Preat Corp Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967
Brand
Preat Corp
Lot Codes / Batch Numbers
Model Number: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489
Products Sold
Model Number: 9000967 UDI-DI code: 00842092165867 Lot Numbers: 235650, 234294, 233667, 233885, 233439, and 231489
Preat Corp is recalling Preat Nobel Active/Conical-compatible RP Titanium Blank, REF 9000967 due to 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 lengt. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026