Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K
Keystone Dental
Class I - Dangerous
Straight PrimaConnex Implants contained Tapered PrimaConnex Implants
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Implants & Prosthetics
ðĨ Medical Devices âĒ 4,540 recalls
Incorrect valve rotor orientation due to misalignment and/or off-center positioning of the StrataMR Locator Tool: When the StrataMR valve is set in the incorrect orientation, higher valve opening pressures result leading to a corresponding underdrainage in CSF fluid performance. This condition may result in the following adverse health consequences: ventriculomegaly, headaches, nausea, vomiting and lethargy. If left untreated, underdrainage has the potential to lead to coma and death.
Class I - Dangerous
A single lot of product that potentially has a single part within the lot that does not match the product on the label due to a commingle at the firm supplier
Regard, Item Number: 800550001, Sterile, OR0639A - Hip Shoulder - Medical Center Santa Rosa
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 880328002, Sterile, HT0759B - Pacemaker Pk - OSU
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 880328001, Sterile, HT0759A - Pacemaker Pk - OSU
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 800414003, Sterile, OR0483C - Total Joint Pk - Spohn
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 800414002, Sterile, OR0483B- Total Joint Pk - Spohn
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Class I - Dangerous
The locking lever pin component of the femoral driver may become deformed and break, resulting in malfunction during surgery and causing the device to become inoperable.
Regard, Item Number: 800553001, Sterile, OR0642A - Total Knee - Medical Center Santa Rosa
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 800553003, Sterile, OR0642C - Total Knee - Medical Center Santa Rosa
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 880330004, Sterile, OR0761D - Total Hip - OSU
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 880331002, Sterile, OR0762B - Total Knee - OSU
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 800527003 Sterile, OR0611C - Hip Shoulder PK - Westover Hills
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 800553002, Sterile, OR0642B - Total Knee - Medical Center Santa Rosa
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 800550002, Sterile, OR0639B - Hip Shoulder - Medical Center Santa Rosa
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 880330005, Sterile, OR0761E - Total Hip - OSU
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 880330003, Sterile, OR0761C - Total Hip - OSU
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 800527004 Sterile, OR0611D - Hip Shoulder PK - Westover Hills
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.
Regard, Item Number: 880331001, Sterile, OR0762A - Total Knee - OSU
Resource Optimization & Innovation
Class I - Dangerous
Custom procedure trays contain a component, a light glove, that has been recalled by the manufacturer because it can split during application to a light handle breaking the sterile field.