Product Recalls in Nebraska
Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,439 recalls have been distributed to Nebraska in the last 12 months.
Showing 27621–27640 of 28,140 recalls
Recalled Item: X-COATED H/L PK W/FX15RW40 Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM CPB CATHETER KIT-DR. The Sarns High Flow Aortic Arch Recalled by...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT- DR HENDRICKSO Product Usage: The Sarns Cardioplegia...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien ROTICULATOR 30-4.8 Single Use Stapler REF# 017617 The RETICULA...
The Issue: Potential for the sterility barrier to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED SMALL PATIENT PACK Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-COATED FX25RW H/L PACK Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien ROTICULATOR 30-3.5 Single Use Stapler REF# 017615 The RETICULA...
The Issue: Potential for the sterility barrier to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT- DR OWEN Product Usage: The Sarns Cardioplegia Recalled by...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPB CATHETER KIT-DR BARTLES Product Usage: The Sarns Cardioplegia Cannula...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SARNS ANTEGRADE: CARDIOPLEGIA CANNULA: ROOT INFUSION VENT/CATHETER WITH 14-...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPECIALTYCARE - HUDGENS. The Sarns High Flow Aortic Arch Cannula Recalled by...
The Issue: During production of one lot of the Sarns High-Flow Aortic Arch Cannula,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sarns Antegrade Cardioplegia Cannula: ROOT INFUSTION VENT CATHETER WITH 12...
The Issue: During production of the Sarns Antegrade Cardioplegia Cannula, Terumo...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12...
The Issue: Siemens Healthcare Diagnostics has confirmed that the presence of Intrinsic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeautyAngel Health Fitness Natural Collagen Stimulation Anti Aging For human...
The Issue: The Beauty Angel was marketed without a 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: USA-002 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: US-001 Rev A brochure is a two sided tri-fold printed Recalled by...
The Issue: Non-Invasive Monitoring Systems Inc (NIMS) is voluntarily recalling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V Series Patient Monitors Recalled by Mindray DS USA, Inc. d.b.a. Mindray...
The Issue: Mindray has identified two software anomalies contained in the V Series...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lynx TM20 Torquemaster Low Speed Handpiece MTI Dental Products Recalled by...
The Issue: Sharp edge on the body/housing of the Lynx TM20 TorqueMaster Low Speed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Scenaria CT System Software Product Usage: The Scenaria system...
The Issue: Hitachi discovered a software error in the Reconstruction Status function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Depuy Spine Side Fire Needles 13G X 6IN Recalled by DePuy Mitek, Inc., a...
The Issue: Additional Instructions for Use and Surgical Technique for the Confidence...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.