95,114 total recalls in our database
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Failed Dissolution Specifications: Low out of specification dissolution result observed during stability testing.
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
Fusion IV Pharmaceuticals, Inc.
Lack of Assurance of Sterility
1)Error 255-XX-XXX results in inability to edit settings 2)Delay options programming may result in no KVO rate/therapy interruption 3)Software errors results in no low battery alarm/infusion stopping 4)Medium priority KVO/End of Infusion alarms may result in unrecognized infusion completion 5)Custom concentration data entry errors results in concentrations being lower/higher than medication orders
Normand-Info S.A.S.U.
A patch was released for a critical remote code execution vulnerability in remote desktop services. This vulnerability can be exploited remotely without authentication on certain operating systems. An attacker who successfully exploited this vulnerability could execute arbitrary code on the target system; then install programs; view, change, or delete data; or create new accounts with full user rights. If the vulnerability could be exploited locally, it would lock down the computer.
It has been determined that some units of catheters were not tightly connected to the thumb port. This may result in the catheter disconnecting from the thumb port which could reduce the suction performance and make it difficult to remove from the patient's trachea.
Bard Peripheral Vascular
Lot numbers and products inadvertently not included in the scope of the previous recall. Original recall was conducted due to an increase in probe failures for leaks, suction issues, and failure to obtain samples.
Insufficient shielding of Philips SensaVue DVI Adapter for computer monitor.
Sterile packaging may potentially be compromised, and use of products may result in increased risk for infection.