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. 2,651 recalls have been distributed to Nevada in the last 12 months.
Showing 13601–13620 of 28,334 recalls
Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER Recalled by Bard Peripheral...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet Recalled by...
The Issue: The action is being initiated due to complaints received concerning the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVACLEAR 400 Dialyzer Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVACLEAR 300 Dialyzer Recalled by Baxter Healthcare Corporation Due to...
The Issue: There is a potential presence of ruptured dialyzer fibers which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLEO Patient Monitor /Tranquility VS Patient Monitor Recalled by Infinium...
The Issue: The CLEO & Tranquility VS Patient Monitors 510(k) indications for use in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitinol Thermocouple Electrode Recalled by Boston Scientific Neuromodulation...
The Issue: The firm initiated a voluntary correction of certain Cosman TCN Electrodes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold Recalled by Galemed...
The Issue: Reports of pressure relief manifold venting gas below the standard pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babi.Plus Bubble PAP Valve with 12.5 cm H2O Pressure Relief Manifold...
The Issue: Reports of pressure relief manifold venting gas below the standard pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Babi.Plus 12.5 cm H2O Pressure Relief Manifold with Gas Supply Recalled by...
The Issue: Reports of pressure relief manifold venting gas below the standard pressure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.