mobile X-Ray System. Recalled by Medtronic...
The Issue: A mechanical component that supports the O2 gantry to the support structure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STICK Recalled by Microbiologics Inc Due to Affected products were...
The Issue: Affected products were packaged with the incorrect KWIK STIK assembly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Barco MNA with the HexaVue IP Integration System Recalled by Steris...
The Issue: This is a sub-recall of event RES 96885. The supplier identified that during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoclopramide Tablets Recalled by Teva Pharmaceuticals USA, Inc Due to...
The Issue: Presence of foreign tablets/capsules.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories, LLC Due to...
The Issue: Failed Impurities/Degradation Specifications An out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cephalexin for Oral Suspension Recalled by Ascend Laboratories, LLC Due to...
The Issue: Failed Impurities/Degradation Specifications An out-of-specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Spectrum Advanced Gel Hand Sanitizer Recalled by Consumer Product Partners,...
The Issue: Subpotent product: Product has cloudy appearance and tested below assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SIGNA Architect Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect AIR Recalled by GE Medical Systems, LLC Due to GE HealthCare...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA PET/MR Recalled by GE Medical Systems, LLC Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that gradient coils for certain MR systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.