RecallDepth

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

Company
Preat Corp
Recall Initiated
February 9, 2024
Posted
March 20, 2024
Recall Number
Z-1321-2024
Quantity
561 units
Firm Location
Santa Maria, CA

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.

Lot / Code Info

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

Root Cause

Process change control

Action Taken

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 nfetterman@younginnovations.com 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.

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