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. 2,608 recalls have been distributed to Nevada in the last 12 months.
Showing 16141–16160 of 28,334 recalls
Recalled Item: Arrow-Johans" ECG Adapter for Right Atrial Electrocadiography (RAECG)...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue(R) Central Venous Catheterization Kit Recalled by Arrow...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0.2 Micron Flat Epidural Filter Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuous Nerve Block Needle Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Injectable Quad-Lumen Central Venous Catheterization Kit with Blue...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9 Fr. Radiopaque Polyurethane Sheath/Dilator with Integral Hemostasis...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWgard Blue PLUS¿ Multi-Lumen CVC Kit with Blue FlexTip¿ Catheter...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catheter Hemostasis Valve For use with .038" (.096 cm) dia. Recalled by...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow PICC with Chlorag+ard Technology Recalled by Arrow International Inc...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW PICC Set Recalled by Arrow International Inc Due to Product sterility...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clear Fenestrated Drape with Adhesive Recalled by Arrow International Inc...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue¿ PSI Kit with Integral Hemostasis Valve/ Side Port Recalled...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echogenic Introducer Needle Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: Product sterility may be compromised due to unsealed packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD Systems 600 Series Washer/Pasteurizer Recalled by Cenorin, LLC Due to...
The Issue: There is a supplier quality issue with the terminal blocks which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 4.8MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EEA" Hemorrhoid and Prolapse Stapler Set with DST Series" Technology 3.5MM...
The Issue: There is a potential for improper welding of the yellow staple guide to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TN Plate Recalled by Orthofix, Inc Due to Firm is conducting a voluntary...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM Recalled by Orthofix,...
The Issue: Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.