Fresenius
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News coverage of the Fresenius class action lawsuit, aggregated automatically from public reporting. Each item below is our own summary with a link to the original source — we never reproduce the source article's text.
Recent coverage
Fresenius Medical Care Renal Therapies Group Issues Recall Of 5008X HD/HDF Standard Blood Tubing Set - marketscreener.com
Fresenius Medical Care Renal Therapies Group announced a recall of its 5008X HD/HDF Standard Blood Tubing Set.
Fresenius Logged Leaking Dialysis Bags as Property Damage and Waited Eight Months Before Recalling the Affected Lots
Fresenius recalled affected dialysis bag lots after FDA inspectors identified that dozens of leakage complaints had been classified as property damage.
Fresenius Recalls 1,140 Dialysis Machines Over Alarms That Can Force Patients Onto Backup Equipment During Treatment - medicaldaily.com
Fresenius has recalled 1,140 dialysis machines because alarm problems may require patients to switch to backup equipment during treatment.
Your Reports at Work: Fresenius Kabi Morphine Recall - ECRI
ECRI reports on a recall involving Fresenius Kabi morphine products.
Infusion Pump Correction: Fresenius Kabi Issues Correction for dropped or jarred Ivenix Large Volume Infusion Pumps - fda.gov
Fresenius Kabi issued a safety correction for Ivenix large-volume infusion pumps that were dropped or jarred.
Coverage above aggregates public news reporting using the GDELT news database and Google News, updated automatically without human review. It is general information, not legal advice, and does not indicate CaseValuation.com represents or is affiliated with any party, law firm, or plaintiff named above. CaseValuation.com is not a law firm. If you believe you're affected by one of these matters, consult a licensed attorney.