Preat Corp: Medical Device Recall in 2024 - (Recall #: Z-2318-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

9006767 Astra EV 4.8mm Milled Titanium Abutment Milled abutments are too be used in conjunction with an endosseous dental implant fixture to aid in prosthetic rehabilitation.

Product Classification:

Class II

Date Initiated: April 10, 2024

Date Posted: July 17, 2024

Recall Number: Z-2318-2024

Event ID: 94693

Reason for Recall:

Due to incorrect milled titanium abutment being packaged and labeled.

Status: Ongoing

Product Quantity: 7 abutmens

Code Information:

Model Number: 9006767 UDI-DI code: 00842092159477 Lot Numbers: ED11-20247825, ED11-20248895, ED11-20249165 and 241588

Distribution Pattern:

U.S.: CA, MO, and NV. O.U.S.: None

Voluntary or Mandated:

Voluntary: Firm initiated