Bend, OR, United States
ReNovo, Inc. recalls
1 recall recorded since 2018, most recently on 19 January 2021. 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
- 19 January 2021
- Reason
- Non-sterile product was shipped to customers labelled as sterile.
- Distribution
- US Nationwide distribution in the states of CA, NJ and OR.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-1159-2021
- Various reprocessed products: PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO; PROVISION Reprocessed Depy Mitek Ablation Electrodes, VAPR COOLPULSE 90 deg; PROVISION Reprocessed Smith and Ne
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.