Schwerin, Germany
HUMAN MED AG recalls
1 recall recorded since 2018, most recently on 18 October 2024. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 18 October 2024
- Reason
- 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.
- Distribution
- US Nationwide distribution in the state of FL.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1251-2025
- human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.