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. 2,510 recalls have been distributed to Nevada in the last 12 months.

50,223 total recalls
2,510 in last 12 months

Showing 2516125180 of 28,334 recalls

Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ATTAIN HYBRID¿ Guide Wire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: Zinger¿ Stainless Steel Workhorse Guidewire Recalled by Medtronic Vascular...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Medtronic Vascular

Recalled Item: ZINGER¿ Steerable Guidewire Recalled by Medtronic Vascular Due to Potential...

The Issue: Potential for PTFE (polytetrafluroethylene) coating to delaminate and detach...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 21, 2013· Intuitive Surgical, Inc.

Recalled Item: da Vinci Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive has identified that the metalized coating on the IS3000 HD lamp...

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

Class III — Low RiskOngoing
Medical DeviceOctober 18, 2013· Advanced Sterilization Products

Recalled Item: Sterrad 100NX Recalled by Advanced Sterilization Products Due to Advanced...

The Issue: Advanced Sterilization Products (ASP) is recalling the Sterrad 100NX...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2013· Steris Corporation

Recalled Item: AMSCO¿ Evolution¿ steam sterilizer Transfer Carriage. Product Usage: Mobile...

The Issue: The firm discovered that unlatching can occur when overloaded transfer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2013· Intra Pump Infusion Systems

Recalled Item: CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle" Recalled by Intra Pump...

The Issue: Product has the potential to have a clear debris on the tip of the needle.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Baxter Healthcare Corp

Recalled Item: 15 L Cycler Drainage Bag Product Usage: For use with Recalled by Baxter...

The Issue: The large tube clamp used to close the drain tube on the 15 L Cycler...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Spacelabs Healthcare, Llc

Recalled Item: Spacelabs Healthcare qube Compact Patient Monitor Recalled by Spacelabs...

The Issue: Spacelabs Healthcare qube Compact Patient Monitor, Model 91390, may fail to...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Del Mar Reynolds Medical, Ltd.

Recalled Item: CAS I/II Absorbers that are parts of the BleaseSirius Anesthesia Workstation...

The Issue: Spacelabs Healthcare Ltd. of United Kingdom recalls , and Service Kits, Part...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 17, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal" Reverse Shoulder System Recalled by Zimmer, Inc. Due to As...

The Issue: As a result of complaints for disassociation of the TM Reverse Glenosphere...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 2 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Philips Medical Systems North America Inc.

Recalled Item: EPIQ 7 Ultrasound System Recalled by Philips Medical Systems North America...

The Issue: A problem has been detected with Philips Model EPIQ 7 Ultrasound System,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· GlaxoSmithKline, LLC.

Recalled Item: Biotene Moisturizing Mouth Spray Recalled by GlaxoSmithKline, LLC. Due to...

The Issue: Label indicates, "Sweetened with xylitol and Sorbitol", however product does...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Na+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Baxter Healthcare Corp.

Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...

The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch &...

The Issue: Lens was manufactured with incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Cutera, Inc.

Recalled Item: Cutera brand truSculpt infrared System (optional) Recalled by Cutera, Inc....

The Issue: Cutera received two adverse events associated with the edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Teleflex Medical

Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...

The Issue: One material batch used for production of the affected parts of the Synthes...

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

Class II — Potential Health HazardOngoing