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Articles published by Fresenius Kabi
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Fresenius Kabi Issues Nationwide Recall of Tyenne® (tocilizumab-aazg) Injection 400 mg/20 mL Vials Due to Presence of Glass Particles
August 10, 2026
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Issues Voluntary Nationwide Recall of One Lot of Morphine Sulfate Injection, USP in a Simplist® Prefilled Syringe Due to Labeling Mix-up
August 04, 2026
From
Fresenius Kabi
Via
Business Wire
Fresenius Announces FDA Approval of Rituximab Biosimilar for the U.S. Market
August 03, 2026
From
Fresenius Kabi
Via
Business Wire
Fresenius Announces FDA and EMA Acceptance for Review of Vedolizumab Biosimilar Candidate
July 31, 2026
From
Fresenius Kabi
Via
Business Wire
CMS Grants Fresenius Kabi COVID-19 Indication-Specific HCPCS Codes for Tyenne® (tocilizumab-aazg)
April 09, 2026
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Recognized as a Top Employer in the United States for the Fourth Consecutive Year
January 20, 2026
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi, TQ Therapeutics Announce Cell Therapy Technology Agreement
January 14, 2026
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Introduces New Presentation of Otulfi® (ustekinumab-aauz), a Biosimilar to Stelara®
January 06, 2026
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Introduces First-Ever Rocuronium Bromide Injection Stable at Room Temperature
December 18, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Expands Operating Room Portfolio with New Simplist® Prefilled Syringes
December 02, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Introduces Dalbavancin for Injection (for single-dose regimen use only)
November 24, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi’s Adaptive Nomogram used on Aurora Xi Plasmapheresis System Now Operating Nationwide at BioLife Plasma Centers
November 12, 2025
From
Fresenius Kabi
Via
Business Wire
CORRECTING and REPLACING Fresenius Kabi Issues Voluntary Nationwide Recall of Three Lots of Famotidine Injection, USP, 20 mg per 2 mL (10 mg per mL), 2 mL Fill in a 2 mL Vial Due to Out-of-Specification Endotoxin Results in Certain Reserve Samples
November 12, 2025
From
Fresenius Kabi
Via
Business Wire
FDA Grants Interchangeable Designation to Fresenius Kabi’s Biosimilars Conexxence® and Bomyntra® (denosumab-bnht)
October 29, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Announces 13 New Inductees Into the National Blood Donation Hall of Fame
October 22, 2025
From
Fresenius Kabi
Via
Business Wire
CMS Grants Fresenius Kabi Permanent, Product-Specific Q-Code for Conexxence® and Bomyntra® (denosumab-bnht)
September 29, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Receives Two Major Awards for Supply and Service Excellence from Vizient®
September 25, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi and AABB Announce 20th Anniversary of Blood Collectors Week, September 7–14, 2025, Honoring Lifesaving Blood Collection Professionals
September 07, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Leads New EASYGEN Consortium Aimed at Decentralizing CAR-T Cell Therapy and Improving Hospital Workflows
August 26, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Receives 2025 Premier Supplier Legacy Award
July 17, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Expands Biosimilars Portfolio With The Launch of Denosumab Biosimilars in the U.S.
July 01, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Introduces Epinephrine Injection, USP, in 30 mg per 30 mL Multi-Dose Vials
May 20, 2025
From
Fresenius Kabi
Via
Business Wire
FDA Grants Interchangeable Designation to Fresenius Kabi’s biosimilar Otulfi® (ustekinumab-aauz)
May 19, 2025
From
Fresenius Kabi
Via
Business Wire
CMS Grants Fresenius Kabi Permanent, Product-Specific Q-Code for Otulfi® (ustekinumab-aauz)
April 28, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Receives FDA Approval for their Denosumab Biosimilars and Secures Global Settlement Agreement
March 27, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Continues Growth of Biosimilars Portfolio with the U.S. Availability of Otulfi® (ustekinumab-aauz)
March 03, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Introduces Calcitonin Salmon Injection, USP Synthetic
February 10, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Receives FDA 510(k) Clearance for Adaptive Nomogram, Enhancing Plasma Collection Efficiency with the Aurora Xi Plasmapheresis System
January 28, 2025
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Launches Epinephrine Injection, USP Expanding U.S. Pharma Portfolio
December 17, 2024
From
Fresenius Kabi
Via
Business Wire
Fresenius Kabi Submits 510(k) Notification for the Aurora Xi Plasmapheresis System Software Version 2.0 with New Nomogram
November 21, 2024
From
Fresenius Kabi
Via
Business Wire
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