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 8541–8560 of 28,334 recalls
Recalled Item: LineSider Spinal System 5.5/6.0mm Recalled by Integrity Implants Inc. Due to...
The Issue: Potential for weld separation of the Upper Tulip Head component from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G: MMT-1715 Recalled by Medtronic MiniMed Due to New or...
The Issue: New or replacement insulin pumps are not pre-programmed with basal rates or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E25Bio COVID-19 Direct Antigen Rapid Test Recalled by E25Bio, Inc. Due to...
The Issue: The Test is not authorized, cleared, or approved by FDA for clinical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6" Recalled by...
The Issue: Guidewire included with two lots of Arterial Line Kits would not fit through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NeuMoDx Flu A-B/RSV/SARS-CoV-2 Vantage Test Strip Recalled by NeuMoDx...
The Issue: A risk for product contamination was identified for the affected product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Cranial Access Kits- indicated when a craniotomy is required Recalled...
The Issue: Incorrect extended expiration dates identified on the outer box label only,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 18G X 3.5 Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5 Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATRAUMATIC ADULT LUMBAR PUNCTURE TRAY Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 20G X 3.5 DP Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS LUMBAR PUNCTURE TRAY ADULT Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000...
The Issue: Due to a component in the hemodialysis console there is the possibility of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SAFE-T PLUS ATRAUMATIC ADULT LP TRAY Recalled by Bard Peripheral Vascular...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE DRUG FREE TRAY 22G Recalled by Bard Peripheral Vascular Inc...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BenchMark ULTRA and DISCOVERY ULTRA Instruments Recalled by Ventana Medical...
The Issue: Potential for Fluid Leak inside a staining system that could cause an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PCA 4000 Curing Units Recalled by Envisiontec US Llc Due to The PCA 4000 may...
The Issue: The PCA 4000 may not fully cure EnvisionTEC dental resins to desired product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUMBAR PUNCTURE TRAY ADULT 22G X3.5 STRL Recalled by Bard Peripheral...
The Issue: Due to lumbar puncture tray manometer failure mode of leaking and mating issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Sight OLO device is a computer vision based platform Recalled by SIGHT...
The Issue: In instances where custom ranges were configured on the device post...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.