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. 1,095 recalls have been distributed to Nevada in the last 12 months.
Showing 6261–6280 of 28,334 recalls
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Probe Cover Kits containing sterile Ultrasound Gel Recalled by...
The Issue: Probe covers for use during diagnostic ultrasound procedures may have an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-iD Adult Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX-i Adult Recalled by Maquet Medical Systems USA Due to Product...
The Issue: Product packaging may exhibit small pinholes which may not be visible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUADROX -i Neonatal Recalled by Maquet Medical Systems USA Due to 1. An...
The Issue: 1. An accessory may be improperly placed during packaging, causing creases...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Ventricular Assist Device System. a) Monitor 1521US Explore Tech...
The Issue: Medtronic has identified that the logfiles downloaded from the recently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Draeger Softbed Resuscitaire and/or Birthing Room Warmer with Scale...
The Issue: The Resuscitaire Infant Radiant Warmer with the optional scale could display...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Storage and Retrieval Module (SRM) Recalled by Siemens...
The Issue: A firmware error may lead to an incorrect association of test result(s) to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris Balloon Dilation Catheter Recalled by Bryan Medical Inc Due to Mislabeling
The Issue: Devices were mislabeled.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of...
The Issue: Potential for lot number discrepancies between the test strip packaging and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite Systems with 9-inch Image Intensifier Recalled by GE OEC Medical...
The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...
The Issue: Potential for the labeled sterile ultrasound gel component within packs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.