da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/ 00886874114605 ASSY,SSC,SP1098,P4/ 380940-44 / 00886874114735 ASSY,VSS,SP1098,P4/ 380941-44 / 00886874114742 SOFTWARE, SYSTEM EMBEDDED RLS, SP1098, B70_P4_B327 (OS4 v4.0.0 (P4_B327) / 610112-327 / N/A
Class I - DangerousWhat Should You Do?
- Check if you have this product: All da Vinci SP Surgical systems with software version OS4 v4.0.0 (P4_B327)
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Intuitive Surgical, Inc.
- Reason for Recall:
- Issue was identified during internal engineering evaluation. Use of the system with the affected software version may experience either an inability to deliver energy or an inadvertent delivery of energy. Use may require surgeon to resolve an injury or need moderate intraoperative intervention. Also, use may potentially cause user frustration or a minor delay to troubleshoot.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
da Vinci SP Surgical systems with the following Model Name/ Model Number / UDI: ASSY,PSS,SP1098,P4/ 380601-44/ 00886874114605 ASSY,SSC,SP1098,P4/ 380940-44 / 00886874114735 ASSY,VSS,SP1098,P4/ 380941-44 / 00886874114742 SOFTWARE, SYSTEM EMBEDDED RLS, SP1098, B70_P4_B327 (OS4 v4.0.0 (P4_B327) / 610112-327 / N/A
Product Codes/Lot Numbers:
All da Vinci SP Surgical systems with software version OS4 v4.0.0 (P4_B327)
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0419-2022
Related Recalls
Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
8MM,HORIZON SMALL CLIP APPLIER,IS4000¿ REF 470401
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.
8MM,MEGA SUTURECUT ND,IS4000 REF 471309
Intuitive Surgical
Due to increased complaints regarding frayed or broken grip cables on reusable instruments with jaws.