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 25301–25320 of 28,140 recalls
Recalled Item: Combiset Blood Line with BVM for Hemodialysis use Catalog Number: Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Consult Diagnostics¿ Eon Calcium Reagent For In-Vitro Diagnostic Use PN:...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestream DRX-Revolution Mobile X-Ray System -- Made in U.S.A. by Recalled...
The Issue: It was discovered that Carestream received a report from a customer that 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: *** 1) Cat. 4341B Recalled by Carefusion 2200 Inc Due to Catheters included...
The Issue: Catheters included in Thoracentesis Tray and Safe-T Thoracentesis Tray -...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens RAD Fluoro Uro System (Ysio Recalled by Siemens Medical Solutions...
The Issue: When using systems operating with software versions VD10A/G during a RAD...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VerSys¿ Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys...
The Issue: Based on a review of historic packaging validations, it was determined that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-LIFT Extension Shims Extension shims are manufactured from grade 5...
The Issue: Fit variation among all lots of S-LIFT extension shims with corresponding...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Globus Medical MicroFuse Putty Recalled by Globus Medical, Inc. Due to The...
The Issue: The sterility of this product to a Sterility Assurance Level (SAL) of 10(-6)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T3F Recalled by Siemens Healthcare Diagnostics Due to Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics confirmed customer complaints regarding an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captia Syphilis-G Test Kit Product Usage: This is an enzyme Recalled by...
The Issue: Trinity Biotech recalled Trinity Biotech Captia Syphilis IgG kits due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H&H Emergency Cricothyrotomy Kit (Part No. HHECT01/ HHECTK01 Recalled by H &...
The Issue: Medical device tubing used for endotracheal airway application may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Dispersion Aortic Perfusion Cannula with Duraflo...
The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bayer brand A1CNow+ MULTI-TEST A1C SYSTEM TEST KITS (PART NUMBER...
The Issue: Test results from these lots may produce a high-bias reading (by up to 20%)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex Femoral Arterial Cannula with Duraflo Coating...
The Issue: Edwards Lifesciences is recalling two lots of Duraflo Cannulas due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Title 2 Bone Screw Remover Instrument Recalled by Zimmer, Inc. Due to...
The Issue: Possibility of the weld to the quick-connect breaking when force is applied...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dental Abutment labeled in part: "4555 Riverside Drive Palm Beach Gardens...
The Issue: Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.