[Recalled] Valleylab Laparoscopic Flexible Laparoscopic Argon Blade Electrodes 28CM Item Code: E258028 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Valleylab Laparoscopic Flexible Laparoscopic Argon Blade Electrodes 28CM Item Code: E258028 The Valleylab Laparoscopic Handset and Electrodes are indicated for use in laparoscopic and thoracoscopic surgical procedures where the delivery of electrosurgical current, irrigation and suction via a sing |
|---|---|
| Brand / manufacturer | Medtronic |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2557-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 08 July 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential for compromise of the package resulting in a breach of the sterile barrier
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 Medtronic
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.