Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
ðĶī
Implants & Prosthetics
ðĨ Medical Devices âĒ 4,589 recalls
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Potentially insufficient cleaning process or potential inadequate process monitoring for cleaning parameters.
Class I - Dangerous
Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Class I - Dangerous
Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
A limited number of tibial trays were labeled with an incorrect serial number and were delivered to the wrong customer accounts.
Class I - Dangerous
Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Class I - Dangerous
Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
A limited number of tibial trays were labeled with an incorrect serial number and were delivered to the wrong customer accounts.
Class I - Dangerous
Instructions for Use (IFU) and Surgical Cleaning and Sterilization Protocols updated with revised dry time parameters. This recall of IFU occurred in 2018.
Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.
Firm has identified that the product may be at risk of incorrectly containing a tunneler with a barb tip meant to attach to a 6Fr catheter instead of the correct barb tip for a 9.6Fr catheter. This can result in a prolongation of operation.