Galway, N/A, Ireland
Creganna Medical Devices recalls
1 recall recorded since 2018, most recently on 22 June 2023. 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
- 22 June 2023
- Reason
- Three lots of product may be labeled with an incorrect expiration day
- Distribution
- US Nationwide distribution in the state of AZ.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2249-2023
- Gore Tips Set Device, Catalog Number TSET1016, percutaneous liver access
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.