Preat Corp: Medical Device Recall in 2023 - (Recall #: Z-0152-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Preat REF 9007121, Neodent GM x 2mm Healing Abutment, Rx Only, Non-Sterile, Single Use Only. Dental

Product Classification:

Class II

Date Initiated: July 18, 2023

Date Posted: November 1, 2023

Recall Number: Z-0152-2024

Event ID: 92867

Reason for Recall:

The healing abutments contain a dimensional condition that may lead to a gap between the healing abutment and the implant allowing for microleakage

Status: Ongoing

Product Quantity: 13 units

Code Information:

UDI-DI: 00842092161364/Lot # OF018356

Distribution Pattern:

US: FL, CA, OR, TX, OH, CA, SC, OR, NJ, SC, OUS: None

Voluntary or Mandated:

Voluntary: Firm initiated