Limacorporate S.p.A: Device Recall

Recall #Z-2025-2025 · 05/19/2025

Class II: Risk

Recall Details

Recall Number: Z-2025-2025
Classification: Class II
Product Type: Device
Recalling Firm: Limacorporate S.p.A
Status: Ongoing
Date Initiated: 05/19/2025
Location: San Daniele Del Friuli, Italy
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 9 units

Reason for Recall

There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.

Product Description

PRIMA 4MM ECCENTRICAL ADAPTOR WITH SCREW, REF:1367.15.704, Sterile

Distribution Pattern

Worldwide - US Nationwide distribution in the states of VA, FL, SC, MS, NY, TX and the countries of Italy, Poland, France.

Other Recalls by Limacorporate S.p.A

Class II: Risk 05/19/2025

There is the potential that the eccentrical adaptor with screw, black laser marking, use to identify the position may be missing.
Class II: Risk 10/02/2024

Due to a potential difference in mechanical behavior between the implanted device and tool(s) used during revision surgery.

View all recalls by Limacorporate S.p.A →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.