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. 1,005 recalls have been distributed to Nevada in the last 12 months.
Showing 28221–28240 of 50,223 recalls
Recalled Item: Spectranetics Bridge Occlusion Balloon catheter Recalled by Spectranetics...
The Issue: Possible inability to pass the guidewire through the Bridge device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Hip Application (THA) Product Usage: The Robotic Arm Interactive...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Unity software Recalled by Merge Healthcare, Inc. Due to The software...
The Issue: The software is not identifying the patient as having atypical hyperplasia,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pravastatin Sodium Tablets Recalled by International Laboratories, Inc. Due...
The Issue: Labeling: Label mix-up, the product labeled as Pravastatin sodium tablets 40...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quillivant XR methylphenidate HCl Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneStep CPR Complete Recalled by ZOLL Medical Corporation Due to A portion...
The Issue: A portion of one lot of ZOLL OneStep Complete Electrodes for adults will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultradent Products Recalled by Ultradent Products, Inc. Due to The barcode...
The Issue: The barcode label was placed underneath the sterile barrier and the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Recalled by...
The Issue: The 7mm diameter uniaxial pedicle screws have been color anodized with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitamin A&D Ointment (petroleum 93.5%) Recalled by MEDLINE INDUSTRIES INC...
The Issue: Labeling Mixup; the individual A&D ointment foil packets are incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lorazepam Oral Concentrate Recalled by Amneal Pharmaceuticals of New York,...
The Issue: Defective Delivery System: the dropper measurement markings may be reversed,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine HCL Capsules Recalled by KVK-Tech, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: out-of-specification results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby Aller-chlor (Chlorpheniramine Maleate Syrup Recalled by The Harvard...
The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rugby Senexon Liquid Natural Vegetable Stimulant Recalled by The Harvard...
The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major Senna Syrup Natural Vegetable Laxative Recalled by The Harvard Drug...
The Issue: Microbial contamination of Non-sterile Products; presence of yeast and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.