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. 1,025 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,025 in last 12 months

Showing 21461–21480 of 50,223 recalls

Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 1000 Progesterone Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: There is a potential for low discordant progesterone results on a subset of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2019· Phadia Ab

Recalled Item: Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is Recalled by...

The Issue: code 7-102 Liquid Sensor Error

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

Class II — Potential Health HazardOngoing
DrugJuly 9, 2019· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Drospirenone and Ethinyl Estradiol Tablets Recalled by Jubilant Cadista...

The Issue: Failed dissolution specifications : failed results at the 3-month stability...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Wholeberry Blast Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Chocolate Coconut Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Superfood Slam Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR The Simply Real Bar: Chocolate Coconut Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Peanut Butter Chocolate Chip Recalled by Probar LLC Due to...

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 9, 2019· Probar LLC

Recalled Item: PROBAR MEAL Original Trail Mix Recalled by Probar LLC Due to Undeclared Milk

The Issue: Chocolate chip containing meal bars potentially contain undeclared milk and soy

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5600 Integrated System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 350 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250 Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho Clinical Diagnostics Due to Potential...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 32 Recalled by Ortho Clinical...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Ortho Clinical Diagnostics

Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho Clinical Diagnostics Due to...

The Issue: Potential Unsuccessful Calibration Due to Software Anomaly in VITROS System

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2019· Smiths Medical ASD Inc.

Recalled Item: GRIPPER Needles sold individually. Labeled as the following item...

The Issue: Potential for certain GRIPPER Needles to contain an occluded or blocked needle.

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

Class II — Potential Health HazardOngoing