Intuitive Surgical, Inc. Intuitive brand da Vinci S, 5 mm Instrument Cannula Model/Part Number: 420011-02, Product is manufactured and distributed by Intuitive Surgical , 950 Kifer Road, Sunnyvale, CA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Intuitive brand da Vinci S, 5 mm Instrument Cannula Model/Part Number: 420011-02, Product is manufactured and distributed by Intuitive Surgical , 950 Kifer Road, Sunnyvale, CA
Brand
Intuitive Surgical, Inc.
Lot Codes / Batch Numbers
Lot Numbers Affected: SA070902, SA071101, and SA071401
Products Sold
Lot Numbers Affected: SA070902, SA071101, and SA071401
Intuitive Surgical, Inc. is recalling Intuitive brand da Vinci S, 5 mm Instrument Cannula Model/Part Number: 420011-02, Product is manufac due to Sharp Edges: the 5mm Cannula may have a sharp edge on the inner diameter of the Cannula. The defective cannulae may cause particulate shavings to be . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sharp Edges: the 5mm Cannula may have a sharp edge on the inner diameter of the Cannula. The defective cannulae may cause particulate shavings to be skive (scraping) from the instrument shafts during surgery.
Recommended Action
Per FDA guidance
On 11/19/07, the firm issued Urgent Device Recall Notification letters via Federal Express to all its direct consignees, informing them of the affected product and providing instructions on the recall.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AZ, CA, CT, GA, LA, MI, MN, NV, NJ, NC, OH, PA, SD, TX, VA, DC
Page updated: Jan 10, 2026