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 9241–9260 of 50,223 recalls
Recalled Item: ICD CROME VR MRI DF4 Recalled by Medtronic Inc., Cardiac Rhythm and Heart...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD COBALT XT VR MRI DF4 Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRT-D DTBC2Q1 BRAVA QUAD IS4/DF1 INTL Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-VR DVAB1D1 VISIA AF US IS1/DF1 Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD CROME HF QUAD MRI IS4 DF4 Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-VR DVAB1D4 VISIA AF US DF4 Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ICD COBALT VR MRI IS1 DF1 Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRTD DTPA2D1G COBALT XT HF QUAD OUS Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRT-D DTBB2Q1 VIVA QUAD S IS4/DF1 INTL Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CRT-D DTBA2D4 VIVA XT IS1/DF4 INTL Recalled by Medtronic Inc., Cardiac...
The Issue: There is a rare potential for reduced- or no-energy output during high...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Walnut Wearable Smart Thermometer Recalled by BearCare, Inc. Due to There...
The Issue: There have been reports of skin burns to children wearing the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: buPROPrion Hydrochloride Extended-Release Tablets Recalled by SUN...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Heparin Sodium Recalled by B. Braun Medical Inc Due to Subpotent: Low...
The Issue: Subpotent: Low anti-factor IIa Potency.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Black Fungus Golden Koi 2.5 oz packages 100 bags per Recalled by AH USA...
The Issue: Product may contain salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vRad PACS with Mammography Recalled by Virtual Radiologic Corp. Due to The...
The Issue: The error resulted in intermittent failure of current (primary) radiology...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Methylprednisolone Acetate Injectable Suspension Recalled by Amneal...
The Issue: Labeling: Not Elsewhere Classified; A typographical error was observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only....
The Issue: Potential to cause biased results in the upper end of the reportable range...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tearaway Introducer Kit Recalled by Galt Medical Corporation Due to Sheath...
The Issue: Sheath introducer assemblies could potentially, due to improper storage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Tempus LS-Manual Defibrillator Recalled by Remote Diagnostic...
The Issue: Defibrillator/pacemaker module (DPM) may encounter a problem causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.