impression coping, repositionable, short, screw-retained, PF 4.0
FDA Recall Z-1322-2024 · Posted 2024-03-20
Recalling FirmThommen Medical AG
Recall StatusOpen, Classified
Product CodeNDP
Date Initiated2024-01-24
Product Quantity20 units
Reason for Recall
The depth of the internal canal was not manufactured according to specifications. Thus, the impression coping cannot be firmly connected to the implant.
Firm 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].
Root Cause
Process change control
Distribution Pattern
US Nationwide distribution in the states of OH and KY.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.