[Recalled] human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use. — The cannula tubes do not comply with the specification | FDA 2024-10-18
A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.
Recall details
| Product | human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use. |
|---|---|
| Brand / manufacturer | HUMAN MED AG |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1251-2025 |
| Country of notice | Germany |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 18 October 2024 |
| EAN / barcode | 04260170881014 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: The cannula tubes do not comply with the specification. The water jet emerging from the nozzle of the nonconforming cannulas may emerge as a spot jet rather than a fan-shaped spray jet.
This Class II recall concerns device products distributed in Germany 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 →
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.