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.
Showing 49981–50000 of 50,223 recalls
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console Recalled by The Anspach Effort, Inc. Due to The...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******eMax 2 Plus Console***SN G 10307653002*** Product Usage: The Recalled...
The Issue: The RPM of the Motor Handpiece may be less than 80,000 RPM.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Nasal Solution Recalled by Apotex Corp. Due to CGMP...
The Issue: CGMP Deviations: tubing used for filling may interact with the nasal...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Z-800 Volumetric Infusion System. For intravenous infusion of parenteral...
The Issue: Update Instruction For Use for Preventative Maintenance (PM) Schedule and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian High Energy Clinacs Recalled by Varian Medical Systems, Inc. Oncology...
The Issue: Under certain conditions, photon beams in High Energy Clinacs may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty Pouch Clean & Dry External Male Catheter Specialty Recalled...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Safe n' Dry 21006 (Component: SKIN-PREP Protective wipes). The...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component (Smith...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioDerm Liberty 3.0 External Male Catheter Specialty Type with integral...
The Issue: On 06/08/2011, BioDerm, Inc. issued a voluntary recall of a component skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vegi-Fiber Plus Recalled by Wynlife Healthcare, Inc. Due to Wynlife...
The Issue: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: All-In-One Probiotics Recalled by Wynlife Healthcare, Inc. Due to Wynlife...
The Issue: Wynlife healthcare is recalling their All-In-One Probiotics and Vegi-Fiber...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: PIRACETAM POWDER COGNITION ENHANCING AGENT Dietary Supplement CTD 500 grams...
The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PIRACETAM COGNITION ENHANCING AGENT Dietary Supplement PHARMACEUTICAL GRADE...
The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ANIRACETAM FAST ACTING NOOTROPIC Dietary Supplement PHARMACEUTICAL GRADE...
The Issue: Marketed Without an Approved NDA/ANDA: The product is an unapproved new drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~120V ~ 60 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neptune¿ 2 Rover - ULTRA ~230V ~ 50 Hz 12A Recalled by Stryker Instruments...
The Issue: Beginning May 24, 2011 Stryker Neptune 2 (N2) Waste Management Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Universal Light Source...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******Qty 1*** EC REP*** ConMed Linvatec Xenon Light Source Recalled by...
The Issue: Linvatec Corporation dba ConMed Linvatec, Largo, FL initiated a recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare reported a...
The Issue: GE Healthcare reported a potential safety issue due to temporary loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.