Class II

Medical Device Recall: Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

Preat Corp · February 9, 2024

Reason for Recall

Due to a manufacturing issue, the screw seat location on the abutment product may be too high, causing mating screw to have a shorter engagement length into the associated implant.

Distribution

U.S. Nationwide distribution in the states of AZ, OH and PA.

States Affected

NATIONWIDE

Quantity Affected

561 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1321-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.