EndoWrist Suction Irrigator, Single Use Instrument. Part Number: 480299-04. An accessory to the EndoWrist Surgical System, used in endoscopic surgery.
FDA Recall Z-0249-2020 · Posted None
Recalling FirmIntuitive Surgical, Inc.
Recall StatusOpen, Classified
Product CodeNAY
Date Initiated2018-06-04
Product Quantity3108 units (518 boxes of 6 units)
Reason for Recall
The firm has identified the potential for a silicone particle to be generated within the Suction Irrigator device. If generated, a particle may be introduced into the patient with irrigation.
Firm Action
On 06/04/2018, Medical Device Recall notices (Field Safety Notice Urgent Medical Device Correction- ISIFA2018-09-C) were emailed to U.S. consignees, and on 06/07/2018 notices were mailed via FedEx. Additionally on 06/08/2018 two (2) distributors received the notices via email and on 06/15/2018 two (2) EMEIA consignees received the notices by mail. The firm posted information regarding the voluntary field recall on their US Customer Portal on 06/04/2018. Customers were asked to:
1. Stop-use of the affected products for intra-cardiac procedures until further notice from the Recalling Firm.
2. Ensure surgeons and patient side assistants using the products have read and understand the content of the notification letter.
3. Complete the attached Acknowledgement Form and return it via fax or email to U.S. FAX +1(408)523-0619, or Scan and Email [email protected] or for further questions contact Customer Service at:
-North and South America: 800-876-1310 Option 3 (4 am to 5 pm PST)
-Europe, Middle East, Asia and Africa: +800 0821 2020 or +41 21 821 2020 (8 am to 6 pm CET)
4. Please retain a copy of the Customer Notification and the Acknowledgement form on file.
Root Cause
Process change control
Distribution Pattern
Worldwide distribution. US nationwide, Australia, Italy, Switzerland, and United Kingdom.
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.