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. 1,070 recalls have been distributed to Nevada in the last 12 months.
Showing 13901–13920 of 50,223 recalls
Recalled Item: The DIXI Medical Microdeep Depth Electrode ( Microdeep Depth Electrode or...
The Issue: Potential deformation of the internal packaging (blister pack) could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...
The Issue: There is a high risk of the blue hub detaching from the corkscrew needle,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R82 by ETAC Push Brace for High-Low Recalled by R82 A/S Due to The chrome...
The Issue: The chrome surface of the push brace can crack during use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brinzolamide Ophthalmic Suspension Recalled by Teva Pharmaceuticals USA Due...
The Issue: Defective Container: The notch in the cap that fits into the nozzle of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diclofenac Sodium Topical Solution 1.5% Recalled by Direct Rx Due to...
The Issue: Defective Container: Leaking containers.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 6 Part Number: 11000610 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 8 Part Number: 110008600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 12 Product Code: 110012100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 16 Product Code: 110016100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE REV STEM SZ 10 Product Code: 110010600 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novalung Sensor Box (F30000163) a component of Novalung Console (F30000162)-...
The Issue: Error messages 206 (yellow) and 208 (red) technical failure, flow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 8 Part Number: 110008100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL UNITE STD STEM SZ 14 Product Code: 110014100 Recalled by DePuy...
The Issue: Stems may have an undersized spigot bore diameter therefore separating the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a software issue associated with the ability to properly complete a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity m System Recalled by Abbott Molecular, Inc. Due to There is a...
The Issue: There is a potential for abnormal (non-sigmoidal) amplification curves.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic HawkOne Directional Atherectomy System Recalled by ev3 Inc. Due to...
The Issue: Reports have been received of tip damage during use of the devices which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medique Pain-Off (Acetaminophen 250 mg Recalled by Medique Products Due to...
The Issue: CGMP Deviations: manufacturer recalled after an FDA inspection noted that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mitomycin-C Sterile Ophthalmic Solution Recalled by Edge Pharma, LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.