EP Healing Abutment Dental implants
Biomet 3i
Pouches may not have been sealed during packing.
ðĨ Medical Devices âĒ 4,540 recalls
Biomet 3i
Pouches may not have been sealed during packing.
TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.
Pouches may not have been sealed during packing.
Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck).
Medtronic Cardiovascular Surgery-the Heart Valve Division
Potential for vascular trauma with the use of the Medtronic EnVeo R Delivery Catheter System (DCS).
TRYX products are being recalled since the processes of spaying, welding, drying oven and polymer were not adequately validated.
Biomet 3i
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.
Biomet 3i
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.
Pouches may not have been sealed during packing.