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. 1,712 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
1,712 in last 12 months

Showing 4800148020 of 50,223 recalls

Medical DeviceOctober 18, 2012· OrthoPediatrics Corp

Recalled Item: 4.5mm PLEO Osteotomy Guide. OrthoPediatrics Corp. markets a pediatric...

The Issue: Complaint received from sales representative that the drill guide tubes...

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

Class II — Potential Health HazardOngoing
FoodOctober 17, 2012· Energy Club Inc

Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...

The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 17, 2012· Energy Club Inc

Recalled Item: Peanuts in Shell Recalled by Energy Club Inc Due to Potential Salmonella...

The Issue: Trifecta Foods, LLC in Pacoima, CA is voluntarily recalling products...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 17, 2012· Biomerieux Inc

Recalled Item: 0.9% Sodium Chloride Injections Recalled by Biomerieux Inc Due to The firm...

The Issue: The firm inventoried and distributed 0.9% Sodium Chloride Saline bags as...

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

Class II — Potential Health HazardOngoing
FoodOctober 16, 2012· Torn & Glasser Inc.

Recalled Item: Organic Peanut Butter Recalled by Torn & Glasser Inc. Due to Potential...

The Issue: Torn and Glasser, Inc of Los Angeles, CA 90021 is voluntarily recalling...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 16, 2012· Torn & Glasser Inc.

Recalled Item: Salted in-shell Peanuts under the following. Salted in Shell PeanutsGless...

The Issue: Torn and Glasser, Inc of Los Angeles, CA 90021 is voluntarily recalling...

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 16, 2012· Mondelez Global Llc

Recalled Item: Green & Black's Organic Peanut & Sea Salt Milk Chocolate Recalled by...

The Issue: Mondelez Global LLC (Mondelez Global) is voluntarily recalling the U.S....

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

Class I — Serious Health HazardOngoing
Refund
FoodOctober 16, 2012· PureFit Inc

Recalled Item: PureFit Peanut Butter Bars Recalled by PureFit Inc Due to Potential...

The Issue: PureFit is recalling PureFit Peanut Butter Crunch Bars because of possible...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0 A fetal...

The Issue: Thirty fetal scalp electrodes were found to have an incomplete package seal...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2012· Biomerieux Inc

Recalled Item: bioMerieux Kit Recalled by Biomerieux Inc Due to Mislabeling

The Issue: The product may mislabel patient information on culture specimen bottles due...

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

Class II — Potential Health HazardOngoing