Fresenius Kabi USA IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet recall — FDA Z-0586-2026
Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury.
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury.
Potential issue where the IntelliVue monitors did not alarm.
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for…
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
There were instances where the operator table was sold together with a bus-installation kit. The operator table is not intended and not released for bus installations as it was designed for…
Potential issue where the IntelliVue monitors did not alarm.
Fibula nail system intended for use in fixation of fibular fractures and osteotomies, has out of specification thread depths on the fibula nail, so implant may not be able to mate properly…
Potential issue where the IntelliVue monitors did not alarm.
If the screws of tube heat exchanger on the rotating scanner are not tightened well after replacing. This component may become detached and make contact with other components located within…
Potential issue where the IntelliVue monitors did not alarm.
Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set.
Replacement bladder kit for the Welch Allyn two-piece reusable blood pressure cuff may contain a Large Adult size bladder rather than a Thigh size bladder in the replacement kits.
Ultrasound system compatibility issues with Apple devices running iOS 18 may cause a failure to perform live imagining.
Potential issue where the IntelliVue monitors did not alarm.
Potential issue where the IntelliVue monitors did not alarm.
Potential issue where the IntelliVue monitors did not alarm.
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2025 Tiguan vehicles. The passenger occupant detection system (PODS) may experience a fault in the wiring and deactivate…
Potential metal fragments from supplier raw material (downstream recall)
The 3oz. sealed packet of Caesar Dressing in Costco Caesar Salad may contain plastic material.
Potential metal fragments from supplier raw material (downstream recall)
Product tested positive for Salmonella.
Potential metal fragments from supplier raw material (downstream recall)
Half-pint chocolate fat free milk is recalled due to potential quality control issues.
Products do not declare milk in the Contains statement or the ingredient statement.
Browse recent months with enough recall history for useful comparison.