Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,466 recalls have been distributed to Nebraska in the last 12 months.
Showing 21941–21960 of 49,150 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: Strawberry Banana Smoothie Recalled by Stonyfield Farm Due to Mislabeling
The Issue: Strawberry Banana Smoothie Drink outside plastic wrap is mislabeled with...
Recommended Action: Do not consume. Return to store for a refund or discard.
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: BD Vacutainer Fluoride Tubes for Blood Alcohol determinations Part Number:...
The Issue: Lot has been confirmed to have no additive within the tube. Sample processed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anti-fog solution packaged in a Tyvek peel pouch and it Recalled by Medline...
The Issue: The Anti-Fog Solution may not defog properly due to a degradation in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.