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. 2,608 recalls have been distributed to Nevada in the last 12 months.
Showing 16801–16820 of 28,334 recalls
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen CVC Kit Recalled by Arrow International Inc...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Sheath Introducer Kit with ARROWg+ard Blue Sheath Recalled by...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with...
The Issue: Products do not contain the Central Venous Catheter Placement Procedures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triage Drugs of Abuse Plus TCA 25 Test Kit Recalled by Alere San Diego, Inc....
The Issue: The recalled lots have demonstrated unexpected false positive THC results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 4000 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 3010 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion Syringe Pump 3500 Series The Medfusion¿ Syringe Infusion Pumps...
The Issue: Certain Medfusion Syringe Pump Models, Series 3100, 3500, and 4000, may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Piranha Screw 4.0 x 12mm Recalled by Amendia, Inc dba Spinal Elements Due to...
The Issue: Potential incorrect marking and color identification of Piranha screw. Some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100...
The Issue: iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage PureFlow B Solution - Premixed Dialysate for Hemodialysis with...
The Issue: Using different fluid formulations of NxStage PureFlow B Solution at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOOG Curlin Infusion Administration Set Recalled by Zevex Incorporated (dba...
The Issue: Particulate found on the Curlin spike.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClariVein IC infusion catheter Recalled by Vascular Insights, LLC Due to...
The Issue: Certain catheters could have a compromised catheter shaft due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista System LOCI 8 CALIBRATOR The LOCI 8 Calibrator Recalled by...
The Issue: An increase in the number of failed calibration events or negative bias with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.