Brand Name: PERLA TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S Software Version: Not Applicable Product Description: CANNULATED FENESTRATED POLYAXIAL SCREW Component: No
FDA Recall Z-2279-2025 · Posted 2025-08-08
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Recalling FirmSPINEART SA
Recall StatusOpen, Classified
Product CodeNKB
Date Initiated2025-06-30
Product Quantity16 units
Reason for Recall
Cannulated fenestrated polyaxial screws may be incorrectly labeled
Firm Action
On July 4, 2025, Spineart SA, issued a Urgent: Medical Device Recall Notification to affected consignees via E-Mail. On July 10, 2025, Spineart SA issued a revised notification to provide additional information. On July 16,2025, Spineart expanded the recall to include an additional product and lot. Spineart SA ask consignees to take the following steps:
(1) Please acknowledge receipt of this letter by emailing to [email protected]
(2) Please discontinue use and return any product on hand that is listed in the Product and Distribution Information section of this letter to:
Spineart U.S.A.
23332 Mill Creek Drive Suite 150
Laguna Hills, CA. 92653
(3) You may have further distributed this product; please identify concerned customers and notify them at once of this product recall by using this document.
(4) Surgeons/physicians should closely monitor patients that have been implanted with these potential non-conforming screws.
Root Cause
Labeling Change Control
Distribution Pattern
US Nationwide distribution in the states of Florida , Kentucky, California.
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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