NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation platform used to perform a reverse shoulder arthroplasty on the glenoid
FDA Recall Z-0372-2023 · Posted 2022-12-03
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Recalling FirmMedacta Usa Inc
Recall StatusTerminated
Product CodeOLO
Date Initiated2022-10-27
Date Terminated2023-10-23
Product Quantity14 units
Reason for Recall
A warning has been added to the Surgical Technique for NextAR Shoulder, advising verification of suitable patient conditions prior to placement of the NextAR Shoulder Target Holder:
WARNING
Target fixation requires adequate coracoid bone stability. Osteoporosis, weakness of the coracoid process, or other deficiencies, could lead to adverse events including bone fracture. Verify that the coracoid bone and relevant patient conditions are suitable before proceeding.
Firm Action
Medacta issued an URGENT - Field Safety Notice to the surgeons on 10/28/2022 by email The notice provided the following information:
"1. Description of advisory:
The following Warning has been added to the Surgical Technique for NextAR Shoulder, advising verification of suitable patient conditions prior to placement of the NextAR Shoulder Target Holder:
WARNING
Target fixation requires adequate coracoid bone stability. Osteoporosis, weakness of the
coracoid process, or other deficiencies, could lead to adverse events including bone fracture. Verify that the coracoid bone and relevant patient conditions are suitable before proceeding.
The updated Surgical Technique is attached to this document and can be found at: resources.medacta.com.
2. Action to take:
- Transmit this communication all end-users, ensuring it is fully understood.
- Verify acknowledgment through end-user signature on the attached receipt.
- Return all the signed receipts to the Regulatory Department of Medacta International.
3. Contact person and return address:
Stefano Baj, Regulatory Affairs Director
Medacta International SA, Strada Regina, CH-6847 Castel San Pietro, Switzerland
Tel: +41 (0)91 696 60 60, Fax: +41 (0)91 696 60 66"
Root Cause
Other
Distribution Pattern
AL, FL, NH, CO, IL, SC, AR
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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