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.

50,223 total recalls
1,792 in last 12 months

Showing 3406134080 of 50,223 recalls

DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: 3rd DEGREE capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sibutramine.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 29, 2016· Making It a Lifestyle

Recalled Item: BLACK LABEL X capsules Recalled by Making It a Lifestyle Due to Undeclared...

The Issue: Marketed without an approved NDA/ANDA - presence of undeclared sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...

The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...

The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...

The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
DrugApril 28, 2016· Lymol Medical

Recalled Item: Sclerosol Intrapleural Aerosol (sterile talc powder) Recalled by Lymol...

The Issue: Defective Delivery System: Defective stem valve causes leakage of the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2016· Pfizer Inc.

Recalled Item: Zoloft (sertraline HCl) tablets Recalled by Pfizer Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: thick tablets exceeding specifications...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 28, 2016· Excelsior Medical Corp

Recalled Item: Excelsior Disposable Syringe Heparin Lock Flush Recalled by Excelsior...

The Issue: Certain lots of Heparin Lock Flush, USP Syringes (5 ml Fill in 10 ml...

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

Class II — Potential Health HazardOngoing
DrugApril 27, 2016· Novo Nordisk Inc

Recalled Item: Norditropin FlexPro Somatropin (rDNA origin) injection Recalled by Novo...

The Issue: Defective Delivery System; may have a low frequency assembly fault which may...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 27, 2016· Teva North America

Recalled Item: Linezolid Injection Recalled by Teva North America Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Due to potential for leaking bags.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 27, 2016· World's Choice Products

Recalled Item: Choice Products Supreme Elixir 32oz. Recalled by World's Choice Products Due...

The Issue: Undeclared whey protein which contains milk and soy lecithin.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 27, 2016· World's Choice Products

Recalled Item: New Life Nature's Blend 100% Multivitamin Juice 32oz. Recalled by World's...

The Issue: Undeclared whey protein which contains milk and soy lecithin.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 27, 2016· World's Choice Products

Recalled Item: Choice Products. Xtreme Fiber Detox Net. Wt. 1lb Net Wt. 8oz. Recalled by...

The Issue: Undeclared whey protein which contains milk and soy lecithin.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 27, 2016· Mighty Leaf Tea

Recalled Item: Mighty Leaf Tea Company Organic Ginger Peach Iced Tea Recalled by Mighty...

The Issue: Firm was notified by their supplier of Organic Ginger Peach tea that it has...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 27, 2016· Orthofix, Inc

Recalled Item: Firebird NXG Spinal Fixation System Set Screw Driver used to Recalled by...

The Issue: There is a possibility that the subject set screw driver could disengage...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· Greiner Bio-One North America, Inc.

Recalled Item: 4 ml FX Sodium Fluoride/Potassium Oxalate tube Recalled by Greiner Bio-One...

The Issue: The 4 ml FX Sodium Fluoride/Potassium Oxalate tube may have no or low...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 26, 2016· STERILMED, INC.

Recalled Item: Reprocessed Microline Scissor Tips intended to be used with a Recalled by...

The Issue: Sterlilmed is recalling all unexpired Scissor Tips because of a potential...

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

Class II — Potential Health HazardOngoing