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. 2,455 recalls have been distributed to Nebraska in the last 12 months.
Showing 22861–22880 of 28,140 recalls
Recalled Item: The MAYFIELD¿ Ultra 360 Base Unit for head positioner Recalled by Integra...
The Issue: Through an investigation of complaints, Integra found that there is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: lnline Persuader- PedFuse Pedicle Screw System Recalled by SpineFrontier,...
The Issue: A crack may develop in the handle to the Inline Persuader, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINAC Accelerators: ARTISTE Recalled by Siemens Medical Solutions USA, Inc...
The Issue: A hardware update to replace the old PCB Assembly, Head Driver-G41 with PCB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Information Center iX (release A.00 Recalled by Philips...
The Issue: Sp02 and/or Non Invasive Blood Pressure (NBP) alarms may become disabled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The XN-Series modules (XN-10 Recalled by Sysmex Corporation Due to There is...
The Issue: There is a potential for elevated hemoglobin (Hgb) and impedance platelet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas b 221 (versions 5 and 6) Blood Gas and Electrolytes Analyzer Recalled...
The Issue: Chemical component of the F3 Fluid pack and environmental bacterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ti-Bond Marketing Literature/Labeling Recalled by Spinal Elements, Inc Due...
The Issue: Spinal Elements is recalling the Ti-Bond related brochures that includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform...
The Issue: The devices were not shipped with the Starter Kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merlin@home RF Remote Monitoring Transmitter Recalled by St Jude Medical...
The Issue: Transmitter may initiate a software reset resulting in backup operation in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block...
The Issue: Potential for implant deformation, implant mechanical stability too low,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Femoral Head - indicated for hip arthroplasty for noncemented Recalled...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants...
The Issue: Potential for implant deformation, implant mechanical stability too low,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul Femoral Head - A modular head component is used Recalled by Zimmer...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul Femoral Head - indicated for total hip arthroplasty for Recalled by...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biolox Delta Femoral Head - The BIOLOX delta Ceramic Femoral Recalled by...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Femoral Head - A modular head component is used Recalled by Zimmer Gmbh...
The Issue: Potential compromise of the inner sterile tray. If a compromised tray is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Miethke Shunt System accessories Product Usage: - The Miethke Shunt Recalled...
The Issue: Some Miethke Shunt System accessories may have an incorrect MR safety symbol...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR TITAN MAX Orbital Floor and Wall (OFW) MEDPOR-Titanium-Barrier (MTB)...
The Issue: Article #81036 (MEDPOR Titan Max OFW - MTB - Right) reportedly contained...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm Recalled by Stryker...
The Issue: Potential for implant damage, implant cracking off/breaking intra-operatively.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liquid Mouse Monoclonal Antibody CD15 used is laboratories to perform...
The Issue: The staining intensity decreases over the shelf life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.