RecallDepth

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

Company
Spineart Sa Chemin Du Pre-Fleuri 3 Plan-Les-Ouates Switzerland
Recall Initiated
June 30, 2025
Posted
August 8, 2025
Recall Number
Z-2279-2025
Quantity
16 units

Reason for Recall

Cannulated fenestrated polyaxial screws may be incorrectly labeled

Distribution

US Nationwide distribution in the states of Florida , Kentucky, California.

Lot / Code Info

Lot Code: Lot number 8-4528 GTIN 07640305160561

Root Cause

Labeling Change Control

Action Taken

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 orders@spineart.us (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.

More recalls by Spineart Sa Chemin Du Pre-Fleuri 3 Plan-Les-Ouates Switzerland

View all recalls by this company →