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. 2,076 recalls have been distributed to Nevada in the last 12 months.
Showing 3741–3760 of 50,223 recalls
Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc NXS Host Recalled by Siemens Healthcare Diagnostics, Inc. Due to...
The Issue: Siemens Healthcare Diagnostics is recalling their epoc Blood Analysis System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Javygtor (sapropterin dihydrochloride) Tablets 100mg Recalled by Dr. Reddy's...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dihydroergotamine Mesylate Injection Recalled by Provepharm Inc. Due to...
The Issue: Discoloration
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VCF Recalled by Apothecus Pharmaceutical Corp. Due to CGMP deviations: out...
The Issue: CGMP deviations: out of specifications for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Kit for the Preparation of Technetium Tc 99m Sulfur Colloid Injection...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: OEC 9800 Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: See DocMan Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Custom...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 3D Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc Due...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) CERVICAL PACK-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite Fluoroscopic X-Ray System Recalled by GE OEC Medical Systems, Inc...
The Issue: Due to manufacturing issue of insufficient sealing of X-ray tubes and can...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) UMC DR. BAKER...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) ENSEMBLE RACHIS-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SynchroMed II Model 8637 and SynchroMed III Model 8667 implantable Recalled...
The Issue: Software issues were identified in application version 2.x.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline custom medical procedure kits labeled as: 1) NEURO BASIN PACK-LF...
The Issue: Custom convenience kits are being recall because the contain non-sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.