All Recalls

95,025 total recalls in our database

Prismaflex Control Unit

Baxter Healthcare

🏥 Medical Devices Class I - Dangerous

Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed.

Apr 7, 2020 Other Medical Devices View Details →

May exhibit increased levels of artifacts which could be difficult to distinguish from gram positive cocci, increased levels of artifacts could result in a false-positive Gram stain

Apr 14, 2020 Infusion Pumps Nationwide View Details →

There is a remote potential for the sterile packaging of the transseptal guiding sheath to be compromised during shipping and handling. In the case that a packaging defect is not identified and the product is used in a patient, there may be a remote risk of infection.

Oct 7, 2019 Other Medical Devices View Details →

The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two pieces welded together which has been associated with the spreader tip breaking off during the procedure.

Apr 13, 2020 Implants & Prosthetics Nationwide View Details →

The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two pieces welded together which has been associated with the spreader tip breaking off during the procedure.

Apr 13, 2020 Implants & Prosthetics Nationwide View Details →

Possible mis-labeling of the device with incorrect serial number labels which may result in a patient's misdiagnosis.

Jul 3, 2019 Diagnostic Equipment Nationwide View Details →

The Aleutian Anatomically Narrow Lordotic Spreader was manufactured as two pieces welded together which has been associated with the spreader tip breaking off during the procedure.

Apr 13, 2020 Implants & Prosthetics Nationwide View Details →

Damaged ESD bags used for storing components in Processor PCA Replacement Kits

Apr 10, 2020 Diagnostic Equipment Nationwide View Details →