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. 2,548 recalls have been distributed to Nebraska in the last 12 months.
Showing 14441–14460 of 28,140 recalls
Recalled Item: SmartSite Syringe Administration Set-Product Package Size 50 Recalled by...
The Issue: Leaking of the Smartsite Syringe Administration Set. May result in delay or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spine & Trauma 3D Navigation 1.0 (subpart of the system Recalled by Brainlab...
The Issue: In certain occurrences, the affected navigation software application might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TIN ABUTMENT 3.4MM Recalled by Biomet 3i, LLC Due to...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: Recalled by...
The Issue: The safety interlock covering the septum piercing probes within the bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Alinity c Processing Module LN 03R67-01 - Product Usage: Recalled by...
The Issue: The safety interlock covering the septum piercing probes within the bulk...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CERTAIN(R) BELLATEK(R) TITANIUM ABUTMENT 3.4MM Recalled by Biomet 3i, LLC...
The Issue: During manufacturing, the screw stop ledge was not made to specification and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral Vein Approach Recalled by...
The Issue: Updates to the Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Femoral and Jugular Vein...
The Issue: Updates to the Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Jugular Vein Approach Recalled...
The Issue: Updates to the Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gunther Tulip Vena Cava Filter Set for Femoral and Jugular Vein Approach...
The Issue: Updates to the Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cook Celect Platinum Vena Cava Filter Set for Femoral Vein Approach Recalled...
The Issue: Updates to the Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gunther Tulip Vena Cava Filter Set for Jugular Vein Approach Recalled by...
The Issue: Updates to the Instructions for Use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIDEK Specular Microscope Recalled by Nidek, Inc. Due to The electromagnetic...
The Issue: The electromagnetic noise exceeded the upper limit of the Electromagnetic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integrated ECG cable with 3-lead leadwires labeled as the following:...
The Issue: The Integrated ECG cable with 3-lead leadwires can short circuit during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SetSource ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical ChemoClave Vented Vial Spike Recalled by ICU Medical, Inc. Due to...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: icumedical Oncology Kit w/12" (30cm) Ext Set w/Spiros w/Red Cap Recalled by...
The Issue: There is a potential for certain lots of ChemoLock and ChemoClave Vial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.