Preat Corp: Medical Device Recall in 2024 - (Recall #: Z-1321-2024)

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:

Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967

Product Classification:

Class II

Date Initiated: February 9, 2024

Date Posted: March 27, 2024

Recall Number: Z-1321-2024

Event ID: 94032

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.

Status: Ongoing

Product Quantity: 561 units

Code Information:

Model Number: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated