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. 1,792 recalls have been distributed to Nevada in the last 12 months.
Showing 34921–34940 of 50,223 recalls
Recalled Item: Dextroamphetamine Saccharate Recalled by Actavis Elizabeth LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...
The Issue: Presence of Particulate Matter: Glass particles found in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Thyrogen (thyrotropin alfa for injection) Recalled by Genzyme Corporation...
The Issue: Presence of Particulate Matter: Glass particles found in the product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 4.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.5 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cannulated Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.0 mm and 7.3 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5 mm Cancellous Screw Recalled by Synthes (USA) Products LLC Due to...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 mm and 4.0 mm Cannulated Screw Recalled by Synthes (USA) Products LLC...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4.0 mm Cortex Screw Recalled by Synthes (USA) Products LLC Due to Labeling...
The Issue: Labeling does not match the cleared indications for use in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The...
The Issue: Siemens Healthcare Diagnostics has determined that Dimension Vista Blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: The two sets of wires (4 total wires) exiting from the EMI filters were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CIOS ALPHA (Image-intensified fluoroscope x-ray system) Product Usage: The...
The Issue: Siemens found a defective part in their production line which could increase...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Interlocking Bolt Recalled by Synthes (USA) Products LLC Due to...
The Issue: DePuy Synthes is initiating a voluntary medical device recall of certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fruit & Nut Medley Recalled by King Henry's, Inc. Due to Undeclared Fd
The Issue: King Henry is recalling Fruit and Nut Medley because it may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens branded SOMATOM Emotion and SOMATOM Sensation families of CT...
The Issue: Siemens is initiating this recall due to a potential malfunction and hence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.