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. 986 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
986 in last 12 months

Showing 30901–30920 of 50,223 recalls

Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint - 3R Recalled by Siemens Medical Solutions USA Inc....

The Issue: The mobile-specific instructions was not shipped to a limited population of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza Recalled by Siemens Medical Solutions USA, Inc Due to Software...

The Issue: Software updates

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.

Recalled Item: AMS-636 Recalled by Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc....

The Issue: Incorrect priming volume printed on the device package.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 20, 2017· CareFusion 303, Inc.

Recalled Item: MaxGuard Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the MaxGuard Extension Set due to reports of leaks...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Custom parts Product Usage: Custom Recalled by...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Sports Med Repicci II Tibial Components...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Extremities Recalled by Zimmer Biomet, Inc....

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Knees Revision Tibial Tray Systems Oxford...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 17, 2017· Zimmer Biomet, Inc.

Recalled Item: various polyethylene implants Hips Active Articulation ArComXL Bearings...

The Issue: Endotoxin levels higher than process maximum limits were discovered in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodFebruary 17, 2017· Diamond Crystal Brands Inc

Recalled Item: Natural Cocoa Powder 10-12% cocoa butter Recalled by Diamond Crystal Brands...

The Issue: During sanitation, the firm discovered metal pieces missing from a sifter...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 17, 2017· Diamond Crystal Brands Inc

Recalled Item: Baking Powder Net Wt. 5 lbs. (2.27 kg) packaged 6 bags per case Recalled by...

The Issue: During sanitation, the firm discovered metal pieces missing from a sifter...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 17, 2017· Diamond Crystal Brands Inc

Recalled Item: Natural Cocoa Powder 22-24% cocoa butter Recalled by Diamond Crystal Brands...

The Issue: During sanitation, the firm discovered metal pieces missing from a sifter...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: VANCOMYCIN HCl 1.5g in 300 mL 0.9% Sodium Chloride Injection USP Recalled by...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2017· Teva Pharmaceuticals USA

Recalled Item: Risedronate Sodium Delayed-release Tablets Recalled by Teva Pharmaceuticals...

The Issue: Failed Dissolution Specifications: low out of specification dissolution...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP Recalled by...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium CHLORide added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 17, 2017· Pharmedium Services, LLC

Recalled Item: Potassium PHOSphate added to 0.9% Sodium Chloride Recalled by Pharmedium...

The Issue: Labeling: Not Elsewhere Classified: Incorrect volume printed on the product...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund