Cheonan, N/A, Korea (the Republic of)
CORENTEC CO., LTD recalls
1 recall recorded since 2018, most recently on 29 March 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
- 29 March 2024
- Reason
- Due to unsupported 10 year expiration date.
- Distribution
- US Nationwide distribution in the states of AL, AZ, CA, MI, PA, TX.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-1934-2024, Z-1935-2024
- LOSPA Tibial Insert Model/Catalog Number: See below Software Version: N/A Product Description: Tibial Insert
- LOSPA Patella Component Model/Catalog Number: 01.10.9XX Software Version: N/A Product Description: Patella
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.