FDA Recall Open, Classified

impression coping, repositionable, short, screw-retained, PF 4.0

Recall: Z-1322-2024 · Initiated January 24, 2024

Recall

Recall Number
Z-1322-2024
Event Number
94040
Firm
Thommen Medical AG Eschenweg 3 Bettlach Switzerland
FEI Number
3003184527
Product Code
NDP
Status
Open, Classified
Root Cause
Process change control
Initiated
January 24, 2024
Posted
March 20, 2024

Description

impression coping, repositionable, short, screw-retained, PF 4.0

Reason

The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.

Action

Urgent Field Safety Notice letters dated February 05, 2024 were sent to customers. Customers were instructed to: Ensure that the contents of this Field Safety Notice are read and understood within your organization. Locate and quarantine affected devices immediately. If you have further distributed the product to other organizations, please inform them at once of this FSCA and provide them with a copy of this letter. Return all affected products of the listed lot number to Thommen Medical AG. The products will be replaced by Thommen MedicalAG. Please acknowledge and confirm receipt of this urgent safety information using the enclosed reply form and return it to us together with the retrieved devices. For further questions please contact: Bibiana Gamper Phone: +41 61 965 90 55 E-Mail [email protected].

Distribution

US Nationwide distribution in the states of OH and KY.

Quantity

20 units