FDA Recall Open, Classified

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

Recall: Z-1321-2024 · Initiated February 9, 2024

Recall

Recall Number
Z-1321-2024
Event Number
94032
Firm
Preat Corp
FEI Number
2918719
Product Code
NHA
Status
Open, Classified
Root Cause
Process change control
Initiated
February 9, 2024
Posted
March 20, 2024
Address
2625 Skyway Dr, Ste B, Santa Maria, CA, 93455-1405

Description

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

Reason

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.

Action

On 02/09/2024, the firm sent an "URGENT: MEDICAL DEVICE RECALL" Letter via US certified mail to customers to inform them that the abutment was manufactured with a dimensional condition that may lead to reduced engagement between the prosthetic screw and the implant. Customer are instructed to inspect their inventory and discard or return the affected products to PREAT CORPORATION. For questions or further assistance contact the Quality Assurance Manager at 800-232-7732 or email at [email protected] On 2/16/2024, the firm sent via certified USPS mail an "URGENT: MEDICAL DEVICE RECALL UPDATE" which informs customer to notify all personnel within their company, and of their customers where the affected products may have been further distributed of the recall.

Distribution

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

Quantity

561 units