[Recalled] 8mm Maryland Bipolar Forceps used in conjunction with the da Vinci Surgical System, Model IS1200. Multiple use electrosurgical endoscopic instruments. — Reports of dislodging of the Cautery Plug Insert from the Cautery Plug Ri
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | 8mm Maryland Bipolar Forceps used in conjunction with the da Vinci Surgical System, Model IS1200. Multiple use electrosurgical endoscopic instruments. |
|---|---|
| Brand / manufacturer | Intuitive Surgical, Inc. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1432-2013 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 08 May 2013 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Reports of dislodging of the Cautery Plug Insert from the Cautery Plug Riser, preventing a bipolar cautery cable from being properly connected which results in loss of cautery function of Bipolar Instruments.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Intuitive Surgical, Inc.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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