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. 2,722 recalls have been distributed to Nevada in the last 12 months.
Showing 1161–1180 of 28,334 recalls
Recalled Item: Artis Pheno. Image-Intensified Flouroscopic X-Ray System. Recalled by...
The Issue: Limited system movements after startup .
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: FLEX Monoclonal Mouse Anti-Human CD20cy Recalled by Agilent...
The Issue: Their is the potential for weak staining which may result in false negative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP). Material Number:...
The Issue: Potential for falsely depressed patient, quality control (QC), and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to Merge Healthcare has...
The Issue: Merge Healthcare has been informed by Schiller AG (Baar, Switzerland) of an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Greiner BIO-ONE VACUETTE 2 ml 9NC Coagulation sodium citrate 3.2% Recalled...
The Issue: Blood collection tubes were manufactured with the label applied too high on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argus PB-3000 Recalled by Schiller, Ag Due to Vital sign monitoring...
The Issue: Vital sign monitoring instrument may trigger an error message during blood...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...
The Issue: Software issue that results in the display of outdated information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 8B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 11A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 10B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 12A...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 7 Recalled...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation with the following product descriptions: 1. RayStation 2023B...
The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...
The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.