[Recalled] Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures. — Laparoscopic devices have a sterile symbol included on labels but devices are n… | FDA 2022-01-20
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | Product/Part: YelloPort Plus 5x70 Cannula + Luer/YC0507001. For use in laparoscopic procedures. |
|---|---|
| Brand / manufacturer | Surgical Innovations Ltd |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1853-2022 |
| Country of notice | United Kingdom |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 20 January 2022 |
| EAN / barcode | 05051986001890 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
This Class II recall concerns device products distributed in United Kingdom 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 Surgical Innovations Ltd
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.
- What is 2-ethoxyethyl acetate (CAS 111-15-9)? Safety, Regulation & EU/US/Canada Perspective | ProductGuru
- Top Rated Vitamins And Supplements
- How to Store Outdoor and Camping Gear Properly
- Biscuits and Sweet Snacks: A Buying Guide for Treat Lovers
- Comprehensive CPSC Product Safety Recalls Guide for Consumers
- Organic Imbiss Brands: A Healthier Choice for Today’s Conscious Consumers