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. 2,684 recalls have been distributed to Nevada in the last 12 months.
Showing 8281–8300 of 50,223 recalls
Recalled Item: Membrane Changer Single-Use Recalled by SenTec AG Due to During rework of...
The Issue: During rework of components during the manufacturing process, an additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVU Functional GI Software Recalled by Diversatek Healthcare Due to GI...
The Issue: GI Software labelled as revision 3.3.0 is incorrectly labeled and is in fact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The O-arm O2 Imaging System is a mobile x-ray system Recalled by Medtronic...
The Issue: Ground cable installed incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Lead Clipper- An auxiliary tool indicated for use in Recalled by Cook...
The Issue: Sterility of device may be compromised due to breach of the chevron seal of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cromolyn Sodium Oral Solution (Concentrate) 100 mg/5 mL 96 Plastic Recalled...
The Issue: CGMP deviation: product released prior to supplier approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...
The Issue: cGMP deviations: Batch was released prior to approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rufinamide Tablets Recalled by Aurobindo Pharma USA Inc. Due to cGMP...
The Issue: cGMP deviations: Batch was released prior to approval.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is Recalled by Ambu Inc. Due...
The Issue: Multiple impacts, for example from being dropped, can cause to the Ambu...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Keystone Bosworth Copaliner Cavity Varnish .5oz (14 ml)- Intended to...
The Issue: A bottle of Copaliner Solvent was inadvertently packaged into a box labeled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zenition 70. The device is to be used in health Recalled by Philips Medical...
The Issue: Philips has become aware of the potential for unintended radiation exposure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cosmedent FlexiCup Composite Finishing & Polishing System Recalled by...
The Issue: Reports were received the elastomer cup material is crumbling.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: For intraventricular indications mainly used for operations within the brain...
The Issue: Trocar manufactured with the shaft too long and does not meet manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visera Hysterovideoscope Olympus HYF Type V Recalled by Olympus Corporation...
The Issue: IFU labeling is being updated to revise EtO gas mixture and elimination of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHOROPTOR VRX DIGITAL SYSTEM-Digital intended for the subjective Recalled by...
The Issue: Phoroptor VRx Head may detach from the bracket that connects the Phoroptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tim Heung Yuen Black Melon Seed 6 oz. Recalled by Richin Trading Inc Due to...
The Issue: Undeclared allergens; soy and wheat
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NOxBOXi Nitric Oxide Delivery System Recalled by NOXBOX LTD Due to...
The Issue: Replacement of the internal Sample Pump due to high failure rates.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freedom Boom models series: F110 Recalled by IHB OPERATIONS B.V. Due to...
The Issue: Weakened connection point on the adjustable suspension arm, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper series Recalled by Philips Medical Systems Nederland B.V. Due to...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion Recalled by Philips Medical Systems Nederland B.V. Due to A foot...
The Issue: A foot switch pedal may get stuck in the active position when the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.