Tuttlingen, Germany
Smith & Nephew Orthopaedics GmbH recalls
1 recall recorded since 2018, most recently on 22 April 2022. 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 April 2022
- Reason
- Right nails were anodized, marked, and labelled as left nails and vice versa
- Distribution
- Distributed nationwide to GA, OH, IN, TX, CO, MO, TN, CA, NC, PA and internationally to Canada, Australia.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1133-2022
- INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Left INTERTAN 1.5 NAIL 13mm X 42cm 130DEG. Right
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.