HUMAN MED AG 2025-03-12 Health serious FDA
Health · FDA · Recall #FDA-Z-1251-2025
human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107,… Recall
Issued March 12, 2025 · HUMAN MED AG
In March 2025, HUMAN MED AG recalled the human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact HUMAN MED AG to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- HUMAN MED AG
- Category
- Health
- Recall date
- March 12, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the state of FL.
- Recall number
- FDA-Z-1251-2025
- Made in
- Germany
- Issuing agency
- FDA
In context
- HUMAN MED AG has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.