Intuitive Surgical, Inc. Intuiitve Surgical da Vinci 8 mm EndoWrist Curved Scissors, in box. All lots. P/N 400178-01 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Intuiitve Surgical da Vinci 8 mm EndoWrist Curved Scissors, in box. All lots. P/N 400178-01
Brand
Intuitive Surgical, Inc.
Lot Codes / Batch Numbers
FDA Device Listing Number R100529, Model Number 400178-01. 510(k) number K021036.
Products Sold
FDA Device Listing Number R100529, Model Number 400178-01. 510(k) number K021036.
Intuitive Surgical, Inc. is recalling Intuiitve Surgical da Vinci 8 mm EndoWrist Curved Scissors, in box. All lots. P/N 400178-01 due to Blades on the scissor may break and separate from the main unit as a result of corrosion damage.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Blades on the scissor may break and separate from the main unit as a result of corrosion damage.
Recommended Action
Per FDA guidance
The firm has sent notification letters to its consignees on 03/09/2005. Consignees are requested to return the feedback form provided by Intuitive Surgical, via Federal Express.
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 noticePage updated: Jan 10, 2026