Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 2,101–2,112 of 2,908 recalls
Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Medical convenience kits containing Medtronic Aortic Root Cannula are being recalled due to the potential excess material in the male lures on the aortic cannula.
Medline medical procedure kits, containing Medtronic Aortic Root Cannula
Beckman Coulter has determined that device software versions V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3. have a defect due of which, when all constituent tests of a calculated result are rerun, either manually ordered by the ope…
Identified curing issues with the silicone during the needles manufacturing process.
Identified curing issues with the silicone during the needles manufacturing process.
Identified curing issues with the silicone during the needles manufacturing process.
Identified curing issues with the silicone during the needles manufacturing process.
product mix-up; Vascular stent labeled as one size but contains a different size.
product mix-up; Vascular stent labeled as one size but contains a different size.
Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU)
Single-use battery-powered blood pressure monitor, for use on neonates and infants, due to vibratory noise, may not adequately detect changes in blood pressure per specification.…