Shannon, N/A, Ireland
ZIMMER ORTHOPEDIC MFG LTD recalls
1 recall recorded since 2018, most recently on 24 July 2017. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 24 July 2017
- Terminated
- 16 April 2018
- Reason
- There is a possibility that the protective foam insert used during the packaging of the affected products is undersized, which may cause a breach in the inner cavity during transportation.
- Distribution
- Worldwide Distribution - US Distribution to the states of : CA, MA, ME, MI, MN and WI., and to the countries of Germany, France and Italy.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0663-2018
- NexGen LPS Femoral Component, Left and Right, Size G Replaces the femoral condyle of the knee joint in Total Knee Arthroplasty.
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.