Class 2 Device Recall Integra

• Date Initiated by Firm: May 29, 2024
• Date Posted: June 21, 2024
• Recall Status: Open, Classified
• Recall Number: Z-2167-2024
• Recall Event ID: 94724
• 510(K)Number: K141674
• Product Classification: Instrument, ultrasonic surgical - Product Code LFL
• Product: CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical procedures where fragmentation, emulsification and aspiration of soft and hard tissue Catalog Number: C2600* *Note: you may see C2600P or C2600SRL on labeling. This notice is applicable for those SKUs as well
• Code Information: UDI-DI: 10381780039419 All serial numbers distributed before 12/14/2023 Product manufactured before 11/01/2023. SN: Handpiece manufactured Prior to HAL23XXXXXXIE (represents a product that is manufactured in November 2023): HA indicating the product family Letter indicating the month of manufacture where A = January; B = February, L=November. Two digits e.g 23 indicating the year of manufacture with 23 representing 2023
• Recalling Firm/ Manufacturer: Integra LifeSciences Corp.; 1100 Campus Rd; Princeton NJ 08540-6650
• For Additional Information Contact: Lacey Gigante ; 609-212-9004
• Manufacturer Reason for Recall: Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may result in delay of treatment
• FDA Determined Cause: Process design
• Action: Integra issued First Notification- Urgent: Voluntary Medical Device Correction on via courier service, facsimile or email about the initial notification between May 29, 2024 and May 31, 2024. Letter states reason for recall, health risk and action to take: B. If your handpiece was manufactured prior to HAL23XXXXXXIE you should take the following actions 1. Inspect the housing for the presence of a crack 2. The Handpiece cracked housing may be visually detected by clinical staff during inspections prior to or postsurgery. If a crack is noted, please remove the handpiece, contact Integra Service and Repair to obtain a Return Material Authorization (RMA), and return to Integra Service and Repair (S&R) for a free housing replacement. The contact information for US S&R is: Integra " 4900 Charlemar Drive, Dock B, Cincinnati, Ohio 45227, Phone Number: 877-444-1114 Option 2, email: integra-service@integralife.com 3. If a crack is not noted, a. Regardless of the service contract status, the housing will be replaced free of charge during your next service. b. **Please note that as per our standard IFU the recommended service frequency should be performed every 50 hours of use or 100 procedures whichever comes first**. 4. Complete the Acknowledgement Form and return to FCA1@integralife.com or FAX to 1-609-750-4220. 5. Keep a copy of the form for your records. Should you have any questions regarding these instructions, please contact Service and Repair: USA: 877-444-1114 Option 2, email: integra-service@integralife.com
• Quantity in Commerce: 2, 652 units
• Distribution: Nationwide Foreign: Argentina Australia Bangladesh Bangladesh Belgium Bolivia (Plurinational State of) Brazil Canada Chile China Costa Rica Dominican Republic (the) El Salvador Hong Kong India Indonesia Japan Korea (the Republic of) Malaysia Mexico Mongolia Myanmar Nepal New Zealand Pakistan Panama Peru Philippines (the) Puerto Rico Singapore Sri Lanka Taiwan (Province of China) Thailand Viet Nam
• Total Product Life Cycle: TPLC Device Report

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.

• 510(K) Database: 510(K)s with Product Code = LFL