Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098
FDA Recall Z-1518-2024 · Posted 2024-04-11
Advertisement
Reason for Recall
Firm Action
Root Cause
Nonconforming Material/Component
Distribution Pattern
US: VA, CA, NH, FL, NY, CO, AL, KY, MD, NC, NJ, OH, SC, SD, TN, WA, WI, WV, MS, TX, KS. OUS: China, France, Japan, South Korea
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.
Advertisement